7.

EQUILIBRIUM
Reversible and irreversible reactions
A reaction that takes place in only one direction is called an irreversible reaction.
e.g. Reaction between NaOH and HCl
NaOH + HCl → NaCl + H2O
Reversible reactions are those which take place in both directions. i.e. here reactants combined to form
products and the products recombine to form reactants.
E.g. Haber process for the preparation of ammonia
N2(g) + 3H2(g) 2NH3(g)
The process by which reactants are converted to products is called forward reaction and the
process by which products recombine to form reactants is called backward reaction. After sometimes, the
rate of forward reaction becomes equal to the rate of backward reaction and the reaction attains
equilibrium. Thus equilibrium is a state in which the rates of forward and backward reactions are equal.
Equilibrium is dynamic in nature. i.e. at equilibrium the reaction does not stop. The reactant
molecules collide to form products and the product molecules collide to form the reactants and the rates
of these reactions are equal.
Physical equilibrium: Equilibrium involving physical process is called physical equilibrium. E.g. melting of
ice, evaporation of water, dissolution of solids or gases in liquids, sublimation etc.
For example when ice and water are kept in a perfectly insulated thermoflask at 273K and 1 atm
pressure, there exist an equilibrium between ice and water. At this stage, there is no change in the mass
of ice and water. i.e. the rate of transfer of molecules from ice to water and the reverse process are
equal.
H2O(s) H2O(l)
Chemical Equilibrium
Equilibrium associated with chemical reactions is called chemical equilibrium. At equilibrium, the
concentrations of reactants and products are constant.
Consider a hypothetical reaction, A + B C+D
As the reaction proceeds, the concentration of the reactants decreases and that of the products
increases. After sometimes, the two reactions occur at the same rates and an equilibrium state is
reached. This can be illustrated by the following graph.

After the equilibrium is attained, the concentration of the reactants and products become
constant. At equilibrium, the rate of forward reaction (rf) = the rate of backward reaction (rb).
Law of Chemical Equilibrium and Equilibrium Constant
This law was proposed by Guldberg and Waage. It states that at constant temperature, the
product of concentration of the products to that of the reactants, in which each concentration terms is
raised to a power which is equal to the stoichiometric coefficients in the balanced chemical equation, has
a constant value.
 For a general reversible reaction:
A+B C+D

According to the equilibrium law, [C][D] = Kc

[A][B]
Where Kc is called the equilibrium constant.
For a general reaction, aA + bB cC + dD,
c d
Kc = [C] [D]
[A]a[B]b
For the reaction H2 + I2 2HI; Kc = [HI]2
[H2][I2]
For the reaction N2 + 3H2 2NH3; Kc = [NH3]2
[N2][H2]3
Equilibrium constant for the reverse reaction is the inverse of that for the forward reaction. i.e. if the
equilibrium constant for the reaction H2 + I2 2HI is Kc, then that for the reverse reaction
2HI H2 + I2 is 1/Kc.
Equilibrium constant for gaseous reactions
For a reaction involving gases, the concentration terms are replaced by partial pressures.
For example, H2(g) + I2(g) 2HI(g); Kp = P2HI
PH2.PI2
Where Kp is called equilibrium constant in terms of partial pressure, PHI, PH2 and PI2 are the partial
pressures of HI, H2 and I2 respectively.
Relation between Kc and Kp
Consider a general reaction, aA + bB cC + dD
The equilibrium constant in terms of concentration for this reaction is Kc = [C]c[D]d
[A]a[B]b ……… (1)
And the equilibrium constant in terms of partial pressures is Kp = PCc.PDd
PAa.PBb …………(2)
From ideal gas equation, PV = nRT, P = nRT/V = CRT (since n/V = C, the concentration)
Therefore, PA = CART, PB = CBRT, PC = CCRT and PD= CDRT
Substitute these values in equation (2), we get
Kp = [CCRT]c.[CDRT]d
[CART]a[CBRT]b
Or, Kp = CCc.CDd (RT)c+d
CAa.CBb (RT)a+b

Or, Kp = CCc.CDd. [RT](c+d)-(a+b)

