Neet Practical Chemistry-Final

NEET (UG) SYLLABUS FOR PRACTICAL CHEMISTRY
2024 ONWARDS
Part A: Detection of Elements and Functional Groups
Detection of extra elements (Nitrogen, Sulphur, halogens) in organic
compounds.
Detection of the following functional groups: hydroxyl (alcoholic and
phenolic), carbonyl (aldehyde and ketones), carboxyl, and amino
groups in organic compounds.
Part B: Chemistry involved in the Preparation of Compounds
Inorganic Compounds: Mohr’s Salt, Potash Alum.
Organic Compounds: Acetanilide, p-nitro acetanilide, aniline yellow,
iodoform.
Part C: Chemistry involved in Titration
Acid base titration: Acids, bases and the use of indicators, Oxalic acid
vs KMnO₄, Mohr’s salt vs KMnO₄
Part D: Chemistry of Salt analysis
Cations: Pb2+, Cu2+, Al3+, Fe3+, Zn2+, Ni2+, Ca2+, Ba2+, Mg2+, NH4+.
Anions: CO32-, S2-, SO42-, NO3-, NO2-, Cl-, Br-, Mg2+, NH4+.
Part D: Chemical Principles involved in Experiments
1. Enthalpy of Solution of CuSO4.
2. Enthalpy of neutralisation of Strong acid and Strong base.
3. Preparation of lyophilic and lyophobic sols.
4. Kinetic study of the reaction of iodide ions with hydrogen
peroxide at room temperature.
***
TITRIMETRIC ANALYSIS
Y
OU are already aware that a substance is analysed to establish its qualitative
and quantitative chemical composition. Thus, chemical analysis can be
categorised as qualitative analysis and quantitative analysis. In this unit
you will learn about determination of the amount of substance in solution. Depending
upon the method adopted for determining the amount of chemical substances in
solution, there are two methods of analysis namely, titrimetric analysis and
gravimetric analysis. In titrimetric analysis measurement of only volumes is involved
while in gravimetric analysis measurement of volumes as well as mass is involved.
Titrimetric analysis involves determination of the volume of a solution of
accurately known concentration, which is required to react quantitatively with
the measured volume of the solution of a substance, concentration of which is to
be determined. The solution of accurately known concentration is called standard
solution. The mass of the substance dissolved in the solution of unknown
concentration is calculated from the volume of the standard solution used, the
chemical equation and the relative molecular masses of the reacting compounds.
The reagent of known concentration is called titrant and the substance being
titrated is termed as titrand.
To carry out titrimetric analysis, standard solution is usually added from
the long graduated tube called burette. The process of adding the standard
solution to the solution of unknown concentration until the reaction is just
complete is called titration. The point at which reaction is completed is called
equivalence point or the theoretical or stoichiometric end point. It is not
possible all the time to take standard solution in the burette. You will come to know
about it later in this unit in the titration of sodium hydroxide with oxalic acid.
6.1 DETECTION OF END POINT

The end point is detected either by some physical change produced in the reaction
mixture itself or by the addition of an auxiliary reagent, known as indicator;
alternatively some other physical measurement may be used. At the completion
of the reaction, the indicator shows a visible change e.g. (colour change or turbidity)
in the solution being titrated. In an ideal titration, the visible end point coincides
with the stoichiometric or theoretical end point; but in practice usually some
small difference occurs. This represents titration error.
Indicator and the experimental conditions selected should be such that the
difference between the visible end point and the theoretical end point is
minimum.Requirements for a Reaction in the Titrimetric Analysis
LABORATORY MANUAL CHEMISTRY
6.2 REQUIREMENT FOR A REACTION IN THE TITRIMETRIC ANALYSIS

(i) The substance of which amount is to be determined by
titrimetric analysis must react completely and rapidly with
the other reagent in stoichiometric proportion.
(ii) The reaction should be fast and there must be alteration in
physical or chemical property of the solution at the
equivalence point, which can be detected by an indicator, or
by measuring the potential difference or current etc.
6.3 ACIDIMETRY AND ALKALIMETRY

Titrimetric analysis can be carried out for various types of reactions.
In this unit you will learn only about neutralisation reactions.
These involve titrations of acids and bases. Standard solutions of
acids (acidimetry) and bases (alkalimetry) are used in these
titrations. In quantitative estimation through titrimetric analysis,
concentration of solution is expressed in terms of molarity. It is
number of moles of solute dissolved in 1 litre of solution.
number of moles of solute
Molarity, M =
volume of solution in litres
Standard Solution
A solution of exactly known concentration is called standard
solution. Any substance, which is stable at room temperature and
does not react with solvent in which it is dissolved, can be directly
weighed to prepare its standard solution. Description and
preparation of these solutions is given below:
Primary and secondary standards
A primary standard is a compound of sufficient purity in which
total amount of impurities does not exceed 0.01-0.02%. The
standard solution can be prepared by direct weighing of a sample
of primary standard followed by its dissolution in water (or solvent)
to obtain a definite volume of solution. The substance to be used as
a primary standard should also satisfy the following requirements:
1. It must be easily available in pure and dry form.
2. It should not undergo change in air i.e. it should not be
hygroscopic, oxidised by air or affected by gases such as
carbon dioxide present in the atmosphere or lose water of
crystallization, so that it can be stored safely.
3. It should be easy to detect the impurities present in it.
4. It should have high relative molecular mass so that weighing
errors are neglible.
5. Its reaction with another substance should be instantaneous
and stoichiometric.
6. The substance should be readily soluble in water.
66
It is difficult to obtain an ideal primary standard.

Therefore, substances having characteristics nearer to the
primary standards are usually employed.
Unstable hydrated salts, as a rule, should not to be used as
primary standards. However, sodium carbonate, sodium
tetraborate, potassium hydrogenphthalate, oxalic acid, ferrous
ammonium sulphate etc. can be used as primary standards
because of their sufficient stabilities.
A solution of secondary standard is the one which may be
used for standardization after finding out its exact concentration
by titration against a standard solution of primary standard.
A secondary standard cannot be used for preparing standard
solution by direct weighing. Sodium hydroxide and potassium
permanganate are examples of secondary standards.
Before starting titrimetric analysis, you should be familiar with
some techniques such as, weighing by using chemical balance,
preparing standard solution, measuring volume by using burette
and pipette.
6.4 INDICATORS IN ACID BASE TITRATION

Acid base indicators are sensitive to pH change. For most acid base
titrations, it is possible to select indicators which exhibit colour
change at pH close to the equivalence point. We will discuss here
about only two indicators – phenolphthalein and methyl orange.
Phenolpthalein
Phenolpthalein is a weak acid, therefore it does not dissociate in
the acidic medium and remains in the unionised form, which is
colourless.
HPh
H+ + Ph–

Unionised Ionised
Colourless Pink
Ionised and unionised forms of phenolphthalein are given below :
(Colourless in acid) (Pink in alkali)
Fig. 6.1 : Phenolphthalein in acidic and basic medium
67
In the acidic medium, equilibrium lies to the left. In the alkaline

medium, the ionisation of phenolphthalein increases considerably
+
due to the constant removal of H ions released from HPh by the
– –
OH ions from the alkali. So the concentration of Ph ion increases
in the solution, which imparts pink colour to the solution.
+ –
HPh
H + Ph
+ –
NaOH → Na + OH
+ –
H + OH → H2O
For a weak acid vs strong alkali titration, phenolphthalein is
the most suitable indicator. This is so because the last drop of
added alkali brings the pH of the solution in the range in which
phenolphthalein shows sharp colour change.
Methyl orange
Methyl orange is a weak base and is yellow in colour in the unionised
form. Sodium salt of methyl orange is represented as follows:
The anion formed from the indicator is an active species, which

on accepting a proton (i.e acting as Bronsted Lowry base) changes
from the benzenoid form to the quinonoid form. The quinonoid
form is deeper in colour and thus is responsible for the colour
change at the end point. This is illustrated in the following manner:
Benzenoid form of the anion Quinonoid form of the anion

(Yellow in colour) (Pinkish red in colour)
(Bronsted-Lowry base)
Fig. 6.2 : Structures of Methyl orange
Choice of Indicator
In the titration of strong acid and a weak base, methyl orange is
chosen as indicator. When titration between strong base and weak
acid is to be performed then phenolphthalein is a good indicator.
In this case alkali is dropped from the burette and acid is taken in
the tiration flask. Colour of the solution taken in the titration flask
68
changes from colourless to pink. This change of colour is easily

perceptible to the human eye. If we take alkali in the titration flask,
the colour change will be from pink to colourless and accuracy in
noting the colour change may be less. In the titration of strong
acid versus strong base anyone of the above indicators can be
used. For the titration of weak acid vs weak base no indicator is
available.
EXPERIMENT 6.1
Aim
Determination of the concentration (strength) of a given sodium
hydroxide solution by titrating it against a standard solution of
oxalic acid.
Theory
In the titration of a strong acid with a strong base, the amount of
acid and base becomes chemically equivalent at the end point and
the chemical reaction is called neutralization reaction. Near the
end point there is a sudden change in the pH of the solution. If
after end point even a small amount of base/acid is added the
solution would become slightly alkaline or acidic respectively. In
the titration between oxalic acid (weak acid) and sodium hydroxide
(strong base), following reaction takes place:
In this titration phenolphthalein (HPh) is used as an indicator.

The concentration of unknown solution is calculated in g/L.
Molarity of the solution can be calculated by using the formula
a1 M1 V1 = a2 M2 V2 ...(4)
where a1, M1, V1 are respectively basicity, molarity and volume

of acid used and a2, M2 and V2 are acidity, molarity and volume
respectively of base used in the titration.
69
Material Required
• Burette (50 mL) : One

• Pipette (10 mL) : One
• Oxalic acid : As per need
• Conical flask (100 mL) : One
• Sodium hydroxide
• Burette stand : One
solution : As per need
• Funnel : One
• Phenolphthalein
• White glazed tile : One indicator : As per need
• Measuring flask (100 mL) : One
Procedure
(A) Preparation of 0.1M Standard Solution of Oxalic Acid

Oxalic acid
Follow the procedure as described in Experiment No. 2.1.
Sodium Hydroxide
(B) Titration of Sodium Hydroxide and Oxalic Acid Solution
(i) Clean the burette thoroughly, wash it with distilled water

and finally rinse it with sodium hydroxide solution. (Always
rinse the burette (Fig. 2.17) with the solution, which is to be
taken in it). Clamp the burette vertically in a burette stand.
(ii) Fill sodium hydroxide solution into the burette through a
funnel above the zero mark.
(iii) Remove the air gap, if any, from the nozzle of the burette
by running the solution forcefully from the burette nozzle.
(iv) Remove the funnel before noting initial reading of the
burette. Also while noting the reading, see that no drop of
the liquid is hanging at the nozzle of the burette.
(v) Note the initial reading by keeping the eye exactly at the
same level as the meniscus of the solution.
(vi) Pipette out 10 mL of oxalic acid solution in a washed and
dried conical flask. Always wash the pipette with water and
rinse (Fig. 2.21) with the liquid to be measured before
pipetting out the liquid.
(vii) Add 1-2 drops of phenolphthalein indicator to the conical
flask. Place the flask over the glazed tile as shown in
Fig. 6.3 Titrate the acid with sodium hydroxide solution
till a very faint permanent pink colour is obtained. Add
sodium hydroxide solution in small amounts initially and
then dropwise.
70
Note : • Adjust the flow of liquid by the thumb and two

fingers held around the stop cock with a slight
inward pressure on the plug to prevent leakage.
• Swirl the liquid during the titration.
Fig. 6.3 : Titrating the solution
(viii) Read the lower meniscus of the solution in the burette again
and record it as final reading.
(ix) Repeat the procedure until three concordant readings are
obtained. Record your readings as in Table 6.1.
Table 6.1 : Titration of sodium hydroxide vs oxalic acid solution
Volume of oxalic Burette readings Volume of sodium

acid solution hydroxide solution Concordant
Sl. No. taken in conical Initial Final used reading in
flask each time reading reading V2 mL = (y–x) mL mL
V 1mL (x) (y)
71
Calculations
Molarity of NaOH solution can be calculated by using the equation:
Oxalic acid Sodium hydroxide
a1 M1V1 = a2 M2V2
where, M1 and V1 are the molarity and volume of the oxalic
acid solution.
M2 and V2 are the molarity and volume of the sodium hydroxide
solution.
a1 and a2 are respectively the basicity of oxalic acid and acidity
of sodium hydroxide. In this case a1= 2 and a2 = 1.
–1
Also, Molar mass of oxalic acid, (COOH) 2.2H2O = 126 g mol
–1
and Molar mass of sodium hydroxide (NaOH) = 40 g mol
Calculate the concentration of sodium hydroxide solution in g/L
by using the equation given below.
Concentration (strength) in g/L = Molarity×Molar mass
Result
Concentration of NaOH solution is ——————— g/L.
Precautions
(a) Always rinse the burette with the solution, which is to be taken in it.
(b) Remove the air gap if any, from the burette before titrating the solution. Make
sure that the nozzle of burette is also filled.
(c) Never forget to remove the funnel from the burette before noting the readings of
the burette and ensure that no drop is hanging from the nozzle of the burette.
(d) Always read the lower meniscus for all transparent solutions and upper meniscus
for coloured solutions.
(e) To note the burette readings place the eye exactly at the level of the meniscus.
(f) Never hold the pipette at the bulb.
(g) Never use the pipette and burette with a broken nozzle.
(h) Never suck a strong acid or an alkali with the pipette.
(i) Always keep the lower end of the pipette dipped in the liquid while sucking the
liquid.
(j) Do not blow out the last drop of the solution from the jet end of the pipette into
the flask.
(k) The concentration (strength) of the solution must be calculated up to the fourth
place of decimal.
72
Discussion Questions
(i) Why are the burette and the pipette rinsed with the solution with which these are filled?
(ii) What is an indicator? Which indicator is used in the titration of oxalic acid vs sodium
hydroxide? Can the titration be performed by using some other indicator?
(iii) Why should one read the lower meniscus in the case of colourless and transparent solutions
and the upper meniscus for solutions of dark colour?
(iv) Explain the term ‘end point’?
(v) What do you mean by 1.0 M solution?
(vi) Why should the last drop of the solution not be blown out of a pipette?
(vii) Explain the term basicity of an acid and acidity of a base?
(viii) For titrating NaOH vs HCl, phenolphthalein and methyl orange, both are suitable indicators.
Why?
(ix) What is meant by the term , ‘concordant readings’?
(x) Can one take oxalic acid solution in the burette and sodium hydroxide solution in the
titration flask? Point out the limitations of doing so if any.
KNOW THIS ALSO
The complete neutralisation is possible only when the amount of alkali is in equivalent
proportion to the amount of acid. Therefore, at the end point equivalent mass of acid dissolved
in volume V1 of solvent should be equal to the equivalent mass of the base dissolved in
Volume V2 of solvent. If N1 and N2 are equivalent masses of acid and base respectively dissolved
in per litre of solution then N1V1 = N2V2 … (i)
Equivalent mass of acids and bases is given by the following expression:
molar mass
Equivalent mass of acid = … (ii)
basicity
molar mass
Equivalent mass of base = ... (iii)
acidity
The number of gram equivalent mass of solute dissolved in one litre of the solution is
called the normality of the solution. For acids and bases
Number of gram equivalent mass w/ Equivalent mass
Normality (N)= = … (iv)
Volume of solution in litre (V ) Volume of solution in litre (V )
Where w = mass of substance in grams
Relationship between Normality and Molarity