CAa.CBb
Or, Kp = Kc.(RT)∆n, where Kc = CCc.CDd
CAa.CBb
And ∆n is the change in no. of moles of gaseous species. i.e. ∆n = no. of moles of gaseous products – no.
of moles of gaseous reactants.
Special cases:
i) If ∆n = 0, then Kp = Kc
ii) If ∆n > 0, then Kp > Kc and
iii) If ∆n < 0, then Kp < Kc
Homogeneous and heterogeneous equilibria
An equilibrium reaction in which all the reactants and products are in the same phase is called
homogeneous equilibrium.
e.g. N2(g) + 3H2(g) 2NH3(g)
2SO2(g) + O2(g) 2SO3(g)
Equilibrium reaction in which the reactants and products are in different phases is called heterogeneous
equilibrium.
e.g. CaCO3(s) CaO(s) + CO2(g)
H2O (s) H2O(l)
Characteristics of Equilibrium constant
The important characteristics of equilibrium constant are:
1. Equilibrium constant is applicable only when the concentrations of the reactants and products
have attained their equilibrium state.
2. The value of equilibrium constant is independent of the initial concentrations of reactants and
products.
3. The value of equilibrium constant depends on temperature.
4. The equilibrium constant for the reverse reaction is the reciprocal of that of the forward reaction.
5. If for the reaction A B, the value of equilibrium constant is K, then for the reaction nA nB,
its value is Kn.
Applications of equilibrium constant
The important applications of equilibrium constant are:
1. Prediction of the extent of a reaction
Greater the value of equilibrium constant, greater will be the concentration of products. In
general,
a) If Kc > 103 (i.e. Kc is very large), the reaction proceeds nearly to completion
b) If Kc < 10-3 (i.e. if Kc is very small), the reaction proceeds rarely.
c) If the value of Kc is in between 103 and 10-3 appreciable concentrations of both reactants and
products are present.
2. Prediction of the direction of the reaction
By knowing the values of Kc and Qc, we can predict the direction of a reaction. The
reaction quotient(Qc) is defined in the same way as the equilibrium constant (Kc) except that the
concentrations in Qc are not necessarily the equilibrium values.
For a general reaction, aA + bB cC + dD, the reaction quotient, Qc = [C]c[D]d
[A]a[B]b
If Qc > Kc, the reaction will proceed in the direction of reactants (reverse direction).
If Qc < Kc, the reaction will proceed in the direction of products (forward direction).
If Qc = Kc, the reaction mixture is at equilibrium.
3. Calculation of equilibrium concentrations
By knowing the value of equilibrium constant, we can calculate the equilibrium concentrations of
reactants and products.
RELATIONSHIP BETWEEN EQUILIBRIUM CONSTANT (Kc), REACTION QUOTIENT (Q) AND
GIBBS ENERGY (G)
The Gibb’s energy change of a reaction is related to the reaction quotient (Q) by the equation:
ΔG = ΔG0 + RT lnQ
0
where, ΔG is standard Gibbs energy.
At equilibrium, ΔG = 0 and Q = Kc, so the equation becomes,
0 = ΔG0 + RT ln Kc
Or, ΔG0 = – RT lnKc
On changing the base, we get ΔG0 = – 2.303RT logKc
We know that for a spontaneous process ΔG should be negative. So the value of Kc should be positive.
Factors affecting equilibrium
The important factors affecting equilibrium are temperature, pressure, concentration and catalyst.
The effect of these factors on equilibrium state can be explained by using Le Chatlier’s Principle.
It states that whenever there is a change in concentration, pressure or temperature of a system at
equilibrium, the system will try to readjust in such a way so as to cancel the effect of that change.
1. Effect of concentration change
If we change the concentration of reactants or products in an equilibrium process, then according
to Le Chatlier’s principle, the system will try to reduce the effect of that change. For this the rate of either
forward or backward reaction changes.
In general, an increase in concentration of reactants increases the rate of forward reaction (i.e. the
equilibrium is shifted to the forward direction) and an increase in concentration of products increase the
rate of backward reaction rate (i.e. the equilibrium is shifted to the backward direction).
For example in the reaction 2SO2(g) + O2(g) 2SO3(g), if we increase the concentration of SO2 or
O2, the system will try to reduce the concentration by shifting the reaction to forward direction.
If we remove SO3 from the reaction mixture, its concentration decreases. Here also to increase the
concentration, the system will shift to the forward direction.
In Haber process for the preparation of ammonia, the amount of ammonia formed can be
increased by increasing the concentration of N2 or H2 or by removing NH3 from the reaction mixture.
2. Effect of temperature change
According to Le Chatlier’s principle, increase in temperature favours endothermic process and
decrease in temperature favours exothermic process. In a reversible reaction, if the forward reaction is
endothermic, the backward reaction will be exothermic.
Eg. N2(g) + 3H2(g) 2 NH3(g); ∆H = -92.38kJ/mol
Here since ∆H is negative, the forward reaction is exothermic. So to increase the production of
NH3, temperature should decrease. At higher temperature, the rate of backward reaction increases. i.e.
the ammonia formed is decomposed to N2 and H2.
3. Effect of pressure change
Pressure has its role only in gaseous reactions. In general an increase in pressure favours the reaction
in which number of moles decreases and vice versa.
Thus in the reaction, N2(g) + 3H2(g) 2 NH3(g), when the pressure increases, the system will try to reduce
the pressure. This can be achieved by shifting the reaction into the direction in which no. of moles
decreases (since pressure is directly proportional to the number of moles). So in this reaction, the
equilibrium will shift to the forward direction.
If the volume of the reaction mixture is halved, the concentration and the partial pressure become
doubled. So the reaction is shifted to the direction in which the number of moles or volume decreases.
4. Effect of catalyst
In an equilibrium reaction, a catalyst increases the rate of both forward and backward reactions
Simultaneously and helps to attain the equilibrium faster. It lowers the activation energy for the forward
and backward reactions by exactly the same amount. It does not affect the equilibrium composition of
the reaction mixture.
Thus in Haber process for the manufacture of ammonia, iron (Fe) acts as the catalyst. In contact process
for the manufacture of sulphuric acid, V2O5 (Vanadium pentoxide) is used as the catalyst for the
conversion of SO2 to SO3.
 5. Effect of inert gas addition
If an inert gas (which does not take part in the reaction) is added to an equilibrium mixture at
constant volume (or at constant pressure), there is no change to the equilibrium. It is because the
addition of inert gas at constant volume (or at constant pressure) does not change the partial pressure or
the concentration of the reactants and the products.
Ionic equilibrium in solution
Equilibrium involving ions is called ionic equilibrium. E.g. dissociation of acetic acid in water.
CH3COOH + H2O CH3COO- + H3O+
Electrolytes and non-electrolytes
Based on the ability to conduct electricity, Michael Faraday divided substances into two –
electrolytes and non-electrolytes.
Electrolytes are substances which conduct electricity in molten state or in solution state.
e.g. All acids, bases and almost all salts
Non- electrolytes are substances which do not conduct electricity in molten state or in solution state.
e.g. sugar, urea etc.
Electrolytes are further classified into two - strong electrolytes and weak electrolytes.
Strong electrolytes are electrolytes which dissociate almost completely in aqueous solution.
E.g. strong acids like HCl, HNO3, H2SO4 etc., strong bases like NaOH, KOH etc. and salts like NaCl, KCl,
Na2SO4, K2SO4, KNO3, NaNO3 etc.
Electrolytes which dissociate only partially in aqueous solution are called weak electrolytes. E.g.
weak acids like CH3COOH, formic acid (HCOOH) etc., weak bases like Mg(OH)2, Ca(OH)2, NH4OH etc. and
some salts like CaSO4, BaSO4 etc.
A weak electrolyte dissociates only partially in aqueous solution and so an equilibrium is formed
between the ions and the unionised molecules. This type of equilibrium involving ions in aqueous solution
is called ionic equilibrium.