From definition of normality (N) [(equation (iv)]
w
Equivalent mass = ... (v)
N ×V
If acidity or basicity is ‘a’, then by definition of equivalent mass
73
Molar mass
Equivalent mass = … (vi)
a
From equations (v) and (vi) we can write
w Molar mass
=
N ×V a
a (w/Molar mass )
Or N=
V
w/Molar mass
But is the molarity (M)
V
Therefore, N = a M … (vii)
Equation (vii) is the expression for the relationship between normality and molarity.
By using equation (vii) in equation (i) we have a1M1V1 = a2M2V2 .... (viii)
Where a1 and a2 are basicity and acidity of acid and base respectively and M1 and M2 are
the molar masses of acid and base respectively. Thus we see that equation (i) can also be
used to calculate the strength of the solution. Equation (viii) can be used for making the
solution by dilution. For solutions of the same substance a1 = a2. Therefore for using equation
(viii) for dilution of solution –
M1V1 = M2V2 ...(ix)
Therefore, to obtain V2 volume of a solution of molarity M2 from a solution of molarity M1,
the volume V1 of the solution of molarity M1 which is required for dilution, can be calculated
from equation (ix). (V2–V1) volume of solvent will be required to be added to V1 volume of the
solution of molarity M1.
EXPERIMENT 6.2
Aim
Preparation of (0.1 M) standard solution of sodium carbonate.
Theory
Sodium carbonate has characteristics nearer to the primary
standards therefore its standard solution can be made by direct
weighing.
To prepare 0.1 M Na2CO3 solution, 10.6000g of sodium
carbonate should be dissolved per litre of the solution (Molar mass
–1
of sodium carbonate is 106 g mol ).
Therefore, to prepare 100 mL of 0.1M Na2CO3 solution 1.0600 g
of sodium carbonate is dissolved in minimum quantity of water
and the solution is diluted to exactly 100 mL by adding water to it.
74
Material Required

• Watch glass : One
• Sodium carbonate : As per need
• Funnel : One
• Wash bottle : One
Procedure
Follow the same procedure as in Experiment 2.1.
EXPERIMENT 6.3
Aim
Determination of the strength of a given solution of dilute
hydrochloric acid by titrating it against a standard solution of sodium
carbonate.
Theory
The strength of hydrochloric acid is determined by titrating it against
a standard solution of sodium carbonate. The following reaction
takes place:
Na2CO3 + 2HCl → 2 NaCl + CO2 + H2O
In this titration, methyl orange, a weak base (yellow in the
unionised form) is used as an indicator.
In this experiment also, the titration follows the usual course,
i.e., the proton furnished by the addition of the acid first neutralises
sodium carbonate solution. When the entire sodium carbonate
solution is neutralised, the last drop of the acid added from the burette
produces the pinkish red colour change, which is the end point.
The concentration (strength) of the unknown solution is
calculated in g/L. It is calculated from the molarity of the solution.
Here, the molarity equation is written as
Base Acid
a1M1V1 = a2M2V2
where, a1 and a2 are the acidity and basicity of the alkali and the
acid respectively. M1 and M2 are the molarities, V1 and V2 are the
volumes of the base and acid respectively used to neutralise each
other.
75
Material Required

• Conical flask (100 mL) : One • Hydrochloric acid : As per need
• Burette stand : One • Sodium carbonate : As per need
• Funnel : One • Methyl orange solution : As per need
• Glazed tile (white) : One
Procedure
(A) Preparation of 0.1 M standard solution of sodium
carbonate
Hydrochloric acid
Follow the procedure as described in Experiment 2.1.
(B) Titration of hydrochloric acid and standard sodium
carbonate solution.
Follow the procedure as given in the Experiment 6.1.
In this case, hydrochloric acid is taken in the burette and
sodium carbonate solution in the conical flask. Methyl orange is
used as an indicator. The colour change at the end point will be
from yellow to pinkish-red. Record your observations in Table 6.2.
Table 6.2 : Titration of Hydrochloric acid with standard sodium carbonate solution
Volume V1 of Burette readings Volume of HCl

Na2CO3 solution solution used Concordant
Sl. No. taken in the Initial Final reading
conical flask reading reading V2 mL = (y–x) mL in mL
each time in mL (x) (y)
76
Calculations
Calculate the strength of HCl solution by using the equation
Na2CO3 solution HCl solution
a1M1V1 = a2M2V2
where M 1 and V1 are the molarity and volume of sodium carbonate solution
–
respectively and a1 is the number of moles of OH (aq) ions supplied by one
mole of the base (i.e. the acidity of the Na2CO3 solution).
∴ a1 = 2
M2 and V2 are the molarity and volume respectively of hydrochloric acid

solution.
+
a2 is the number of moles of H (aq) ions supplied by one mole of the acid
(i.e. the basicity of HCl).
∴ a2 = 1
–1 –1
Molar mass of Na2CO3 = 106 g mol , Molar mass of HCl = 36.5 g mol ,
∴ Concentration (Strength) of HCl solution in g/L = Molarity × Molar mass
Result
The concentration (strength) of the given HCl solution is _______g/L.
Precautions
(a) Care should be taken while handling the acid and base.
(b) Always rinse the burette and the pipette with the solution which is to be taken in
them.
(c) Remove the air gap if any, from the burette before titration.
(d) Never forget to remove the funnel from the burette before noting the initial reading
of the burette and ensure that no drop is hanging from the nozzle.
(e) Always read the lower meniscus for all transparent solutions and upper meniscus
for the coloured solutions.
(f) Never use burette and pipette with a broken nozzle.
(g) Never suck a strong acid or an alkali with the pipette, use pipette bulb.
(h) Always keep the lower end of the pipette dipped in the liquid while sucking the
liquid.
(i) While transferring the solution to the flask, do not blow out the last drop of the
solution from the jet of the pipette.
(j) The strength of the solution must be calculated up to the fourth decimal place.
77
KNOW THIS ALSO
Potassium hydrogenphthalate is primary standard for standardisation of sodium hydroxide

solution. Formula of potassium hydrogen phthalate is C6H5O4K. It behaves as a monobasic
acid. Sodium hydroxide reacts with potassium hydrogenphthalate according to the following
equation.
Phenolphthalein can be used as an indicator in this titration.
(i) Which indicator is used in the titration of sodium carbonate against hydrochloric acid and
what is the colour change at the end point?
(ii) How will you prepare 250 mL of 0.05 M solution of sodium carbonate?
(iii) Though sodium carbonate is a salt yet its aqueous solution is weakly alkaline in nature.
Explain why?
(iv) How can you determine the acidity of sodium carbonate solution?
(v) Why is methyl orange not an Arrhenius base?
(vi) How can you titrate a solution of the mixture of Na2CO3 and NaHCO3 against HCl?
(vii) What is the difference between an end point and an equivalence point?
(viii) Can you directly prepare standard solution of HCl, HNO3 and H2SO4 ?
78
UNIT-1
COLLOIDS
I
N a true solution, solute particles mix homogeneously with the molecules of
the solvent and thus form a single phase. However, a colloidal solution is a
heterogeneous system in which very fine particles of one substance disperse
(dispersed phase) in another substance called dispersion medium. Particles
of the dispersed phase do not form a single phase with the particles of the
dispersion medium because of the fact that they are either very large molecules
or essentially aggregates of small molecules. Colloidal particles are larger in size
than simple molecules but small enough to remain suspended in the dispersion
–9 –6
medium (10 –10 m). Some examples of very large molecules which form collidal
dispersion are starch, gum and proteins, whereas colloidal sulphur is an example
of aggregates of small molecules. Further, a heterogeneous system of a solid as
dispersed phase and a liquid as dispersion medium is called a sol. Depending
upon the nature of interaction between the dispersed phase and the dispersion
medium, colloidal sols are divided into two categories, namely, lyophilic (solvent
attracting) and lyophobic (solvent repelling). If water is the dispersion medium,
the terms used are hydrophilic and hydrophobic. Egg albumin, starch and gum
are lyophilic sols. Freshly prepared ferric hydroxide, aluminium hydroxide and
arsenic sulphide sols are examples of lyophobic sols. A few methods of
preparation of colloids are – chemical methods, electrical disintegration and
peptization. In this unit you will learn to prepare both the types of sols. Also, you
will learn a method of purification of sols.
EXPERIMENT 1.1
Aim
To prepare (a) lyophilic sol; and (b) lyophobic sol.
Theory
Since particles of dispersed phase in lyophilic sols have an affinity for the particles
of dispersion medium, these sols are more stable as compared to lyophobic sols.
Two factors responsible for the stability of sols are – charge and the solvation of
the colloidal particles by the solvent. Stability of lyophilic sols is primarily due to
the solvation of colloidal particles by the solvent whereas lyophobic sols are
stabilised by the charge on the colloidal particles. Due to their charges, colloidal
particles remain suspended in solution and coagulation does

not take place. These charges may be positive or negative.
Some examples of negatively charged sols are starch and arsenious
sulphide. Positively charged sol of hydrated ferric oxide is formed
when FeCl3 is added to excess of hot water and a negatively charged
sol of hydrated ferric oxide is formed when ferric chloride is added
to NaOH solution. The lyophilic sols are directly formed by mixing
and shaking the substance with a suitable liquid. Lyophobic sols
cannot be prepared by direct mixing and shaking. Special methods
are employed to prepare these.
Material Required
• Beaker (250 mL) : One

• Egg : One
• Watch glass : One
• Sodium chloride : 5g
• Porcelain dish : One
• Ferric chloride : 2g
• Measuring cylinder : One
• Aluminium chloride : 2g
(100 mL)
• Starch/gum : 500 mg
• Arsenious oxide : 0.2 g
• Graduated pipette : One
(20 mL)
Procedure
A. Preparation of Lyophilic Sol
Aluminium
I. Egg Albumin Sol
chloride (i) Prepare 100 mL of 5% (w/v) solution of NaCl in water in
a 250 mL beaker.
Arsenic
compounds (ii) Break one egg in a porcelain dish and pipette out the
albumin and pour it in sodium chloride solution.
Stir well to ensure that the sol is well prepared.
Hazard Warning
II. Starch/gum Sol
• While doing experiment (i) Measure 100 mL of distilled water with the help of a
do not eat, drink or
measuring cylinder and transfer it to a 250 mL beaker
smoke.
and boil it.
(ii) Make a paste of 500 mg starch or gum in hot water
and transfer this paste to 100 mL of boiling water with
constant stirring. Keep water boiling and stirring for
10 minutes after addition of paste. To judge the efficacy
of the prepared sol, you may compare it with the
original paste prepared.
B. Preparation of Lyophobic Sol
I. Ferric hydroxide/Aluminium hydroxide
(i) Take 100 mL of distilled water in a 250 mL beaker and
boil it.
2
COLLOIDS
(ii) Add 2g of ferric chloride/aluminium chloride powder to

boiling water and stir it well.
(iii) Take 100 mL of distilled water in another 250 mL beaker
and boil it.
(iv) Pour 10 mL of ferric chloride/aluminium chloride solution
prepared in step (ii) drop by drop into the boiling water
with constant stirring. Keep the water boiling till brown/
white sol is obtained.
II. Arsenious Sulphide Sol
(i) Transfer 100 mL of distilled water to a beaker of 250 mL
capacity.
(ii) Add 0.2 g of arsenious oxide to it and boil the content of
the beaker.
(iii) Cool and filter the solution.
(iv) Pass hydrogen sulphide (H2S) gas through the filtered
solution till it smells of H2S. (Use Kipp’s apparatus to
pass hydrogen sulphide gas).
(v) Expel H2S gas from the sol by slow heating and filter it.
(vi) Label the filtrate as arsenious sulphide sol.
Precautions
(a) While preparing colloidal solutions of starch, gum, ferric chloride, aluminium
chloride etc., pour the paste or solution gradually into the boiling water with
constant stirring. Addition of these substances in excess may cause precipitation.
(b) Arsenious oxide is poisonous in nature; so wash your hands immediately every
time after handling this chemical.
(i) How will you differentiate between a true solution and a colloidal dispersion?
(ii) Identify some sols (colloids) that you use in your daily life and mention their importance.
(iii) How do colloids acquire a charge? Why is ferric hydroxide/aluminium hydroxide sol
prepared in the experiment, positively charged while arsenious sulphide sol is negatively
charged?
(iv) What is coagulation? How is coagulation different from peptization?
(v) How can you convert a colloidal dispersion of sulphur into a true solution?
(vi) Out of lyophilic and lyophobic sols, which one can be easily converted into a gel and why?
(vii) Differentiate between a gel and a sol.
(viii) What are the applications of colloids in the field of Medicine, Defense and in Rocket Technology?
3
EXPERIMENT 1.2
Aim
To purify prepared sol by dialysis.
Material Required
• Parchment/
cellophane paper : One sheet • Colloidal dispersion of : Prepared in
egg albumin experiment 1.1
(30 cm × 30 cm)
• Distilled water : As per requirement
• Trough : One
• Uranyl zinc acetate : As per requirement
• Thread : As per need
• Silver nitrate : As per requirement
• Test tubes : Two
Procedure
(i) Take a square sheet (30 cm × 30 cm) of parchment/
cellophane paper.
(ii) Soak the sheet in water and give it a conical shape.
(iii) Pour the colloidal dispersion of egg albumin in the cone of
parchment/cellophane paper.
(iv) Tie the cone with a thread and suspend it in a trough
containing distilled water as shown in Fig. 1.1.
Fig. 1.1 : Purification of a colloid
(v) After about half an hour, test for the presence of ions in the
trough water.
4
COLLOIDS
(vi) Change the water present in the trough after every half an
+ –
hour till it is free of the impurities of Na and Cl ions.
+ –
To check the presence of Na and Cl ions take water from
the trough in two test tubes. To one test tube add uranyl
zinc acetate and to the other add silver nitrate solution.
A yellow precipitate with uranyl zinc acetate indicates the
+
presence of Na ions, while a white precipitate of silver nitrate
indicates the presence of chloride ions.
(vii) Note the time required for the purification of colloidal dispersion.
Note : In some cases, dialysis may be a very slow process. Therefore, in such
cases, it is advisable to change the water of the trough twice or thrice
till the colloidal dispersion is free of ions.
Precautions
(a) For dialysis make the parchment bag air tight to prevent the entry of water into
the bag. Keep the neck of the parchment bag above the surface of water.
(b) Change the water in the trough from time to time during dialysis.
Discussion Question
(i) How can you make the process of dialysis quick? What are the limitations of this technique?
EXPERIMENT 1.3
Aim
To study the role of emulsifying agents in stabilising the emulsions
of different oils.
Theory
Emulsion is a type of colloid in which, both the dispersed phase
and the dispersion medium are liquids. Here the dispersed phase
and the dispersion medium are distinguished by their relative
amounts. The one, which is present in smaller proportion, is called
dispersed phase, while the other, which is present in relatively
large quantity, is known as the dispersion medium.
When oil is shaken with water, a faint milky solution is often
observed, which is unstable and is called an emulsion of oil in
water. On standing, it gets separated into two layers, i.e. oil and
5
water. The mixing capacity of different oils with water is different.