Acids, Bases and Salts

Acid – base concepts:
1. Arrhenius concept: According to this concept acids are substances which give hydrogen ion (H+) or
hydronium ion (H3O+) in aqueous solution and bases are substances which give hydroxyl ion (OH-)
in aqueous solution.
e.g. HCl is an acid since it produces H3O+ in aqueous solution.
HCl(l) + H2O(l) H3O +(aq) + Cl-(aq)
e.g. for base is NaOH
NaOH(s) + H2O(l) Na+(aq) + OH-(aq)
Note: H+ ions exist in water as hydronium ions (H3O+)
H+ + H2O H3O+
Limitations: this concept is applicable only to aqueous solutions. Also it could not account for the basicity
of substances like NH3 which do not possess OH- ion.
2. The Bronsted – Lowry concept:
According to this concept acids are proton (H+) donors and bases are (H+) acceptors.
For example in the reaction NH3(l) + H2O(l) NH4+(aq) + OH-(aq)
Here NH3 is a base since it accepts an H ion to form NH4+ and H2O is an acid since it donates an H+
+

ion to form OH- . In the reverse reaction, NH4+ is an acid and OH- is a base.
The acid base pair that differs by only one proton is called a conjugate acid – base pair.
An acid formed from a base is called conjugate acid and a base formed from an acid is called conjugate
base.
 e.g. NH3(l) + H2O(l) NH4+(aq) + OH-(aq)
base acid conj. acid conj. base