This mixing capacity of the oil in addition to its nature depends
upon the method of shaking also (i.e.vigorous shaking or swirling).
The stability of an oil and water emulsion is increased by the
addition of a suitable emulsifying agent such as soap solution.
Soap contains sodium salt of long chain aliphatic carboxylic acids
with the carboxyl group as the polar group, which decreases the
interfacial surface tension between oil and water. Hence oil mixes
with water and emulsification takes place. The concentration of
soap required for complete emulsification is called optimum
concentration. Any amount less or more than this optimum
amount does not cause an effective stabilisation. In the presence
of optimum amount of soap solution, oil in water emulsion is more
stable and the separation of oil and water layers takes more time.
Material Required
• Test tubes : Six • Soap/detergent : 5g

• Droppers : Five • Mustard oil,
• Test tube stand : One linseed oil,
• Glass rod : One castor oil and : 10 mL each
• Stop watch : One machine oil brand
Procedure
(i) Dissolve 1 g of soap/detergent in 10 mL of distilled water in
a test tube with vigorous shaking and heat the content of
the test tube if needed. Label it as ‘A’.
(ii) Take four test tubes. Mark these as B, C, D and E and to
each of the test tubes, add 5 mL distilled water followed by
10 drops of mustard oil in test tube B, linseed oil in test tube
C, castor oil in test tube D and machine oil in test tube E,
respectively.
(iii) Shake test tube B vigorously for five minutes, keep it in a
test tube stand and simultaneously start the stopwatch.
Record the time taken for the separation of the two layers.
(iv) Repeat the same procedure with test tubes C, D and E and
record the time for the separation of the layers in each case.
(v) Now add two drops of soap/detergent solution from test
tube ‘A’ into each test tube (B, C, D and E). Shake each test
tube for five minutes and record the time of separation of
the layers in each case again.
(vi) Record your observations in a manner detailed in
Table 1.1.
6
COLLOIDS
Table 1.1 : Emulsification of different oils by soap/detergent
Test tube Name of oil used for Time taken for the
specification emulsification separation of layers
Without Soap/ With Soap/
detergent detergent
Precautions
(a) Add equal number of drops of a soap/detergent solution to all the test tubes.
(b) To minimise the error in recording the time required for the separation of layers
in different systems, shake all the test tubes for identical time span.
(c) Start the stopwatch immediately after shaking is stopped and stop it immediately
when the two layers separate.
(i) Name a reagent other than soap, which can be used as an emulsifying agent in the oil in
water type emulsion.
(ii) Milk is said to be a stable emulsion. What provides stability to milk?
(iii) Can two miscible liquids form an emulsion?
(iv) Why do separation of layers of different oils forming an emulsion with water take different
time?
(v) What are the points of similarity and dissimilarity among sol, gel and emulsion?
(vi) Suggest a test to distinguish between Oil in Water and Water in Oil type of emulsions.
(vii) Give some examples of emulsions that you come across in daily life.
(viii) Dettol forms an emulsion in water. How does this emulsion get stabilised?
7
UNIT-2
CHEMICAL KINETICS
R
ATE of reaction can be measured either in terms of decrease in concentration
of any one of the reactants or increase in concentration of any one of the
products with time. For a hypothetical reaction,
A → B
∆[A] ∆[B]
Rate of reaction = − =
∆T ∆T
Factors such as concentration, temperature and catalyst affect the rate of a
reaction. In this unit you will learn the technique of determining the rate of a
reaction and technique of studying the effect of concentration and temperature
on the reaction rate.
EXPERIMENT 2.1
Aim
To study the effect of concentration and temperature variation respectively on
the rate of reaction between sodium thiosulphate and hydrochloric acid.
Theory
Sodium thiosulphate reacts with hydrochloric acid and produces a colloidal
solution of sulphur, which makes the solution translucent. The reaction occurs
as follows:
Na2S2O3 (aq) + 2HCl (aq) → 2NaCl (aq) + H2O(l) + SO2 (g) + S(s)
Ionic form of the above reaction is written as:
2– +
S2 O3 (aq) + 2H (aq) → H2O (l) + SO2 (g) + S(s)
The property of the colloidal solution of sulphur to make the system
translucent is used to study the rate of precipitation of sulphur. The rate of
precipitation of sulphur increases with an increase in the concentration of the
reacting species or with an increase in the temperature of the system. With an
increase in the concentration, the number of molecular collisions per unit time
between the reacting species increase and consequently chances of product
formation increase. This results in an increase in the rate of precipitation of
sulphur. Similarly, on increasing the temperature, the kinetic energy of the
reacting species increases, so the number of collisions that result in the formation
of products increase leading to a faster rate of reaction.
CHEMICAL KINETICS
Material Required

• Pipette (25 mL) : One • 0.1M Sodium
• Pipette(5 mL) : One thiosulphate : As per need
• Burette stand : One • 1.0 M Hydrochloric
• Stop watch : One acid : As per need
• Thermometer (110°C) : One
Procedure
A. The effect of concentration on the rate of reaction
(i) Take a trough and fill half of it with water. This will serve as
constant temperature bath, maintained at room temperature. Hydrochloric acid
(ii) Rinse and fill the burette with 1.0 M HCl solution.
(iii) Take a 100 mL beaker and make a mark ‘X’ in the centre
of the outer surface of the bottom with the help of a glass
marker pencil. Fill 50 mL of 0.1M sodium thiosulphate
solution in it. Place the beaker in the trough. The mark ‘X’
will be visible to the naked eye on account of the
transparent nature of the system. Allow the beaker to stand
in the trough for a few minutes so that it attains the
temperature of the bath.
(iv) Add 1.0 mL of 1.0 M HCl solution with the help of a burette.
Start the stopwatch when half the HCl solution i.e. (0.5 mL)
has been transferred. Swirl the beaker while adding HCl.
(v) Record the time required for the mark ‘X’ on the bottom of
the beaker to become invisible (This is considered as a stage
of completion of the reaction).
(vi) Repeat the experiment by adding 2 mL, 4 mL, 8 mL and 16
mL of 1.0 M hydrochloric acid solution to fresh sodium
thiosulphate solution every time and record the time required
for the disappearance of the mark ‘X’ in each case separately.
B. The effect of temperature on the rate of reaction
(i) Take 50 mL of 0.1M sodium thiosulphate solution in a
100 mL beaker, on the outer surface of the bottom of which
a mark ‘X’ has been made. Keep the beaker in a thermostat
maintained at 30°C. Add 5 mL of 1.0 M hydrochloric acid
solution with swirling. Start the stopwatch immediately
when half the amount (i.e. 2.5 mL) of hydrochloric acid
has been transferred.
(ii) Record the time at which the mark ‘X’ becomes invisible.
(iii) Repeat the experiment at temperatures 40°C, 50°C, 60°C
and 70°C using fresh sodium thiosulphate solution each
9
time and record the time required for the disappearance of

the mark ‘X’.
(iv) Record your observations in Tables 2.1 and 2.2.
(v) Plot two graphs, one for the volume of HCl added (which
determines concentration of HCl) and the time taken for the
mark to become invisible and the other between temperature
and the time taken for the mark to become invisible. For plotting
the graph, the variation in time is plotted on x-axis and the
variation in volume or temperature is plotted on y-axis.
Note : If thermostat (i.e. constant temperature bath) is not available for

studying the rate of the reaction. Ordinary water bath may also
be used for maintaining constant temperature but in this case
heating of the bath from outside might be required for the
adjustment of temperature. Water in the bath should also be stirred
continuously.
Table 2.1 : Effect of concentration of HCl on the rate of reaction between

sodium thiosulphate and hydrochloric acid
Amount of Na2S2O3 solution used each time = 50 mL
Concentration of Na2S2O3 solution = 0.1M, Room temperature = °C
Concentration of the HCl solution used in the reaction mixture = 1.0 M
Volume of HCl added in mL Time ‘t’ in seconds for the mark

Sl. No.
‘X’ to become invisible
1. 1.0
2. 2.0
3. 4.0
4. 8.0
5. 16.0
Table 2.2 : The effect of temperature on the rate of reaction between

sodium thiosulphate and hydrochloric acid
Volume of sodium thiosulphate solution used each time = 50 mL
Volume of HCl used each time = 5 mL
Temperature of the reaction Time ‘t’ in seconds for the mark
Sl. No. mixture/°C ‘X’ to become invisible
1. 30
2. 40
3. 50
4. 60
5. 70
Result
Write your conclusions on the basis of data in Tables 2.1 and 2.2.
10
CHEMICAL KINETICS
Precautions
(a) Start the stopwatch when half of the hydrochloric acid solution has been
transferred to the reaction flask and stop the watch when the mark ‘X’ becomes
invisible.
(b) If a constant temperature bath is not available to maintain the constant
temperature, heat the water of the bath in which the beaker is kept from time to
time with constant stirring, and remove the burner when the required temperature
is attained.
(c) Select suitable scale for plotting the graph.
(i) The reaction under examination is as follows:

2– +
S2 O3 (aq) + 2H (aq) → H2O (l) + SO2 (g) + S(s)
Write the conditions under which the rate law expression for this reaction can be written in
the following manner.
2– + 2
Rate of precipitation of sulphur = k [S2O3 ][H ]
(ii) Suppose the above rate law expression for the precipitation of sulphur holds good, then
2– +
on doubling the concentration of S2 O3 ion and H ion, by how many times will the rate of
the reaction increase?
(iii) Comment on the statement that for a given reaction, rate of the reaction varies but the rate
constant remains constant at a particular temperature.
(iv) How does the rate constant of a reaction vary with temperature?
(v) Devise an experiment to study the dependence of rate of precipitation of sulphur upon the
nature of monobasic acid for the reaction given below :
2– +
S2O3 (aq) + 2H (aq) → H2O (l) + SO2 (g) + S(s)
(vi) Why is the stop watch/stop clock started when half of the reactant is delivered into the
beaker?
2–
(vii) The structure of S2 O3 ion is described as follows:
11
The two sulphur atoms are marked here as (1) and (2). Which
of the sulphur atoms, according to you, is precipitated as
colloidal sulphur? How can you verify your answer
experimentally?
(viii) What is the difference between the order and the molecularity
of a reaction?
(ix) The molecularity of a reaction can’t be zero but the order
can be zero? Explain.
(x) Can the order of a reaction be a fractional quantity?
(xi) Suppose the above reaction follows third order kinetics, then
in what units, will the rate of the reaction and the rate
constant be expressed?
EXPERIMENT 2.2
Aim
To study the effect of variation in concentration of iodide ions on
the rate of reaction of iodide ions with hydrogen peroxide at room
temperature.
Theory
The reaction between iodide ions and hydrogen peroxide occurs
in the acidic medium and can be represented in the following
manner:
– +
2I (aq) + H2O2 (l) + 2H (aq) → I2(g) + 2H2O (l)
–
In this reaction, hydrogen peroxide oxidises iodide ions (I ) to
molecular iodine. If calculated amount of sodium thiosulphate is
added in the presence of starch solution as an indicator to the above
reaction mixture, the liberated iodine reacts with thiosulphate ions
as fast as it is formed and is reduced back to iodide ions till all the
thiosulphate ions are oxidised to tetrathionate ions.
2– 2– –
I2(g) + 2S2O3 (aq) → S4O6 (aq) + 2I (aq)
After the complete consumption of thiosulphate ions, the
concentration of iodine liberated in the reaction of hydrogen
peroxide with iodide ions increases rapidly to a point where iodine
forms intense blue complex with starch. The time required to
consume a fixed amount of the thiosulphate ions is reproducible.
Since the time for the appearance of colour is noted, the reaction
is some times called a clock reaction.
12
CHEMICAL KINETICS
Material Required
• Starch solution : As per need

• 2.5 M Sulphuric acid
• Conical flasks (250 mL) : Five solution : As per need
• Conical flask (500 mL) : One • 0.1 M Potassium
• Stop watch : One iodide solution : As per need
• Measuring cylinder (100 mL) : One • 0.04M Sodium
• Trough : One thiosulphate solution : As per need
• 3% Hydrogen
peroxide solution : As per need
Procedure
(i) Take 25 mL of 3% hydrogen peroxide, 25 mL of 2.5 M H2SO4
Sulphuric acid
solution, 5 mL of freshly prepared starch solution and 195
mL distilled water into a 500 mL conical flask marked as A.
Stir this solution well and place it in a water bath maintained Hydrogen peroxide
at room temperature.
(ii) Take four 250 mL conical flasks and mark them as B, C, D and E.
(iii) Take the sodium thiosulphate solution, potassium iodide Hazard Warning
solution, and distilled water in the flasks B, C and D in a • Cotact of hydrogen-
proportion given in the following steps and keep the flask E peroxide with combustible
for carrying out the reaction. material may cause fire.
(iv) Take 10 mL of 0.04 M sodium thiosulphate solution, 10 mL
of 0.1 M potassium iodide solution and 80 mL of distilled
water in the conical flask marked B. Shake the contents of
the flask well and keep it in a water bath.
(v) Take 10 mL of 0.04 M sodium thiosulphate solution, 20 mL
of 0.1M potassium iodide solution and 70 mL of distilled water
in the conical flask marked C. Shake the resulting solution
well and place it in the same water bath in which reaction
mixture of step (iv) is kept.
(vi) Take 10 mL of 0.04 M sodium thiosulphate solution, 30 mL
of 0.1 M potassium iodide solution and 60 mL of distilled
water in the conical flask marked D. Shake the solution well
and keep this flask also in the above water bath.
(vii) Take conical flask E. Pour 25 mL solution from flask A into
it after measuring it with the help of a measuring cylinder.
Now add 25 mL of solution from flask B into this flask with
constant stirring. Start the stop watch when half of the
solution from flask B has been transferred. Keep the flask E
in a water bath to maintain the constant temperature and
record the time required for the appearance of blue colour.
(viii) In exactly the same manner, repeat the experiment with the
solutions of flasks C and D separately by using once again
25 mL of the solution of these flasks and 25 mL of solution
13
from flask A. Note the time required for the appearance of

blue colour in each case.
(ix) Repeat the experiment with solutions of flasks B, C and D
twice and calculate the average time for the appearance of
blue colour.
(x) Record your observations as given in Table 2.3.
(xi) Compare the time required for the appearance of blue colour
for all the three systems and make a generalisation about
the variation in the rate of the reaction with concentration of
iodide ions.
Table 2.3 : Study of reaction rate between iodide ions and
hydrogen peroxide in acidic medium
Sl. Composition of the Time taken for appearance of the

blue colour Average
No. system Time
First reading Second reading
1. 25 mL solution from flask A +

25 mL solution from flask B

25 mL solution from flask C

25 mL solution from flask D
Result
Write your conclusions on the basis of the data recorded in Table 2.3.
Precautions
(a) Always keep the concentration of sodium thiosulphate solution less than that of
potassium iodide solution.
(b) Always use freshly prepared starch solution.
(c) Use fresh samples of hydrogen peroxide and potassium iodide.
(d) Always use the same measuring cylinders for measuring solutions in two different
sets of observations. If after measuring one solution, the cylinder is used for
measuring another solution, clean it before using.
(e) Record the time immediately after the appearance of blue colour.
(i) Distinguish between the role of iodine and iodide ions in this experiment.
2–
(ii) Calculate the oxidation number of sulphur in tetrathionate ion (S4O6 ). Can the oxidation
number be a fractional number?
14
CHEMICAL KINETICS
(iii) Why does iodine impart blue colour to starch?

(iv) Explore the possibility of using an oxidant other than H2O2 in this experiment.
(v) Why is the reaction given the name clock reaction?
(vi) Why should the concentration of sodium thiosulphate solution taken be always less than
that of potassium iodide solution?
EXPERIMENT 2.3
Aim
To study the rate of reaction between potassium iodate (KIO3) and
sodium sulphite (Na2SO3).
Theory
The reaction between KIO3 and Na2SO3 indirectly involves the
formation of iodide ions, which are oxidised in acidic medium by
–
IO3 ions to iodine. The overall reaction proceeds in the following
two steps.
– 2– – 2–
IO 3 + 3SO3 → I + 3SO 4 (1)
– + –
5I + 6H + IO 3 → 3H2O + 3I2 (2)
The evolved iodine produces blue colour with the starch

solution in a manner described in the previous experiment.
This reaction like the earlier reaction is also known as ‘clock
reaction’.
Material Required
• 2 M Sulphuric acid : As per requirement

• Conical flasks (250 mL) : Six • 5% Starch solution : As per requirement
• Measuring • 6% Potassium iodate
cylinder (100 mL) : One solution : As per requirement
• Stopwatch : One • 6% Sodium sulphite
• Trough : One solution : As per requirement
15
Procedure
(i) Take a 250 mL conical flask and mark it as ‘A’. Transfer
25 mL of 6% potassium iodate solution, 25 mL of 2.0 M H2SO4
and 50 mL of distilled water into it and shake the content of
the flask well. Keep the flask in a trough half filled with water.
This serves as constant temperature bath.
(ii) Take five 250 mL conical flasks and mark these as B, C, D, E
and F respectively. Take 6% sodium sulphite solution, starch
solution and distilled water in flasks B, C, D and E in the
proportion given in the following steps and keep flask F for
carrying out the reaction.
(iii) In the conical flask marked ‘B’ take 20 mL of sodium sulphite
Note : solution, 5 mL of starch solution and 75 mL of distilled water.
• Total amount of Shake the contents of the flask well and keep it in the water
solution in each bath.
flask is 100 mL
(iv) In the conical flask marked ‘C’, take 15 mL of sodium sulphite
• Same amount of solution, 5 mL of starch solution and 80 mL of distilled water.
indicator has been
Shake the resulting solution well and keep it in the water bath.
used.
(v) In conical flask ‘D’, take 10 mL of sodium sulphite solution,
5 mL of starch solution and 85 mL of distilled water. Shake
the solution well and place the flask in the water bath.
Sulphuric acid (vi) In conical flask ‘E’, take 5 mL of sodium sulphite solution,
5 mL of starch solution and 90 mL of distilled water. Shake
the content of the flask well and keep it in the water bath.
(vii) Take conical flask ‘F’. In this flask pour 25 mL of the solution
from the conical flask marked ‘A’ and add 25 mL of the solution
from the conical flask marked ‘B’. Start the stop watch when
half of the solution from flask B has been added. Mix these
two solutions thoroughly by constant stirring and keep it in
the water bath. Record the time required for the appearance of
blue colour (you may use stop watch/wrist watch for noting
the time).
(viii) In a similar manner, repeat the experiment with the solutions
in flasks C, D and E respectively by using 25 mL of the
solution as in the experiment with solution from flask B and
record the time required for the appearance of blue colour in
each case.
(Once again care should be taken to repeat the experiment for
each case twice so as to take the average time required for the
appearance of blue colour in each set).
16
CHEMICAL KINETICS
(ix) Record your observations as given in Table 2.4.

(x) From the tabulated results, find out the relationship between
the time of appearance of blue colour and the variation in
concentration of sodium sulphite.
Table 2.4 : Study of the reaction rate between potassium iodate (KIO3)
and sodium sulphite (Na2SO3) in acidic medium
Sl. Time taken for appearance of the Average

Composition of the
No. blue colour in seconds Times/
system
First reading Second reading sec.

25 mL solution from flask B
25 mL solution from flask C
25 mL solution from flask D

25 mL solution from flask E
Result
Write your conclusions on the basis of data recorded in Table 2.4.
Precautions
(a) As sodium sulphite is likely to be easily oxidised in air, therefore, always use its
fresh solution.
(b) Keep the concentration of potassium iodate solution higher than the concentration
of sodium sulphite solution.
(c) Use a freshly prepared starch solution.
(d) Start the stop watch when half of the solution from conical flask B, C, D or E is
added to the conical flask F containing 25 mL solution from flask A.
(i) How would the time for the appearance of blue colour vary if the temperature of the
experiment in the above case is enhanced by 10°C ?
(ii) Mention the factors that affect the rate of reaction in the present study.
17
(iii) Which of the acids, hydrochloric or nitric, would be suitable to make the medium acidic in
this experiment? Explain your answer with reasons.
(iv) Out of the reactions (1) and (2) given below:

– 2– – 2–
IO 3 + 3SO3 → I + 3SO 4 (1)
– – +
5I + IO 3 + 6H → 3H2O + 3I2 (2)
which could be the rate determining reaction? What is the molecularity of the rate
determining reaction?
3– 2–
(v) Can AsO3 be used in place of SO3 in the above reaction? Support your answer with
proper reasoning.
(vi) Why is the concentration of potassium iodate solution kept higher than the concentration
of sodium sulphite solution?
18
UNIT-3
THERMOCHEMICAL
MEASUREMENT
M
OST of the reactions are carried out at atmospheric pressure, hence
heat changes noted for these reactions are enthalpy changes. Enthalpy
changes are directly related to the temperature changes by the relation:
∆H = qp
= mCp ∆T
= VdCp ∆T ... (1)
where V = Volume of the solution.
d = Density of the solution
Cp = Heat capacity
∆T = Change in temperature
Measurement of heat changes are carried out in vessels called calorimeters.
Reactions may also be carried out in beakers placed in thermos flask or in
thermally insulated box or in styrofoam cup. Metallic calorimeters are not used
for measuring thermochemical changes because metals may react with
substances. Stainless steel or gold plated copper calorimeters may be used.
During measurement of heat changes, calorimeter, thermometer and stirrer also
absorb some heat; this amount of heat should also be known. It is called
calorimeter constant. In the case of a glass vessel, (e.g. beaker) calorimeter
constant for that part is found, which is actually in contact with the reaction
mixture. This is so because when thermal conductivity of the material of
calorimeter is low, only the area of the calorimeter in contact with the liquid
absorbs maximum heat. Method of mixtures is used to determine the calorimeter
constant. To determine calorimeter constant, known volume of hot water at a
specified temperature is added to known volume of water contained in the
calorimeter at room temperature. Since energy is conserved, the heat taken by
calorimeter and cold water should be equal to heat given by hot water. Thus, we
can write the following equation :
∆H1 + ∆H2 = –∆H3 ... (2)
Enthalpy change Enthalpy Enthalpy
of calorimeter, change of change of
stirrer and cold water hot water
thermometer
Let tc, th and tm be temperatures of cold water, hot water and mixture
respectively. Then, in view of the definition of enthalpy change given in equation
(1) we can rewrite equation (2) as
m1 C p1 (tm–tc) + m2Cp(tm–tc) + m3Cp (tm–th) = 0 ... (3)
where m1, m2 and m3 are masses of calorimeter, cold water and

hot water respectively and C p1 and Cp are heat capacities of
calorimeter and water respectively. Since, thermal conductivity of
glass is low, only that part of the beaker gains maximum heat which
comes in contact with water therefore, we can calculate only effective
m1 C p1 (i.e. calorimeter constant, W). On rewriting equation (3) we
get
W (tm– tc) + m2Cp (tm– tc) + m3Cp (tm– th) = 0
m 2 C p (t m – t c ) + m 3 C p (t m – t h )
W= ... (4)
(t m – t c )
but mCp = VdCp, where V, d and Cp are volume, density and

heat capacity of water respectively. By definition, heat capacity of
a substance is the amount of energy required to raise the
temperature of 1 g of substance by 1 K (or 1°C). The amount of
energy required to raise the temperature of 1 g of water by 1 K (or
1°C) is 4.184 Joules. This means that for 1 g water for rise of
–1
1 Kelven temperature VdCp = 4.184 JK . Therefore, product of
–1 –1
density and heat capacity can be taken as 4.184 J.mL .K . Thus,
equation (4) can be written as :
(4.184) [Vc (t m – t c ) + Vh (t m – t h ) –1
W= JK ... (5)
(t m – t c )
where Vc = volume of cold water
Vh = volume of hot water
Technique for measuring the enthalpy changes are given in
the following experiments.
EXPERIMENT 3.1
Aim
To determine the enthalpy of dissolution of copper sulphate/
potassium nitrate.
Theory
In thermochemical measurements generally aqueous solutions are
mixed therefore, water in the reaction medium and the temperature
changes result due to the chemical reactions taking place in
solution.
20
THERMOCHEMICAL MEASUREMENT
According to law of conservation of energy, the sum of enthalpy

changes taking place in the calorimeter (loss and gain of energy)
must be zero. Thus, we can write the following equation-
(∆H1) (∆H2) (∆H3) (∆H4)

Heat gained by Enthalpy Enthalpy change Enthalpy
calorimeter, + change of
+
of added solution/
+
change of
= 0 .. (6)
thermometer solution/water water in reaction
and stirrer in calorimeter calorimeter
In these reactions we take the product of density and heat

capacity of solutions, dCp, to be 4.184 J.mL–1.K–1, nearly the same
as that of pure water.*
Solution formation often accompanies heat changes. Enthalpy
of solution is the amount of heat liberated or absorbed when one
mole of a solute (solid/liquid) is dissolved in such a large quantity
of solvent (usually water) that further dilution does not make any
heat changes.
Material Required
• Beakers (250 mL) : Three

• Glass rod : One
• Copper sulphate/
• Cotton wool : As per need
potassium nitrate : 2g
• Small wooden block : One
• Small piece of cardboard : One
• Stirrer : One
Procedure
A. Determination of Calorimeter constant of calorimeter
(Beaker)
(i) Take 100 mL of water in a 250 mL beaker marked ‘A’.
(ii) Place this beaker on a wooden block kept in a larger beaker
of capacity 500 mL (Fig. 3.1).
(iii) Pack the empty space between the large and the small
beaker with cotton wool. Cover the beaker with a cardboard.
Insert thermometer and stirrer in the beaker through it.
* Density of the solutions is 4 to 6% higher than that of pure water and heat capacity is about 4 to 8% less than
pure water so the product of density and heat capacity (dCp ) is nearly the same as the product of pure water.
21
Fig. 3.1 : Determination of calorimeter constant
(iv) Record the temperature of water. Let this temperature

be tc°C.
(v) In another beaker of 250 mL capacity marked ‘B’ take
100 mL of hot water (50-60°C).
(vi) Note the exact temperature of hot water. Let this
temperature be th°C.
(vii) Lift the card board and pour the hot water contained in
beaker B into beaker A. Stir the mixed water and note the
temperature. Let this temperature be tm°C.
(viii) Calculate the calorimeter constant of the beaker by using
the expression (5) given above.
(Remember the three temperatures are in the order th > tm >tc).
B. Determination of Enthalpy of Dissolution
(i) Take 100 mL of distilled water in the beaker of which

calorimeter constant has been determined and place it on
a wooden block kept in a larger beaker of capacity 500
mL (Fig. 3.1).
(ii) Pack the empty space between the larger and the smaller
beaker with cotton wool and cover with a cardboard.
(iii) Record the temperature of water already taken in the small
beaker. Let this be t'1°C.
(iv) Add weighed amount, say W1 g of well powdered copper
sulphate in water and stir the solution with a stirrer till
the entire amount of copper sulphate dissolves.
22
(v) Note down the temperature attained by the solution after

the addition of copper sulphate. Let this be t'2°C. Calculate
the enthalpy of dissolution of copper sulphate as follows:
Total mass of the solution = Mass of Solvent + Mass of Solute
= (100 + W1) g
–1
(Assuming density of water to be equal to 1 gL at the
experimental temperature)
Note : To find out enthalpy
Change in temperature = (t'2 - t'1) °C
change for the dissolution
Enthalpy change of the calorimeter (beaker) = W (t'2 - t'1) of potassium nitrate, use
where, W = Calorimeter constant potassium nitrate in place
of copper sulphate in this
Enthalpy change of solution = [(100 + W1) (t'2 - t'1)] 4.184 J experiment.
for (t'2 - t'1) °C rise in temperature
Total enthalpy change

of the Calorimeter = [W (t'2 - t'1) + (100 + W1) (t'2 – t'1)] × 4.184 J
(beaker) and solution
Heat liberated
on dissolution [W (t'2 - t'1 ) + (100 + W1 ) (t'2 - t'1 )] × 4.184 J
=
of 1 g copper W1
sulphate
Since 1 mol of copper sulphate weighs 249.5 g. Therefore,
[W(t'2 – t'1 ) + (100 + W 1 )(t'2 – t'1 )] 4.184 –1

∆ Sol H of CuSO4 .5H 2O = 249.5 × J mol
W1
Result
Enthalpy change in the dissolution of copper sulphate/potassium
–1
nitrate is _______ Jmol .
Precautions
(a) To record the temperature of water, use a thermometer with 0.1°C graduation.
(b) In the determination of calorimeter constant record the temperature of hot water
just before mixing.
(c) Avoid using very large amounts of copper sulphate/potassium nitrate.
(d) Stir the solution well to dissolve the solid and record the temperature. Avoid too
much stirring, it may produce heat due to friction.
(e) Weigh copper sulphate carefully as it is hygroscopic in nature.
(f) Use cotton wool to create insulation between the two beakers.
23
(i) What is meant by the term, calorimeter constant?
(ii) Why is ∆Sol H for some substances negative while for others it is positive?
(iii) How does ∆Sol H vary with temperature?
(iv) Will the enthalpy change for dissolution of same amount of anhydrous copper sulphate and
hydrated copper sulphate in the same amount of water be the same or different? Explain.
(v) How will the solubility of copper sulphate and potassium nitrate be affected on increasing
the temperature? Explain.
EXPERIMENT 3.2
Aim
To determine the enthalpy of neutralisation of a strong acid (HCl)
with a strong base (NaOH).
Theory
+
A neutralisation reaction involves the combination of H (aq) ions
–
furnished by an acid and OH (aq) ions furnished by a base,
evidently leading to the formation of H2O (l). Since the reaction
envisages bond formation, therefore, this reaction is always
exothermic. Enthalpy of neutralisation is defined as the amount
+
of heat liberated when 1mol of H ions furnished by acid combine
–
with 1 mole of OH ions furnished by base to form water. Thus:
+ –
H (aq) + OH (aq) → H2O (l), ∆neut H is negative
(Acid) (Base)
where ∆neut H is known as enthalpy of neutralisation.

If both the acid and the base are strong then for the
formation of 1 mol H2O (l), always a fixed amount of heat, viz,
–1
57 kJ mol is liberated. If any one of the acid or the base is
weak or if both of these are weak, then some of the heat
liberated is used for the ionisation of the acid or base or both
of them (as the case may be) and the amount of heat liberated
–1
is less than 57 kJ mol .
24
Material Required
• Beakers (250 mL) : Three

• Glass rod : One
• Cotton wool : As per need • 1 M HCl : 100 mL
• Small wooden block : One • 1 M NaOH : 100 mL
• Piece of cardboard : One
• Stirrer : One
• Calorimeter : One
Procedure
A. Determination of calorimeter constant

This may be determined by following the procedure, as detailed in
experiment 3.1.
B. Determination of Enthalpy of Neutralisation
(i) Take 100 mL of 1.0 M HCl solution in the calorimeter (beaker)
and cover it with cardboard. In another beaker of 250 mL
capacity take 100 mL of 1.0 M NaOH solution.
(ii) Note down the temperature of both the solutions, which is
likely to be the same. Let it be t1°C.
(iii) Pour 100 mL 1 M NaOH solution into the calorimeter
containing 100 mL of 1.0 M HCl solution.
(v) Mix the solutions by stirring and note the final temperature
of the mixture. Let it be t2°C.
Calculate the enthalpy of neutralisation as follows:
(i) Note the rise in temperature of the mixture, which in this
case is (t2-t1) °C.
(ii) Calculate the total amount of heat produced during the
neutralisation process, using the following expression
Heat evolved = (100 + 100 + W) (t2 - t1) × 4.18 J
(where W, is the calorimeter constant)
(iii) Finally calculate the heat evolved when 1000 mL of 1M HCl
is allowed to neutralise 1000 mL of 1M NaOH. This quantity
would be ten times the quantity obtained in step (ii).
–1
(iv) Express the quantity of heat evolved in kJ mol .
Result
Enthalpy change in the neutralisation of hydrochloric acid solution
–1
with sodium hydroxide solution _______ kJmol .
25
Precautions
(a) Record the temperature carefully with the help of a thermometer graduated up to
0.1°C.
(b) Measure the volume of hydrochloric acid and sodium hydroxide solution to be
taken for the experiment carefully.
(c) Proper insulation should be made between the two beakers.
(d) Avoid unnecessary and excessive stirring to prevent heating due to friction.
(i) Why do we calculate the heat evolved for the neutralisation of 1000 mL of a (1 M) acid by
1000 mL of a (1 M) monoacidic base?
(ii) In comparison to heat evolved in neutralisation reaction between a strong acid and a strong
base. Why is lesser quantity of heat evolved when any one of the acid or the base is weak
and still less when both are weak?
+ –
(iii) Why does the reaction: H2O (l) H (aq) + OH (aq) proceed in the forward direction with rise
in temperature of the system?
EXPERIMENT 3.3
Aim
To determine the enthalpy change for the interaction between

acetone and chloroform (hydrogen bond formation).
Theory
On mixing, liquid pairs show departure from ideal behaviour.
Acetone and chloroform form non-ideal liquid pair system, which
shows a negative deviation from Raoult’s law. This negative deviation
from Raoult’s law implies that the two components are strongly held
together in liquid state on mixing due to hydrogen bonding. On the
other hand in the pure state, only weak Van der waal’s forces hold
molecules of chloroform as well as acetone. The hydrogen bonding
between the molecules of acetone and chloroform is depicted as
follows:
Hydrogen bonding between

chloroform and acetone
26
In this process enthalpy change takes place due to hydrogen

bond formation. The enthalpy change is an extensive
thermodynamic property, therefore, the heat evolved from the
system depends upon the amount of the liquid components
mixed. It is for this reason that the heat change is reported for
specified amount. Therefore, enthalpy change during mixing of
1 mol chloroform with 1 mol acetone is reported.
(∆H1) (∆H2) (∆H3) (∆H4)