In general Acid – H+ → Conjugate base

Base + H+ → Conjugate acid
HCl + H2O H3O+ + Cl-
Acid base conj. acid conj. Base

If the acid is strong, its conjugate base is weak and vice versa. So in the above example Cl- is a
weak conjugate base of the strong acid HCl.
Water can act both as acid and base. So it is an amphoteric substance.
e.g. NH3 + H2O NH4+ + OH-
acid
HNO3 + H2O H3O+ + NO3-
Base
3. Lewis concept:
According to this concept acids are electron pair acceptors and bases are electron pair donors.
Substances which donate electron pair are called Lewis bases and substances which accept electron pair
are called Lewis acids.
Example for Lewis acids are BF3, AlCl3, H+, Co3+, Mg2+ etc.
Example for Lewis bases are NH3, H2O, OH-, Cl-, Br- etc.
For a substance to act as Lewis acid, it should contain vacant orbitals and for a substance to act as
Lewis base, it should contain lone pairs of electrons.
e.g. for acid – base reaction is BF3 + NH3 → BF3←NH3
All cations are Lewis acids and all anions are Lewis bases.
The ionization constant of water (The ionic product of water)
Water is a weak electrolyte and hence it ionizes only partially as:
H2O H+ + OH-
Or, H2O + H2O H3O+ + OH-
The dissociation constant, K = [H+][OH-] or, K = [H3O+][OH-]
[H2O] [H2O]
Or, Kw = [H+][OH-] or, Kw = [H3O+][OH-]
Where Kw is called ionization constant of water or ionic product of water. It is defined as the product of
the molar concentration of hydrogen ion (hydronium ion) and hydroxyl ion in water or in any aqueous
solution.
For pure water at 298K, [H+] = [OH-] = 10-7M.
Therefore, Kw = [H+][OH-] = 10-7 x 10-7 = 10-14M2
The value of Kw is temperature dependent.
By knowing the concentrations of H3O+ and OH- ions, we can predict the nature of an aqueous solution.
If [H3O+] > [OH-], the solution is acidic
If [H3O+] < [OH-], the solution is basic
If [H3O+] = [OH-], the solution is neutral
The pH scale
pH is defined as the negative logarithm of the hydrogen ion or hydronium ion concentration in
moles per litre (i.e. molarity). i.e. pH = - log[H+] or pH = - log[H3O+]
Negative logarithm of hydroxyl ion concentration in mol/L is called pOH.
i.e. pOH = -log[OH-]
For pure water, at 298K (250c), [H+] = 10-7. Therefore pH of pure water is 7.
The pH scale was introduced by Sorensen. It contains numbers from 0 to 14. If the pH is less than 7,
the solution is acidic, if it is greater than 7, it is basic and if it is 7, the solution is neutral.
If the pH is 0, 1, 2 etc., the solution is a strongly acidic and if it is 12, 13, 14 etc, it is strongly basic.
The pH of our blood is 7.4 and that of our saliva is 6.4. So blood is slightly basic and saliva is slightly acidic.
Relation between pH and pOH
We know that Kw = [H+][OH-] = 10-14 at 298K
Taking negative logarithm on both sides:
-logKw = -log[H+] + -log[OH-] = -log 10-14
Or, pKw = pH + pOH = 14
Thus by knowing the pH, we can calculate pOH as pOH = 14 - pH

Ionisation constant of weak acids

Consider a weak acid HX, which ionizes only partially as: HX + H2O H3O+ + X-
Let ‘c’ be the initial concentration of HX and ‘α’ is the degree (extent) of dissociation. (It is the ratio of the
number of moles of the electrolyte dissociated to the total number of moles).
Then, HX(aq) + H2O(l) H3O+(aq) + X-(aq)
Initial concn. c 0 0
Eqm. concn. c(1-α) cα cα
+ -
The dissociation constant, Ka = [H3O ][X ]
[HX]
Where Ka is the dissociation constant of the weak acid.
Or, Ka = cα x cα = cα2
C(1-α) 1-α
Larger the value of Ka, stronger is the acid. The negative logarithm of Ka is called pKa.
i.e. pKa = -logKa.
Greater the value of Ka, smaller will be the value of pKa and stronger will be the acid.
Ionisation constant of weak bases
Consider a weak base MOH, which ionizes partially as: MOH M+ + OH-
Let ‘c’ be the initial concentration of MOH and ‘α’ is the degree of dissociation.
Then, MOH(aq) + H2O(l) M+(aq) + OH-(aq)
Initial concn. c 0 0
Eqm. concn. c(1-α) cα cα
The dissociation constant of weak base, Kb = [M+][OH-]
[MOH]
Or, Kb = cα x cα = cα2
C(1-α) 1-α
Also, -logKb = pKb
As the value of Kb increases, pKb decreases and the basic strength increases.
Relation between Ka, Kb and Kw
For conjugate acid – base pair Ka and Kb are related as: Ka x Kb = Kw
This can be deduced as follows:
NH4+ + H2O NH3 + H3O+; Ka = [NH3][H3O+]
[NH4+]
+ -
NH3 + H2O NH4 + OH ; Kb = [NH4+][OH-]
[NH3]
+ - + -
Net reaction : 2H2O H3O + OH ; Kw = [H3O ][OH ]
 Ka x Kb = [NH3][H3O+] x [NH4+][OH-] = [H3O+][OH-] = Kw
[NH4+] [NH3]
-14
i.e. Ka x Kb = Kw = 10