Heat gained by Enthalpy Enthalpy Enthalpy
calorimeter, + change of + change for + change of = 0
thermometer chloroform acetone interaction
and stirrer
∴ ∆H4 = – (∆H1+∆H2+∆H3)
Material Required

• Boiling tube : One
• Thermometer (110°C): One
• Cotton wool : As per need
• Glass rod : One • Chloroform : 20 mL
• Measuring • Acetone : 10 mL
cylinder (250mL) : One

• Piece of cardboard : As per need
• Stirrer : One
Procedure
A. Determination of calorimeter constant Chloroform
This may be determined in a manner detailed in previous
experiments; except that here instead of a beaker, boiling tube
may be taken and 8 mL of cold and 7.5 mL of hot water can be Acetone
used instead of 100 mL.
27
B. Determination of Enthalpy Change on

Mixing Chloroform and Acetone*
(i) Transfer the volume of chloroform
equivalent to 0.1 mol (≈ 8.14 mL) after
measuring from a measuring cylinder
into the insulated boiling tube as shown
in Fig. 3.2. Let the mass of chloroform
taken be m1 grams.
(ii) Record the temperature of chloroform.
Let it be t1°C.
(iii) Transfer the volume of acetone equivalent
to 0.1 mol of acetone (≈ 7.34 mL) in a
clean measuring cylinder. Let its mass
be m2 grams.
(iv) Record the temperature of acetone. Let
it be t2°C.
(v) Pour acetone from the measuring
cylinder into the chloroform contained
in the insulated boiling tube.
(vi) Stir gently the mixture of chloroform
and acetone carefully with the help of
a stirrer.
Fig. 3.2 : Determination of enthalpy of interaction
of chloroform and acetone (vii) Record the temperature of the
mixture of chloroform and acetone.
Let it be t3°C.
Molar mass of CHCl 3

*Volume of one mole of CHCl3 = Density of CHCl 3
1
Volume of 0.1 mole = th of the above volume
10
(Similarly you can calculate the volume of 0.1 mole of acetone).
Density of chloroform= 1.47 g /mL Density of acetone = 0.79 g /mL
Molar mass of chloroform = 119.5 g Molar mass of acetone = 58.0
1.47 g = 1 mL volume 0.79 g = 1 mL
119.5 58
119.5 g = mL 58 g = mL
1.47 0.79
1 mole = 81.4 mL 1 mole = 73.4 mL
0.1 mole = 8.14 mL 0.1 mole = 7.34 mL
Total volume of acetone and chloroform = 8.14 +7.34 = 15.48 mL
28
Calculate the enthalpy of interaction as follows :
(i) Let the room temperature be t°C, then heat gained by

calorimeter (boiling tube) is W × (t3 – t), where W is the
calorimeter constant, i.e. boiling tube in this experiment.
(ii) Note the value of specific heat of chloroform from literature.
Let it be q1.
Then heat gained by chloroform = m1 × q1 × (t3 - t1).
(iii) Note the value of the specific heat for acetone from literature.
Let it be q2. Thus heat gained by acetone = m2 × q2 × (t3 - t2).
(iv) Total heat gained by all the three components, i.e. boiling
tube, chloroform and acetone = – {W×(t3 – t1) + m1×q1×(t3 – t1) +
m2 × q2 × (t3 – t 2)}. This in fact is the enthalpy change of
interaction, on mixing 0.1 mol chloroform with 0.1 mol acetone.
The negative sign simply implies that the mixing of
chloroform and acetone is an exothermic process.
Note : Here, care should be taken that the total volume of acetone and chloroform
is equal to the volume of water for which water equivalent of the
calorimeter has been calculated.
Precautions
(a) Measure chloroform and acetone carefully.

(b) Record the temperature very carefully with a thermometer graduated up to 0.1°C.
(i) Chloroform and acetone do not form an ideal liquid pair, whereas acetone and benzene do
form. Why?
(ii) Why does liquid pair of ethanol and water show positive deviation from Raoult’s law?
(iii) Give two examples of each of the liquid pairs for which ∆Mixing H is negative and positive
respectively.
(vi) How is the vapour pressure of the liquids related to interaction pattern between the
molecules of the components of a liquid mixture?
(v) How can you correlate the heat evolved from the system with the strength of the hydrogen
bond?
29
UNIT-6
(REDOX REACTIONS)
T
HE oxidation and reduction reactions in aqueous solutions involve the
transfer of electrons from one species to another. In the oxidation of a
substance electron(s) is (are) transfered from the species and in reduction,
electron(s) is (are) gained by the species. Oxidation and reduction reactions occur
simultaneously. A reaction, which involves simultaneous oxidation and
reduction, is called a redox reaction. The titrations involving redox reaction are
called redox titrations. You know that in acid-base titrations, indicators which
are sensitive to pH change are employed to note the end point. Similarly, in
redox titrations there is a change in oxidation potential of the system.
The indicators used in redox reactions are sensitive to change in oxidation
potential. The ideal oxidation-reduction indicators have an oxidation potential
intermediate between the values for the solution being titrated and the titrant
and these show sharp readily detectable colour change.
EXPERIMENT 6.1
Aim
To determine the concentration/molarity of KMnO4 solution by titrating it against
a 0.1 M standard solution of oxalic acid.
Theory
In the present experiment, potassium permanganate acts as a powerful
oxidising agent. Although KMnO4 acts as an oxidising agent in alkaline medium
also, for quantitative analysis mostly acidic medium is used. The oxidising
action of KMnO4 in the acidic medium can be represented by the following
equation:
– –
MnO4 + 8H+ +5e → Mn2+ + 4H2O
The acid used in this titration is dilute sulphuric acid. Nitric acid is not used
as it is itself an oxidising agent and hydrochloric acid is usually avoided because
it reacts with KMnO4 according to the equation given below to produce chlorine
and chlorine which is also an oxidising agent in the aqueous solution.
2KMnO4 + 16 HCl → 2KCl + 2 MnCl2 + 5Cl2 + 8 H2O
TITRIMETRIC ANALYSIS (REDOX REACTIONS)
Since, oxalic acid acts as a reducing agent, it can be titrated

against potassium permanganate in the acidic medium according
to the following equation:
Reactions of oxalic acid
A. Chemical equations
Reduction half reaction : 2KMnO4 + 3H2SO4 → K2SO4 + 2MnSO4 + 3H2O + 5 [O]

60°C
Oxidation half reaction : H2 C2 O4 + [O]  → 2CO2 + H2 O] × 5
________________________________________________________________________________
2KMnO4 + 3H2SO4 + 5H2C2O4 → K 2SO 4 + 2MnSO4 + 8H2O + 10 CO2
________________________________________________________________________________
B. Ionic equation
– – + 2+
Reduction half reaction : MnO4 + 5e + 8H → Mn + 4H2O] × 2
– –
Oxidation half reaction : C2O4 → 2CO2 + 2e ] × 5
_____________________________________________________________________
– 2– + 2+
2 MnO4 + 5C2O4 + 16H → 2Mn + 10CO2 + 8H2O
_____________________________________________________________________
– 2+ 2–
In these equations, MnO4 is reduced to Mn and C2O4 is
2–
oxidised to CO2. The oxidation number of carbon in C2O4 changes
from +3 to +4.
In these titrations, potassium permanganate acts as a self-
indicator. Initially colour of potassium permanganate is discharged
due to its reduction by oxalic acid. After complete consumption of
oxalate ions, the end point is indicated by the appearance of a
light pink colour produced by the addition of a little excess of
unreacted potassium permanganate. Further, during the titration
of oxalic acid against potassium permanganate, warming of oxalic
acid solution (50°–60°C) along with dilute H2SO4 is required.
This is essential because the reaction takes place at higher
temperature. During the titration, first manganous sulphate is
formed which acts as a catalyst for the reduction of KMnO4 by
oxalic acid. Therefore, in the beginning the reaction rate is slow
and as the reaction proceeds, the rate of the reaction increases.
41
Material Required
• Measuring flask (250 mL): One

• Burette stand : One
• Pipette : One • Oxalic acid : As per need
• Conical flask : One • Potassium permanganate
• Funnel : One solution : As per need
• Weighing bottle : One • 1.0 M Sulphuric acid : As per need
• Glazed tile(white) : One
• Burner : One
• Wire gauze : One
• Chemical balance : One
Procedure
A. Preparation of 0.1 M standard solution of oxalic acid
Prepare 0.1M oxalic acid solution as mentioned in experiment
Oxalic acid 2.1(Unit 2, Class XI, Laboratory Manual)
B. Titration of oxalic acid solution against potassium
Potassium
permanganate permanganate solution
(i) Rinse and fill a clean burette with potassium permanganate
Sulphuric acid solution. Remove the air bubble, if any, from the nozzle of the
burette by releasing some solution through it. The burette
used in the permanganate titration must have a glass stop
cock as rubber is attacked by permanganate ions.
(ii) Take 10 mL of 0.1 M oxalic acid solution in a conical flask
and add half of the test tube full ( ≈ 5 mL) of 1.0 M H2SO4
to it to prevent the formation of any precipitate of
manganese dioxide during the course of the titration.
(iii) Heat the oxalic acid solution upto 50°– 60°C before titrating
it with potassium permanganate solution taken in the
burette. To increase the visibility of the colour change, place
the conical flask containing the solution to be titrated over
a white glazed tile kept below the nozzle of the vertically
fitted burette.
(iv) Note the initial reading of the volume of permanganate
solution in the burette and add it in small volumes to the
hot oxalic acid solution while swirling the contents of the
flask gently. The violet colour of permanganate solution is
42
discharged on reaction with oxalic acid. The end point is

indicated by the appearance of permanent light pink colour
due to a slight excess of permanganate solution.
(v) Repeat the titration till three concordant readings are
obtained. Since the solution of KMnO4 is of dark colour,
the upper meniscus should be considered for noting the
burette readings.
(vi) Record the readings as shown in observation Table 6.1 and
calculate the strength of potassium permanganate solution
in mols/litre.
Table 6.1 : Titration of potassium permanganate solution

against standard oxalic acid solution
Burette readings Volume (V) of

Sl. No. Volume of Oxalic
acid in mL KMnO4 used
Initial (x) Final (y) V = (y–x) mL
Calculations
(i) The strength of the unknown solution in terms of molarity
may be determined by the following equation.
a1M1V1 = a 2 M2 V2 (6.1)
For oxalic acid vs potassium permanganate titration:
a1 = 2, (the number of electrons lost per formula unit of
oxalic acid in a balanced equation of half cell reaction)
a2 = 5, (the number of electrons gained per formula unit
of potassium permanganate in the balanced equation
of half cell reaction)
M1 and M2 are the molarities of oxalic acid and potassium
permanganate solutions used in the titration.
V1 and V2 are the volumes of oxalic acid and potassium
permanganate solutions.
43
On putting the value of a1 and a2 in equation 6.1 we get

Oxalic acid KMnO4
2M1V1 = 5M2V2
2 M1V1
M2 = (6.2)
5 V2
We can calculate the molarity of potassium permanganate
solution by using equation 6.2. Strength of the solution is given by
the following equation:
Strength = Molarity × Molar mass
Result
(i) Molarity of KMnO4 solution is _______.
(ii) Strength of KMnO4 solution is _______.
Precautions
(a) Always rinse the burette and the pipette with the solutions to be taken in them.
(b) Never rinse the conical flask with the experimental solutions.
(c) Remove the air gaps if any, from the burette.
(d) Never forget to remove the funnel from the burette before noting the initial reading
of the burette.
(e) No drop of the liquid should hang at the tip of the burette at the end point and
while noting reading.
(f) Always read the upper meniscus for recording the burette reading in the case of
all coloured solutions.
(g) Never use pipette and burette with a broken nozzle.
(h) Lower end of the pipette should always remain dipped in the liquid while sucking
the liquid.
(i) Do not blow out the last drop of the solution from the jet end of the pipette.
(j) The strength of the solution must be calculated up to the fourth decimal place.
(k) Do not forget to heat the mixture of oxalic acid and H2SO4 solutions between 50°–60° C
while titrating it against potassium permanganate.
(i) What specific name is given to the permanganate titrations?

(ii) Which indicator is used in the permanganate titration?
44
(iii) Why is a burette with pinch-cock regulator not used for the permanganate titration ?
(iv) Why do we heat oxalic acid solution containing sulphuric acid up to 50–60°C in the
permanganate titration?
EXPERIMENT 6.2
Aim
To determine the concentration/molarity of KMnO4 solution by
titrating it against standard solution of ferrous ammonium
sulphate.
Theory
Like oxalic acid, ferrous ammonium sulphate also acts as a
reducing agent in the titration against potassium permanganate.
The reaction which takes place is given below :
(a) Chemical equation

Reduction half reaction : 2 KMnO4 + 3H2SO4 → K2SO4 + 2 MnSO4 + 3H2O + 5 [O]
Oxidation half reaction : 2 FeSO4 (NH4)2 SO4 . 6H2O + H2SO4 + [O] → Fe2 (SO4) 3 + 2 (NH4)2 SO4
+ 13 H2O] x 5
_______________________________________________________________________________________
2KMnO4 + 8H2SO4 + 10FeSO4 (NH4)2 SO4 . 6H2O → K2SO4 + 2MnSO4 + 5Fe2(SO4)3
+ 10(NH4)2SO4 + 68H2O
_______________________________________________________________________________________
(b) Ionic equation

– – + 2+
Reduction half reaction : MnO4 + 5e + 8H → Mn + 4H2O
2+ 3+ –
Oxidation half reaction : Fe → Fe + e ] × 5
_______________________________________________________________________________________
MnO4– + 5Fe2+ + 8H+ → Mn2+ + 5Fe3+ + 4H2O
_______________________________________________________________________________________
The oxidation number of iron in Mohr’s salt is +2. Iron is

oxidised during the reaction and its oxidation number changes
from +2 to +3. In this titration heating of ferrous ammonium
sulphate solution is not required because reaction rate is very
high even at room temperature. Also, at high temperatures, ferrous
ions may be oxidised to ferric ions by oxygen of air and error may
be introduced in the experiment.
45
Material Required

• Burette (50 mL) : One • Potassium
• Burette stand : One permanganate solution : As per need
• Pipette : One • Dilute sulphuric acid : As per need
• Conical flask : One • Ferrous ammonium
• Glazed tile (white) : One sulphate : As per need
• Funnel : One
• Weighing bottle : One
Procedure
A. Preparation of 0.05 M, standard solution of ferrous
Potassium
permanganate
ammonium sulphate
–1
(Molar mass of FeSO4(NH4)2SO4 . 6H2O = 392 g mol ).
(i) Weigh 4.9000 g of ferrous ammonium sulphate and
Sulphuric acid
transfer it into a 250 mL measuring flask through a funnel.
(ii) Transfer the solid sticking to the funnel with the help of
distilled water into the flask and add dilute H 2 SO4 into the
flask drop wise to get the clear solution.
(iii) Shake the flask till the substance dissolves and make the
solution upto the mark.
B. Titration of ferrous ammonium sulphate against

potassium permanganate solution
(i) Rinse and fill the clean burette with potassium
permanganate solution. Remove air bubbles if any, from
the burette tip by releasing some solution through it.
(ii) Take 10 mL of 0.05 M ferrous ammonium sulphate solution
in a conical flask and add half test tube (≈ 5 mL) full of
(1.0 M) H2SO4 to it.
(iii) Titrate the above solution with potassium permanganate
solution till the colour of the solution changes to permanent
pink. Swirl the content of the flask during the titration.
(iv) Repeat the titration, until three concordant readings are
obtained.
(v) Record the readings as shown in observation Table 6.2 and
calculate the strength of potassium permanganate solution
in mols/litre.
46
Table 6.2 : Titration of potassium permanganate solution against

standard ferrous ammonium sulphate solution
Volume of ferrous Burette Readings Volume (V) of

ammonium sulphate
Sl. No. KMnO4 used
solution used for
Initial (x) Final (y) V = (y–x) mL
each titration in mL
Calculations
The strength of unknown solution in terms of molarity may be
determined by the following equation :
a1M1V1 = a2M2V2
M1 and M2 are the molarities of ferrous ammonium sulphate
and potassium permanganate solutions and V1 and V2 are volumes
of ferrous ammonium sulphate and potassium permanganate
solutions, respectively.
a1 = 1, (the number of electrons lost per formula unit of ferrous
ammonium sulphate in the half cell reaction)
a2 = 5, (the number of electrons gained per formula unit of
potassium permanganate in a half cell reaction)
Strength can be calculated by the formula given below :
Strength = Molarity × Molar mass
Result
The strength of the given potassium permanganate solution is _____ g/L.
Precautions
(a) Always use a fresh sample of ferrous ammonium sulphate to prepare its standard
solution.
(b) Other precautions are same as that in Experiment 6.1.
47
(i) Why is ferrous ammonium sulphate solution not heated before titration?
(ii) Why is nitric acid or hydrochloric acid not used in permanganate titration? Explain.
(iii) Why is dilute sulphuric acid added while preparing a standard solution of ferrous
ammonium sulphate ?
(iv) How will you prepare 100 mL of 0.1 M standard solution of ferrous ammonium sulphate?
(v) Why is KMnO4 not regarded as a primary standard?
(vi) What type of titrations are given the name redox titrations? Name some other redox
titrations?
48
UNIT-8
TESTS FOR FUNCTIONAL GROUPS
IN ORGANIC COMPOUNDS
EXPERIMENT 8.1
Aim
To identify the functional groups present in an organic compound.
I. TESTS FOR UNSATURATION
Theory
Organic compounds containing > C = C < and / or — C ≡ C – bonds are called
unsaturated compounds. These compounds undergo addition reaction with
bromine water or the solution of bromine in carbon tetrachloride, chloroform or
glacial acetic acid. Addition of bromine to an alkene results in the formation of
vicinal dibromide. The reddish orange colour of the solution of bromine in carbon
tetrachloride disappears on reaction with an alkene. The reaction is as follows :
Alkenes decolourise the neutral/alkaline KMnO4 solution and vicinal glycols

are formed (Bayer’s test). Reaction takes place as follows :
Both the above reactions are used as tests for unsaturation.

TESTS FOR FUNCTIONAL GROUPS IN ORGANIC COMPOUNDS
Material Required
• Potassium hydroxide
solution : 1–2 mL
• Carbon tetrachloride/
chloroform : 2 mL
• Test tubes : Two
• Bromine water/solution
• Test tube holder : One
of bromine in CCl4 or
chloroform : 2 mL
• Potassium permanganate
• Compound to be tested : As per need
Procedure
A. Bromine water test
Dissolve 0.1 g or 5 drops of organic compound in 2 mL of carbon Potassium
tetrachloride in a test tube and add 2% solution of bromine in hydroxide
carbon tetrachloride or bromine water drop by drop with
continuous shaking. Decolourization of bromine solution indicates
the presence of unsaturation in organic compound. Carbon
tetrachloride
B. Bayer’s test
Chloroform
Dissolve 25-30 mg of organic compound in 2 mL of water or
acetone (free of alcohol) and add 1% potassium permanganate
solution containing equal volume of 1% sodium carbonate Bromine
solution. The discharge of the colour of more than one drop of
potassium permanganate indicates the presence of unsaturation Potassium
in the organic compound. Carrying out the reaction under alkaline permanganate
conditions removes the possibility of confusion due to substitution

in aromatic compounds.
Note: (i) Unsaturation in an organic compound is confirmed only when

both of the above tests are positive.
(ii) In place of CCl4 any other solvent such as CHCl3/dioxan and
even water can be used to dissolve the organic compound for
carrying out the reaction.
Precautions
(a) The tests should be performed at room temperature.

(b) Handle bromine solution carefully. Do not inhale the vapours and also avoid its
contact with the skin.
87
II. TEST FOR ALCOHOLIC (R–OH) GROUP
Theory
Alcoholic compounds on reaction with ceric ammonium nitrate
give a red colouration due to the formation of a complex.
(NH4)2 [Ce(NO3)6] + 3ROH → [Ce(NO3)4(ROH)3] + 2NH4NO3
Ceric ammonium Red complex
nitrate
Distinction between primary, secondary and tertiary alcohols
can be done on the basis of iodoform test and Lucas test.
Ethanol and secondary alcohols which contain CH3—CH(OH)R
group (iodoform reaction) give positive iodoform test. To carry out
reaction, potassium iodide and sodium hypochlorite solution are
added to the compound in the presence of sodium hydroxide
solution. Probably sodium hypochlorite first oxidses potassium
iodide into potassium hypoiodite, which oxidises CH3—CH(OH)R
group to CH3COR group and then iodinates it in the alkaline
medium of the reaction mixture by replacing the α-hydrogen
attached to the carbon atom adjacent to carbonyl group by iodine.
Iodoform is formed after cleavage of C—C bond.
Potassium Potassium
hypoiodite hypoiodite
NaOH
CH3CH2OH → CH3CHO → CI3CHO  → CHI3 + HCOONa
Lucas Test
Lucas reagent contains zinc chloride and concentrated
hydrochloric acid. This reagent reacts with primary, secondary
and tertiary alcohols at different rates. Tertiary alcohols react
almost instantaneously, secondary alcohols react in about 1-5
minutes and primary alcohols react very slowly. The reaction may
take 10 minutes to several days.
ZnCl
2
RCH2OH+HCl → No reaction/Slow reaction
ZnCl
2
R 2CHOH+HCl → R 2CHCl+H2O
ZnCl
2
R 3COH+HCl → R 3CCl+H2O
Alcohols are soluble in Lucas reagent but the formed alkyl
halides are not soluble. Therefore, formation of two layers in the
reaction medium indicate the occurrence of the reaction.
Primary alcohols – Layers do not separate
Secondary alcohols – Layers separate within 1-5 minutes
Tertiary alcohols – Layers separate immediately
88
Material Required
• Ceric ammonium
nitrate solution : As per need
• Test tube holder : One • Sodium hydroxide : As per need
• Test tubes : As per need • Iodine solution : As per need
• Lucas reagent : As per need
• Dioxan : As per need
Procedure
A. Ceric ammonium nitrate test
Take 1 mL solution of organic compound dissolved in a suitable Sodium
solvent. Add a few drops of ceric ammonium nitrate solution. hydroxide
Appearance of red colour shows the presence of alcoholic – OH group.

Iodine
Note : The red colour disappears after keeping the reaction mixture for
sometime. The colour also disappears if excess of ceric
ammonium nitrate solution is added. Therefore, use of excess
of ceric ammonium nitrate solution should be avoided.
B. Iodoform test
First method
Take 0.2 mL of the compound in a test tube, add 10 mL of 10%
aqueous KI solution and 10 mL of freshly prepared NaOCl solution.
Warm gently; yellow crystals of iodoform separate.
Second method
Dissolve 0.1 g or 4 to 5 drops of compound in 2 mL of water. If it
does not dissolve, add dioxane drop by drop to get a homogeneous
solution. Add 2 mL of 5% sodium hydroxide solution followed by
potassium iodide-iodine reagent* dropwise with continuous
shaking till a definite dark colour of iodine persists. Allow the
reactants to remain at room temperature for 2-3 minutes. If no
iodoform separates, warm the reaction mixture in a water bath at
60°C. Add more drops of potassium iodide–iodine reagent. If colour
of iodine disappears continue addition of reagent till the colour of
iodine persists even after two minutes of heating at 60°C. Remove
excess iodine by adding a few drops of sodium hydroxide solution
with shaking. Dilute the mixture with equal volume of water and
keep it at room temperature for 10-15 minutes. A yellow precipitate
of iodoform is obtained if test is positive.
* Potassium iodide-iodine reagent is prepared by dissolving 20 g of potassium

iodide and 10 g of iodine in 100 mL of water.
89
C. Lucas test
Take 1 mL of compound in a test tube. Add 10 mL of Lucas reagent.
Shake well and note the time for the separation of two distinct layers.
Note : Lucas test is applicable to only those alcohols which are soluble
in the reagent because the test is based on separation of alkyl
halides as separate layer.
III. PHENOLIC (AR-OH) GROUP
Theory
The –OH group attached directly to the ring carbon of an aromatic
ring is called phenolic –OH group. Phenols are weakly acidic,
therefore they are soluble in NaOH solution but at the same time
they are not sufficiently acidic to be soluble is sodium
hydrogencarbonate solution. Phenols give coloured complex with
neutral ferric chloride solution. For example, phenol gives a
complex of violet colour as follows :
3– +
6C6H5OH + FeCl3 → [Fe(C6H5O)6] + 3HCl + 3H
Violet complex
Resorcinol, o–, m– and p–cresol give violet or blue colouration,
catechol gives green colour which rapidly darkens. 1 and 2–Naphthol
do not give characteristics colours. Phenols condense with phthalic
anhydride in the presence of concentrated H2SO4, Phenol condeses to
give phenolphthalein which gives a dark pink colour with NaOH
solution. This is called phthalein dye test.
90
Table 8.1 : Colours produced by some other phenolic compounds in phthalein dye test
Compound Colour Compound Colour
o–Cresol red Catechol Usually blue takes

longer time to appear
m–Cresol bluish-purple
Resorcinol Green fluorescent
p–Cresol No colour
colour of fluorescein
Material Required
• Blue litmus paper

• Ferric chloride solution
• Conc. sulphuric acid
According
• Sodium hydroxide
• Test tube holder : One to
• Phthalic anhydride
• Test tubes : As per need requirement
• Organic compound
containing phenolic
–OH group
Procedure
A. Ferric chloride test
Sulphuric
Take 2 mL of aqueous or alcoholic solution of the organic acid
compound in a test tube, add neutral ferric chloride solution
dropwise and note the colour change. Appearance of a blue, green, Sodium
hydroxide
violet or red colour indicates the presence of phenolic –OH group.
B. Phthalein dye test Phthalic

anhydride
Take 0.1 g of organic compound and 0.1 g of phthalic anhydride
in a clean dry test tube and add 1-2 drops of conc. H2SO4. Heat
the test tube for about 1 minute in an oil bath. Cool and pour the
reaction mixture carefully into a beaker containing 15 mL of dilute
sodium hydroxide solution. Appearance of pink, blue, green, red
etc. colours indicates the presence of phenolic –OH group in the
compound. However, the colour disappears on addition of large
excess of sodium hydroxide solution.
Note : (i) Neutral ferric chloride solution is prepared by adding dilute sodium hydroxide solution to
ferric chloride solution drop by drop till a small but permanent brown precipitate appears.
Solution is filtered and the clear filtrate is used for the test.
(ii) Some phenols like 2,4,6 – trinitrophenol and 2,4 – dinitrophenol, which contain electron
withdrawing groups are strong acids and dissolve even in sodium hydrogencarbonate solution.
91
Precautions
(a) Always use freshly prepared, neutral and very dilute solution of ferric chloride.
(b) Phenol is toxic and corrosive in nature and should be handled with care.
O
IV. ALDEHYDIC AND KETONIC GROUPS (–CHO and –C–)
Theory
Both aldehydes and ketones contain carbonyl group (>C = O) and
are commonly known as carbonyl compounds. Identification of
aldehydes and ketones is done by two important reactions of
carbonyl group i.e.
(i) addition reaction on double bond of >C = O group and
(ii) oxidation of carbonyl group.
Addition reactions of derivatives of ammonia are important from
the point of view of identification of carbonyl compounds. Addition
is generally followed by elimination resulting in the formation of
unsaturated compound.
(R = alkyl, aryl or C6H5NH etc.)

These reactions are catalysed by an acid or a base and do not
occur under strongly acidic or basic conditions. Each reaction
requires an optimum pH for its occurrence. Therefore, maintenance
of pH is very important while carrying out these reactions.
As far as oxidation is concerned, aldehydes are easily oxidised
to carboxylic acids while ketones require relatively stronger
oxidising agents. Distinction can be made between these two types
of carbonyl compounds on the basis of difference in their reactivity.
Following tests are performed for the identification of aldehydic
and ketonic groups:
(i) On reaction with 2,4-dinitrophenylhydrazine (2,4-DNP), they
form the respective 2,4–dinitrophenyl hydrazones.
2, 4-Dinitrophenylhydrazine 2, 4 – Dinitrophenyl hydrazone of

carbonyl compound
92
These two carbonyl compounds (aldehydes and ketones) are

distinguished on the basis of tests using mild oxidising reagents,
like Tollen’s reagent and Fehling’s reagent or Benedict’s reagent.
Tollen’s reagent is an alkaline solution of silver cation complexed
with ammonia, and Fehling’s and Benedict’s reagents are alkaline
solutions containing cupric ions complexed with tartarate and
citrate ions respectively. Fehling’s reagent is freshly prepared by
mixing equal amounts of Fehling’s solution A and Fehling’s
solution B. Fehlings reagent deteriorates on keeping while Fehling’s
solutions A and B are quite stable. Fehling’s solution A is an
aqueous copper sulphate solution while Fehling’s solution B is
an alkaline solution of sodium potassium tartarate (Rochelle’s salt).
The reagent contains Cu2+ ion complexed with tartarate ions. The
structure of the complex is given below :
Copper tartarate complex

Benedict modified the original Fehling’s test by using a single
solution which is more convenient for the test. Benedict’s solution
is more stable than Fehling’s reagent and can be stored for a long
time. It is an alkaline solution containing a mixture of copper
sulphate and sodium citrate (2Na3C6H5O7.11H2O).
Complex formation decreases the cupric ion concentration
below that necessary for precipitation of cupric hydroxide. These
two reagents oxidize aldehydes while ketones remain unaffected.
The chemistry of these tests is as follows:
+ –
RCHO + 2[Ag (NH3)2] + 2OH → 2Ag + 3NH3 + H2O + RCOONH4
From Tollen’s reagent
2+ – –
RCHO + 2Cu (complexed) + 5OH → RCOO + Cu2O + 3H2O
Fehling’s solution
However, aromatic aldehydes do not give positive Fehling’s test.
2+ +
In Benedict test also, Cu ions are reduced to Cu ions in the
same manner as in the case of Fehling’s reagent.
Aldehydes also give pink colour with Schiff’s reagent (the
reagent is prepared by decolourising aqueous solution of
p–rosaniline hydrochloride dye by adding sodium sulphite or by
passing SO2 gas). Ketones do not respond to this test.
93
Material Required
• Schiff’s reagent : As per need
• Fehling’s solutions A and B: As per need
• Beaker (250 mL) : One • Silver nitrate : As per need
• Test tube holder : One • Dilute ammonium
• Test tubes : As per need hydroxide solution : As per need
• 2,4-Dinitrophenyl-
hydrazine reagent : As per need
Procedure
Silver nitrate
A. Test given by both aldehydes and ketones
Ammonia
solution 2,4-Dinitrophenylhydrazine test (2,4-DNP test)
Take 2-3 drops of the liquid compound in a test tube or in case of

Ammonia gas solid compound, dissolve a few crystals of it in 2-3 mL
alcohol. Add a few drops of an alcoholic solution of
2,4-dinitrophenylhydrazine. Appearance of yellow, orange or
orange-red precipitate confirms the presence of carbonyl group.
If precipitate does not appear at room temperature, warm the
mixture in a water bath for a few minutes and cool.
B. Tests given by aldehydes only
Following tests namely Schiff’s test, Fehling’s test and Tollen’s test
are given by aldehydes only.
Schiff’s test
Take 3-4 drops of the liquid compound or dissolve a few crystals

of organic compound in alcohol and add 2-3 drops of the Schiff’s
reagent. Appearance of pink colour indicates the presence of an
aldehyde.
Fehling’s test
Take nearly 1 mL of Fehling’s solution A and 1 mL of Fehling’s

solution B in a clean dry test tube. To this add 2-3 drops of the
liquid compound or about 2 mL of the solution of the solid
compound in water or alcohol. Heat the content of the test tube
for about 2 minutes in a water bath. Formation of brick red
precipitate of copper (I) oxide indicates the presence of an aldehyde.
This test is not given by aromatic aldehydes.
94
Benedicts test
Add 5 drops of the liquid compound or the solution of the solid

organic compound in water or alcohol to 2 mL Benedict’s reagent.
Place the test tube in boiling water bath for 5 minutes. An orange-
red precipitate indicates the presence of an aldehyde.
Tollen’s test
(i) Take 1 mL of freshly prepared (~ 2 %) silver nitrate solution

in a test tube. Add 1-2 drops of sodium hydroxide solution
to it and shake, a dark brown precipitate of silver oxide
appears. Dissolve the precipitate by adding ammonium
hydroxide solution drop-wise.
(ii) To the above solution, add an aqueous or an alcoholic
solution of the organic compound.
(iii) Heat the reaction mixture of step (ii) in a water bath for about
5 minutes. Formation of a layer of silver metal on the inner
surface of the test tube which shines like a mirror, indicates
the presence of an aldehyde.
Precautions
(a) Always use freshly prepared reagents to perform the tests.