or, pKa + pKb = pKw = 14

Factors Affecting Acid Strength

The extent of dissociation of an acid and its acidic strength depend on the strength and polarity of
the H-A bond. Weaker the H-A bond, more easily it dissociates to give H+ ion and hence stronger is the
acid. Also, greater the polarity of the H – A bond (when the electronegativity difference between the
atoms H and A increases) the more easily it dissociates and hence greater is the acidity.
In a group, acidity is mainly determined by bond strength. From top to bottom in a group, as the
size of A increases, H-A bond strength decreases and so the acid strength increases. Thus acidic strength
of hydrohalic acids increases in the order: HF < HCl < HBr < HI.
In a period, acidity is mainly determined by polarity of the bond. As the electronegativity of A
increases from left to right in a period, the strength of the acid also increases. So the acidity of hydrides of
second period elements increases in the order: CH4 < NH3 < H2O < HF.
Hydrolysis of Salts and the pH of their Solutions
The interaction of anion or cation or both of a salt with water is known as salt hydrolysis. The
cations (e.g., Na+, K+, Ca2+, Ba2+, etc.) of strong bases and anions (e.g., Cl–, Br–, NO3 –, ClO4– etc.) of strong
acids do not get hydrolyse. So the solutions of salts formed from strong acids and bases (e.g. NaCl, KCl,
NaNO3, KNO3, Na2SO4, K2SO4 etc) are neutral i.e., their pH is 7.
1. Hydrolysis of salt of strong base and weak acid: Sodium acetate (CH3COONa), sodium carbonate
(Na2CO3), potassium cyanide (KCN) etc. are examples for such type of salts. Here only the anion of
the weak base undergoes hydrolysis (since cation of the strong base does not hydrolyse). So the
solution of such salts will be basic. i.e. pH > 7.
pH of such salt solution is given by pH = 7 + ½ (pKa + log C) where C is the concentration of salt.
2. Hydrolysis of salt of weak base and strong acid: NH4Cl, NH4NO3, CuSO4 etc are examples for such
type of solutions. Here only cation of weak base undergoes hydrolysis. So the solution is acidic.
pH of such a solution is given by pH = 7 + ½ (pKb + log C).
3. Hydrolysis of salt of weak base and weak acid: ammonium acetate (CH3COONH4), ammonium
carbonate [(NH4)2CO3] etc. are examples for such type of salts. Here both cation and anion
undergo hydrolysis and hence weak acid and weak base are produced in solution. So the solution
may be neutral, acidic or basic depending upon the relative strength of acid and base formed.
pH of such a solution is given by pH = 7 + ½ (pKa + pKb).
Common Ion Effect
It is the suppression of the dissociation of a weak electrolyte by the addition of a strong electrolyte
containing a common ion. For e.g. consider the dissociation of acetic acid (a weak electrolyte).
CH3COOH(aq) CH3COO-(aq) + H+(aq)
If we add some sodium acetate (CH3COONa) to the above equilibrium reaction, the concentration
of acetate ion increases. Then according to Le-Chatlier’s principle, the equilibrium will shift towards left
or, the rate of forward reaction decreases. i.e. the dissociation rate of acetic acid decreases. This is known
as common ion effect.
Another example is the dissociation of the weak base ammonium hydroxide (NH4OH)
NH4OH(aq) NH4+(aq) + OH- (aq)
If we add some NH4Cl to the above equilibrium process, the concentration of NH4+ increases and hence
the equilibrium shifted to the left. i.e. the dissociation rate of NH4OH decreases.
Buffer Solutions
Solution which resists the change in pH on dilution or with the addition of small amount of acid or
alkali is called Buffer solution. There are two types of buffer solutions – acidic buffer and basic buffer.
Acidic buffer is a mixture of a weak acid and its salt with a strong base. E.g. a mixture of acetic acid
and sodium acetate acts as an acidic buffer around pH 4.75.
Basic buffer is a mixture of a weak base and its salt with a strong acid. E.