(b) Do not heat the reaction mixture directly on a flame.
(c) After performing the test, destroy the silver mirror by adding dilute nitric acid
and drain off the solution with excess of water.
V. CARBOXYL GROUP (—COOH)
Theory
Organic compounds containing carboxyl functional groups are
called carboxylic acids.
The term carboxyl, derives its name from the combination of
words carbonyl and hydroxyl because carboxylic functional group
O
contains both of these groups ( —C—OH ). These acids turn blue
litmus red and react with sodium hydrogencarbonate solution to
produce effervescence due to the formation of carbon dioxide.
This is a test that distinguishes carboxylic acids from phenols.
RCOOH + NaHCO3 → RCOONa + H2O + CO2
95
These react with alcohols in the acidic medium to produce esters.
Conc.H SO
RCOOH 2 4 → RCOOR' + H O
+ R'OH 
∆ 2
Carboxylic Alcohol Ester

acid
Material Required
• Blue litmus paper

• Test tube holder : One /solution : As per need
• Glass rod : One • Ethyl alcohol : As per need
• Test tubes : As per need • Sodium hydrogencarbonate
Procedure
A. Litmus test
Ethyl alcohol Put a drop of the liquid compound or a drop of the solution of the
compound with the help of a glass rod on a moist blue litmus paper.
If the blue colour of the litmus paper changes to red, the presence of
either a carboxylic group or a phenolic group is indicated.
B. Sodium hydrogencarbonate test

Take 2 mL of saturated aqueous solution of sodium
hydrogencarbonate in a clean test tube. Add a few drops of the
liquid compound or a few crystals of solid compound to it.
The evolution of brisk effervescence of CO2 indicates the presence
of carboxyl group.
C. Ester test
Take about 0.1 g compound in a test tube, add 1 mL ethanol or
methanol and 2-3 drops of concentrated sulphuric acid. Heat the
reaction mixture for 10-15 minutes in a hot water bath at about
50°C. Pour the reaction mixture in a beaker containing aqueous
sodium carbonate solution to neutralise excess sulphuric acid
and excess carboxylic acid. Sweet smell of the substance formed
indicates the presence of carboxyl function in the compound.
Precaution
Add the compound in sodium hydrogencarbonate solution slowly so that

effervescence is visible clearly.
96
VI. AMINO GROUP (—NH2)
Theory
Organic compounds containing amino group are basic in nature.
Thus they easily react with acids to form salts, which are soluble
in water.
Both, aliphatic and aromatic amines are classified into three
classes namely– primary(–NH2), secondary(-NH-) and tertiary (-N<),
depending upon the number of hydrogen atoms attached to the
nitrogen atom. Primary amine has two hydrogen atoms, secondary
has one while tertiary amine has no hydrogen atom attached to
nitrogen.
(i) Carbylamine test
Aliphatic as well as aromatic primary amines give carbylamine test
in which an amine is heated with chloroform.
∆→
R-NH2 + CHCl3 + 3KOH  RNC + 3KCl + 3H2O
(R=alkyl or aryl group) (Carbylamine)
Caution!
Carbylamine so formed is highly toxic and should be destroyed
immediately after the test. For this cool the test tube and add
carefully an excess of conc. HCl.
(ii) Azo dye test

Aromatic primary amines can be confirmed by azo dye test. Primary
amine e.g. aniline reacts with nitrous acid generated in situ by the
reaction of sodium nitrite with HCl at 0–5°C to produce diazonium
salt. This couples with β-naphthol to give a scarlet red dye, which
is sparingly soluble in water.
97
Material Required
• Chloroform
• Potassium hydroxide
• Sodium nitrite solution
• Test tubes : As per need
• Aniline
• Test tube holder : One As per need
• β-Naphthol
• Bunsen burner : One
• Dilute hydrochloric acid
• Sodium hydroxide solution
• Ice
Procedure
A. Solubility test
Chloroform
Take 1 mL of given organic compound in a test tube and add a few
Aniline
drops of dilute HCl to it. Shake the contents of the test tube well. If
the organic compound dissolves, it shows the presence of an amine.
+
–
Potassium C6H5NH2 + HCl → C6H5NH3 Cl
hydroxide (Anilinium chloride
soluble in water)
Sodium nitrite B. Carbylamine test
Take 2-3 drops of the compound in a test tube and add 2-3 drops of
β-naphthol chloroform followed by addition of an equal volume of 0.5 M alcoholic
potassium hydroxide solution. Heat the contents gently. An obnoxious
smell of carbylamine confirms the presence of primary amino group
in the compound.
Caution!
Do not inhale the vapours. Destroy the product immediately by
adding concentrated hydrochloric acid and flush it into the sink.
C. Azo dye test
(i) Dissolve nearly 0.2 g of the compound in 2 mL of dilute
hydrochloric acid in a test tube. Cool the content of the test
tube in ice.
(ii) To the ice cooled solution add 2 mL of 2.5% cold aqueous
sodium nitrite solution.
(iii) In another test tube, dissolve 0.2 g of β-naphthol in dilute
sodium hydroxide solution.
(iv) Add diazonium chloride solution prepared in step (ii) into
the cold β-naphthol solution slowly with shaking.
The formation of a scarlet red dye confirms the presence of
aromatic primary amine.
98
Precautions
(a) Do not expose yourself to the vapours while performing carbylamine test because
isocyanide is highly poisonous. Destroy it immediately as described above.
(b) Maintain the temperature of the reaction mixture below 5°C during diazotisation,
as diazonium chloride is unstable at higher temperatures.
(c) Always add diazonium chloride solution into the alkaline solution of β-naphthol
and not vice-versa.
(i) What is Bayer’s reagent?

(ii) Why do alkenes and alkynes decolourize bromine water and alkaline KMnO4?
(iii) Explain why for the confirmation of unsaturation in a compound both the tests namely
test with bromine water and test with Bayer’s reagent should be performed.
(iv) Why does phenol decolourize bromine water?
(v) How will you distinguish between phenol and benzoic acid?
(vi) Why does benzene not decolourise bromine water although it is highly unsaturated?
(vii) Why does formic acid give a positive test with Tollen’s reagent?
(viii) Outline the principle of testing glucose in a sample of urine in a pathological laboratory?
(ix) Why is Benedict’s reagent more stable than Fehling’s reagent?
(x) How would you distinguish an aldehyde from a ketone by chemical tests?
(xi) How would you separate a mixture of phenol and benzoic acid in the laboratory by using
chemical method of separation?
(xii) Write the chemistry of diazotisation and coupling reactions.
(xiii) How can you distinguish between hexylamine (C6H13NH2) and aniline (C6H5NH2)?
(xiv) How can you distinguish between ethylamine and diethylamine?
(xv) How can CH3OH and C2H5OH be distinguished chemically?
(xvi) Why is solution of iodine prepared in potassium iodide and not in water?
(xvii) What is haloform reaction? What type of compounds generally give this reaction?
(xviii) How can you distinguish the compounds and by simple

chemical test?
99
UNIT-9
PREPARATION OF
INORGANIC COMPOUNDS
EXPERIMENT 9.1
Aim
To prepare double salts: ferrous ammonium sulphate (Mohr’s salt) and potash
alum.
Theory
When a mixture containing equimolar proportions of potassium sulphate and
aluminium sulphate or ferrous sulphate and ammonium sulphate is crystallised
from its solution, a double salt is formed. The formation of double salt may be
shown as follows:
K2SO4 + Al2 (SO4)3 + 24H2O → K2SO4 . Al2 (SO4)3 . 24H2O or 2KAl(SO4)2.12H2O
(Potash alum)
FeSO4 + (NH4)2 SO4 + 6H2O → FeSO4 . (NH4)2 SO4 . 6H2O
Ferrous ammonium sulphate (Mohr’s salt)
2+ 3+
Fe and Al ions undergo hydrolysis, therefore, while preparing aqueous
solutions of ferrous sulphate and aluminium sulphate in water, 2-3 mL dilute
sulphuric acid is added to prevent the hydrolysis of these salts.
Material Required

• Conical flask (50 mL) : One • Potassium sulphate : As per need
• Trough : One • Aluminium sulphate : As per need
• Glass rod : One • Ferrous sulphate : As per need
• Tripod stand : One • Ammonium sulphate : As per need
• Funnel : One • Dilute sulphuric acid : As per need
• Ethanol : As per need
• Wire gauze : One
Procedure
(a) Preparation of Double Salt: Potassium Aluminium Sulphate (Potash Alum)
(i) Take 10 mL of distilled water in a 50 mL beaker and heat it to about 40°C.
Dissolve 6.6 g of aluminium sulphate in it and add about 0.4 mL of dilute
sulphuric acid.
PREPARATION OF INORGANIC COMPOUNDS
(ii) Weigh 2.4 g of powdered potassium sulphate and transfer

it to the above solution.
(iii) Heat the solution with constant stirring till potassium
sulphate dissolves completely.
(iv) Allow the solution to cool to room temperature slowly.
(v) On cooling, white crystals of potash alum separate out. Ethanol
(vi) Decant the mother liquor and wash the crystals by gently
shaking with 1:1 cold water and alcohol mixture.
Sulphuric acid
(vii) Filter the crystals, dry these between the folds of a filter paper
and note the yield.
(b) Preparation of Double Salt: Ferrous Ammonium Sulphate
(i) Dissolve 3.5 g of ferrous sulphate and 1.7 g of ammonium
sulphate (weighed separately), in 5 mL of distilled water
contained in a 50 mL conical flask by heating. Add about
0.5 mL of dilute sulphuric acid to the flask and concentrate
the solution by heating till the crystallization point is reached.
(ii) Allow the mixture to cool to room temperature slowly.
(iii) On cooling, light green crystals of ferrous ammonium
sulphate separate out.
(iv) Decant the mother liquor and wash the crystals by shaking
with very small amounts of 1:1 cold water and alcohol
mixture to remove sticking mother liquor.
(iv) Separate the crystals by filtration wash with alcohol, dry
between the folds of a filter paper and record the yield.
Result
Yield of potash alum/Mohr’s salt is __________g.
Precautions
(a) Cool the solution slowly to get good crystals. Avoid rapid cooling.
(b) Do not disturb the solution while cooling.
(c) Avoid prolonged heating while preparing crystals of ferrous ammonium sulphate,
as it may oxidise ferrous ions to ferric ions and change the stoichiometry of the
crystals.
(i) Why do we take equimolar quantities of reacting compounds in the preparation of double salts?
(ii) In the preparation of ferrous ammonium sulphate, can concentrated sulphuric acid be
used in place of dilute sulphuric acid? Explain.
(iii) What is the difference between iron compounds; K4[Fe(CN)6] and FeSO4.(NH4)2SO4.6H2O?
101
(iv) What is the action of heat on potash alum?

(v) Why does an aqueous solution of potash alum turn blue litmus red?
(vi) What are the isomorphous substances?
3+
(vii) Give the name of some of the alums where cations are other than Al .
(viii) What is the difference between a complex compound and a double salt?
EXPERIMENT 9.2
Aim
To prepare potassium trioxalatoferrate(III).
Theory
When hydrated ferric chloride is dissolved in aqeous solution of
oxalic acid containing potassium hydroxide, green crystals of
potassium trioxalatoferrate(III) are obtained. The reaction involved
in the formation of these green crystals is as follows:
FeCl3 + 6KOH + 3 H2C2O4 → K3 [Fe (C2O4)3] + 3KCl + 6H2O
Material Required

• Ferric chloride : 2.5 g
• Porcelain dish : One
• Potassium hydroxide : 3.8 g
• Water bath : One
• Oxalic acid : 3.0 g
• Glass rod : One
• Ethanol : As per need
• Funnel : One
Procedure
(i) Prepare a solution of 3.0 g of oxalic acid in 12.5 mL of hot
Potassium
hydroxide water contained in a clean 50 mL beaker.
(ii) To the above solution, add 3.8 g of potassium hydroxide
Ethanol gradually in lots, with stirring so that it dissolves completely.
(iii) Add 2.5 g of ferric chloride into the above solution with
constant stirring till it is completely dissolved.
Oxalic acid
(iv) Filter the solution and concentrate the green filtrate by
heating in a porcelain dish over a water bath and cool the
mixture slowly.
(v) Filter the crystals so formed, wash with 1:1 mixture of cold
water and alcohol and dry them by pressing between the
folds of a filter paper.
102
PREPARATION OF INORGANIC COMPOUNDS
Result
Yield of potassium trioxalatoferrate (III) is _________ g.
Precautions
(a) Do not evaporate the entire solvent when the solution is being concentrated.
(b) Weigh the desired quantities of different substances accurately.
(c) Maintain the temperature of hot water around 40°C.
(d) Add potassium hydroxide to oxalic acid solution in small lots.
(i) Give IUPAC name of the compound called potassium ferrioxalate.

(ii) What is the coordination number of iron in potassium trioxalatoferrate(III)?
(iii) Give two examples of bidentate ligands other than oxalate ion.
(iv) Why does the compound, potassium trioxalatoferrate(III), not give tests for ferric ions?
(v) What are chelates ?
103
UNIT-10
PREPARATION OF
ORGANIC COMPOUNDS
EXPERIMENT 10.1
Aim
To prepare acetanilide.
Theory
The replacement of one hydrogen atom of the — NH2 group of aniline by CH3CO–
group in the presence of glacial acetic acid. Gives acetanilide. In the laboratory,
acetylation is usually carried out with acetic anhydride. Acetyl chloride may
also be used for the purpose of acetylation if acetic anhydride is not available.
Acetylation with CH3COCl is usually carried out in the presence of pyridine.
Material Required
• Funnel : One
• Round bottomed flask (100 mL) : One
• Beaker (250 mL) : One • Aniline : 5 mL
• Air condenser : One • Acetic anhydride
• Sand bath : One /Acetyl chloride : 5 mL
• Clamp and iron stand : One • Acetic acid / Pyridine : 5 mL
• Pumice stone : As per need
• Melting point assembly : One
Procedure
(i) Take 5 mL of aniline in a 100 mL round bottom flask and add acetylating
mixture containing 5 mL acetic anhydride and 5 mL glacial acetic acid.
Alternatively, you can use 5 mL of acetyl chloride and 5 mL of dry pyridine
as the acctylating mixture.
PREPARATION OF ORGANIC COMPOUNDS
(ii) Fit an air condenser on the mouth of the round bottom flask
after adding a few pumice stones and reflux the mixture Aniline
gently for 10-15 minutes on a sand bath.
(iii) Cool the reaction mixture and pour it slowly in 150-200 mL Acetic
anhydride
of ice cold water with stirring.
(iv) Filter the solid, wash it with cold water and recrystallise a Acetyl
small amount of sample from hot water containing a few chloride
drops of methanol or ethanol.
Acetic acid
(v) Report the yield and the melting point of the compound. causes
serious burn
Result
Pyridine
(a) Yield of acetanilide _______ g.
(b) Melting point of acetanilide is _______ °C.
Precautions
(a) Handle acetic anhydride and acetyl chloride carefully as they cause irritation to
the eyes and acetyl chloride also strongly fumes in air.
(b) Store acetylchloride under dry conditions.
(c) Handle pyridine with extreme caution. Dispense it in an efficient fume cupboard
and wear disposable glasses while using it.
(d) Distil pyridine before use because it absorbs mioisture and the reaction does not
take place under moist conditions.
(e) Wash the solid 2-3 times with cold water till the filtrate is neutral to litmus.
(f) Determine the melting point of perfectly dried and recrystallised sample.
ALTERNATIVE METHOD FOR THE PREPARATION OF ACETANILIDE
If acetic anhydride or pyridine is not available then the following

method can be used for the preparation of acetanilide.
Material Required
• Boiling tube : One

• Aniline : 1 mL
• Water bath : One
• Glacial acetic acid : 1 mL
• Acetyl chloride : 1 mL
• Funnel : One
105
Procedure
(i) Take 1 mL of aniline in a dry boiling tube, add 1 mL of glacial
acetic acid to it and mix the two thoroughly.
(ii) To the above mixture add 1 mL of acetyl chloride in lots
(0.3 mL at a time). The mixture becomes warm. If the boiling
tube becomes unbearable to touch, cool it under tap water.
(iii) After addition of whole amount of acetyl chloride, heat the
mixture for five minutes in a boiling water bath.
(iv) Cool the boiling tube and add ice-cold water (~10 mL) into
the tube with constant stirring.
(v) Filter the acetanilide separated as white powder and wash
with water till filtrate is neutral to litmus.
(vi) Crystallise the crude acetanilide with hot water. White shining
needle shaped crystals are obtained.
(vii) Report the yield and melting point of the compound.
Precautions
(a) If aniline sample is too much coloured, distill it before carrying out the experiment,
because yield is lowered with impure aniline.
(b) Use perfectly dry apparatus.
(c) Do not inhale the vapours coming out during the addition of acetylchloride.
(d) Determine the melting point of perfectly dried and recrystallized sample.
EXPERIMENT 10.2
Aim
To prepare dibenzalacetone (Dibenzylideneacetone)
Theory
α-Hydrogen atom of aliphatic aldehydes and ketones is acidic in
nature, therefore, in the presence of dilute alkali, such an aldehyde
or ketone condenses with an aromatic aldehyde to give α, β–
unsaturated aldehyde or ketone. This reaction is called Claisen -
Schmidt reaction. For example, benzaldehyde undergoes
condensation with acetone in the presence of aqueous sodium
hydroxide (NaOH) to give dibenzalacetone.
106
Material Required
• Ethanol : 25 mL
• Conical flask(250 mL) : One • NaOH : 3.15 g
• Beaker(250 mL) : One • Benzaldehyde : 3.2 mL
• Funnel : One • Acetone : 2.3 mL
• Melting point assembly : One • Ice : As per need
• Ethylacetate : As per need
Procedure
(i) Prepare a solution of 3.15 g sodium hydroxide in a mixture Ethanol
of 25 mL ethanol and 30 mL distilled water taken in a 250 mL
beaker. Cool the beaker in an ice bath maintained at a
NaOH
temperature of about 20–25°C.
(ii) Prepare a mixture of 3.2 mL of benzaldehyde and 2.3 mL of
acetone and add half of this mixture slowly in ice cooled Benzaldehyde
NaOH solution prepared in step (i) with vigourous stirring.
A fluffy precipitate is formed within 1-2 minutes. Stir the Acetone
mixture gently for about fifteen minutes.
(iii) After 15 minutes add remaining mixture of benzaldehyde
Ethyl acetate
and acetone and stir for 30 minutes more.
(iv) Filter the pale yellow solid so obtained and wash with cold
water. Dry it and recrystallise its small amount from ethanol
or ethyl acetate.
(v) Report the yield and the melting point of the compound.
Result
(a) Yield of dibenzalacetone is _________g.
(b) Melting point of dibenzalacetone _______°C.
Precautions
(a) Maintain the temperature around 20°C while shaking the reaction mixture.
(b) Always use freshly distilled benzaldehyde or the sample from a freshly opened
bottle.
EXPERIMENT 10.3
Aim
To prepare p-nitroacetanilide.
107
Theory
p-Nitroacetanilide is prepared by the nitration of acetanilide by
using a mixture of conc. nitric acid and conc. sulphuric acid as
nitrating reagent. The mixture of the two acids releases nitronium
+
ion( NO2 ), which acts as an electrophile in the reaction.
+ + –
HNO3 + 2H2SO4 → NO2 + H3O + 2HSO 4
Nitronium ion attacks the benzene ring containing anilide
group, mainly at the para position to give p-nitroacetanilide as a
major product. This is an example of aromatic electrophilic
substitution reaction.
Material Required
• Acetanilide : 2g
• Beaker (100 mL) : One • Glacial acetic acid : 2 mL
• Funnel : One • Conc. H2SO4 : 5 mL
• Glass rod : One • Conc. HNO3 : 1.5 mL
• Ice bath : One • Ice : As per requirement
• Ethanol/methanol : As per requirement
Procedure
Acetic acid (i) Dissolve 2 g of acetanilide in 2 mL of glacial acetic acid taken

causes severe in a 100 mL beaker.
burns
(ii) Add 4 mL of conc. H2SO4 gradually with stirring to the above
mixture. The mixture becomes hot and clear solution is
Hazard Warning obtained. Cool the reaction mixture in an ice bath maintained
• Acetanilide may cause at 0-5°C.
cyanosis. (iii) Add a cold mixture of 1.0 mL conc. HNO3 and 1.0 mL conc.
H2SO4 to the viscous reaction mixture drop by drop with
constant stirring, so that the temperature of the mixture does
not rise above 10°C.
(iv) Remove the beaker from the ice bath and allow the reaction
mixture to attain room temperature. Let it stand at room
temperature for about 30 minutes. Stir the reaction mixture
continuously and pour it on 100g of crushed ice.
(v) Stir the mixture well and filter the compound so obtained.
108
(vi) Wash the compound with cold water and dry it.
(vii) Recrystallise a small amount of the pale yellow solid from
alcohol. Colourless crystals of p-nitroacetanilide are
obtained. Yellow ortho-nitroacetanilide formed in the small
amount remains dissolved in the mother liquor.
(viii) Record the yield and melting point of the pure compound.
Result
(a) Yield of p-nitroacetanilide is _______ g.
(b) Melting point of p-nitroacetanilide is ______°C.
Precautions
(a) Do not allow the temperature of the reaction mixture to exceed 10°C during
addition of nitrating mixture.
(b) Add mixture of concentrated nitric acid and sulphuric acid into the solution of
acetanilide slowly and carefully.
EXPERIMENT 10.4
Aim
To prepare phenyl–azo–β-naphthol (an azo dye).
Theory
Aniline is an aromatic primary amine. It forms diazonium salt
when treated with nitrous acid at 0-5°C. Nitrous acid is generated
in situ by the reaction of sodium nitrite with hydrochloric acid.
The process is called diazotisation. The diazonium salt is
coupled with an alkaline solution of β-naphthol to form an
orange-red azo dye.
109
Material required
• Aniline : 2 mL
• Beaker (250mL) : One • Conc. HCl : 6.5 mL
• Conical flask (100mL) : One • Sodium nitrite : 1.6 g
• Glass rod : One • β-naphthol : 3.2 g
• Thermometer (210°C) : One • Sodium hydroxide : 2.0 g
• Filter paper : As per need • Glacial acetic acid : 12.0 mL
• Funnel : One • Ice : As per need
• Melting point assembly : One • Distilled water : As per need
Procedure
Aniline
(i) Take 6.5 mL of concentrated hydrochloric acid in a 100 mL
beaker. Dilute it with 6.5 mL of water and dissolve 2 mL of
aniline in it.
(ii) Cool the above mixture by placing the beaker in an ice bath
HCl
maintained at 0-5°C temperature.
(iii) Diazotise the above mixture by adding a solution of 1.6 g of
Sodium
sodium nitrite in 8 mL water.
nitrite (iv) Dissolve 3.2 g β-naphthol in 18 mL of 10% sodium
hydroxide solution. Add about 25 g of crushed ice to it.
Sodium
(v) Stir the β-naphthol solution well and add chilled diazonium
hydroxide chloride solution very slowly to it with constant stirring.
(vi) An orange red dye of phenyl-azo-β-naphthol is formed.
(vii) Allow the mixture to stand in the bath for 30 minutes with
β-naphthol occasional shaking.
(viii) Filter the crystals obtained and wash them well with cold
water.
Acetic acid (ix) Recrystallise about one-fourth of the crude product from
causes severe
burns
glacial acetic acid.
(x) Filter the recrystallised sample, wash with a little alcohol to
remove acetic acid. Dry the recrystallised sample between
the folds of a filter paper.
(xi) Record the yield and the melting point of the compound.
Result
(a) Yield of phenyl–azo–β–naphthol is ______g and its
(b) Melting point of phenyl-azo-β-naphthol is _______ °C.
110
Precautions
(a) Maintain the temperature in the range of 0-5°C during diazotisation.
(b) Always add diazonium chloride solution in alkaline β-naphthol for dye formation
and not vice versa.
(c ) Dry the recrystallised sample perfectly for determining the melting point.
Note : Azo-dye synthesis are mostly so nearly quantitative that one should use amounts of reactants
closely agreeing with equations. Any excess of certain reactants may cause decomposition of
unused material and tar may appear.
EXPERIMENT 10.5
Aim
To prepare aniline yellow (p-amino-azobenzene).
Theory
p-aminoazobenzene can be prepared in a good yield by
rearrangement reaction of diazoaminobenzene with a small
quantity of aniline hydrochloride in the presence of aniline as
solvent. The chemistry of this conversion is as follows:
The above reaction is carried out only in weekly acidic

conditions.
Material Required
• Conical Flask (100 mL) : One • Diazoaminobenzene : 3g

• Thermometer : One • Aniline : 7 mL
• Funnel : One • Aniline hydrochloride : 1.5 g
• Melting point assembly : One • Glacial acetic acid : 9 mL
• Waterbath : One • Carbon tetrachloride : 9 mL
111
Procedure
(i) Dissolve 3 g of finely powdered diazoaminobenzene in 7 mL

Aniline
of aniline in a 100 mL conical flask.
(ii) Add 1.5 g of finely powdered aniline hydrochloride to the
Acetic acid
above mixture.
causes
severe burns (iii) Warm the mixture with occasional shaking on a water bath
at about 40-45°C , for a period of about one hour.
Carbon (iv) Remove the flask from the water bath and allow the reaction
tetrachloride mixture to stand at room temperature for about 30 minutes.
(v) Add 9 mL of glacial acetic acid diluted with an equal volume
of water and shake the reaction mixture thoroughly to
convert excess aniline to its acetate, which is water-soluble.
(vi) Allow the mixture to stand for 15 minutes with occasional
stirring.
(vii) Filter p-aminoazobenzene, wash with a little cold water and
dry between the folds of a filter paper.
(viii) Recrystallise a small portion of crude p-aminoazobenzene
from carbon tetrachloride.
(ix) Report the yield and melting point of p-aminoazobenzene.
Result
Yield of p–aminoazobenzene is ______ g and its melting point
is ____°C.
Precautions
(a) Maintain the temperature of the reaction mixture at about 40-50°C.

(b) Wash the crude product with a small volume of water repeatedly.
(c) Note the melting point of the perfectly dry sample.
AN ALTERNATIVE PROCEDURE FOR PREPARING ANILINE YELLOW
Theory
Aniline yellow can also be prepared by direct diazotisation and
coupling as followed for phenyl-azo-β-naphthol dye. However,
coupling of the diazonium salt with aniline or any other aromatic
amine is carried out in a weakly acidic medium.
112
Material Required
• Funnel : One
• Aniline : 6 mL
• Conical flask (100 mL) : One
• 1.0 M HCl : 4 mL
• Thermometer : One
• Carbon tetrachloride : As per need
Procedure
(i) Prepare a solution of benzene diazonium chloride using 2 mL Aniline
of aniline according to the method described for the preparation
of phenyl-azo–β–naphthol dye (see experiment 10.4). Carbon
(ii) Prepare a solution of 4 mL aniline in 4 mL 1.0 M HCl. tetrachloride
(iii) Add the cold solution of aniline hydrochloride slowly into
the cold solution of benzene diazonium chloride. HCl
(iv) Filter the yellow compound and dry it between the folds of a
filter paper.
(v) Recrystallise the small amount of crude sample from carbon
tetrachloride and report the yield and melting point.
(i) Why is acetic anhydride preferred over acetyl chloride for acetylation reaction?
(ii) In the preparation of p-nitroacetanilide another minor product is formed. What is this
compound and how can this be separated from p-nitroacetanilide?
(iii) Is it necessary to recrystallise the compound obtained from the reaction? Explain why.
(iv) How is an organic compound recrystallised?
(v) What is the role of acetic acid or pyridine in acetylation?
(vi) How is crude solid compound purified?
(vii) Which of the following compounds on diazotisation followed by coupling with β–naphthol
will form an azo dye?
(a) p-Toluidine (b) Benzylamine (c ) N-Methylaniline.
(viii) Why are diazonium chlorides usually soluble in water?
(ix) How is methyl orange prepared in the laboratory?
(x) How can phenol and aniline be distinguished chemically?
(xi) Why is aniline soluble in hydrochloric acid while it is insoluble in water?
(xii) Why is aniline a weaker base than ammonia?
(xiii) In contrast to aromatic primary amines, aliphatic primary amines do not form stable
diazonium salts. Why?
113

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NEET (UG) SYLLABUS FOR PRACTICAL CHEMISTRY

6.1 DETECTION OF END POINT

6.2 REQUIREMENT FOR A REACTION IN THE TITRIMETRIC ANALYSIS

6.3 ACIDIMETRY AND ALKALIMETRY

It is difficult to obtain an ideal primary standard.

6.4 INDICATORS IN ACID BASE TITRATION

(Colourless in acid) (Pink in alkali)

Fig. 6.1 : Phenolphthalein in acidic and basic medium

In the acidic medium, equilibrium lies to the left. In the alkaline

The anion formed from the indicator is an active species, which

Benzenoid form of the anion Quinonoid form of the anion

Fig. 6.2 : Structures of Methyl orange

changes from colourless to pink. This change of colour is easily

In this titration phenolphthalein (HPh) is used as an indicator.

where a1, M1, V1 are respectively basicity, molarity and volume

• Burette (50 mL) : One

(A) Preparation of 0.1M Standard Solution of Oxalic Acid

(i) Clean the burette thoroughly, wash it with distilled water

Note : • Adjust the flow of liquid by the thumb and two

Fig. 6.3 : Titrating the solution

Volume of oxalic Burette readings Volume of sodium

KNOW THIS ALSO

Relationship between Normality and Molarity

• Measuring flask (100 mL) : One

• Burette (50 mL) : One

Volume V1 of Burette readings Volume of HCl

M2 and V2 are the molarity and volume respectively of hydrochloric acid

∴ Concentration (Strength) of HCl solution in g/L = Molarity × Molar mass

KNOW THIS ALSO

Potassium hydrogenphthalate is primary standard for standardisation of sodium hydroxide

Phenolphthalein can be used as an indicator in this titration.

particles remain suspended in solution and coagulation does

• Beaker (250 mL) : One

(ii) Add 2g of ferric chloride/aluminium chloride powder to

Fig. 1.1 : Purification of a colloid

water. The mixing capacity of different oils with water is different.

• Test tubes : Six • Soap/detergent : 5g

Table 1.1 : Emulsification of different oils by soap/detergent

• Beaker (100 mL) : One

time and record the time required for the disappearance of

Note : If thermostat (i.e. constant temperature bath) is not available for

Table 2.1 : Effect of concentration of HCl on the rate of reaction between

Volume of HCl added in mL Time ‘t’ in seconds for the mark

Table 2.2 : The effect of temperature on the rate of reaction between

(i) The reaction under examination is as follows:

• Starch solution : As per need

from flask A. Note the time required for the appearance of

Sl. Composition of the Time taken for appearance of the

1. 25 mL solution from flask A +

2. 25 mL solution from flask A +

3. 25 mL solution from flask A +

(iii) Why does iodine impart blue colour to starch?

The evolved iodine produces blue colour with the starch

• 2 M Sulphuric acid : As per requirement

(ix) Record your observations as given in Table 2.4.

Sl. Time taken for appearance of the Average

1. 25 mL solution from flask A +

4. 25 mL solution from flask A +

(iv) Out of the reactions (1) and (2) given below: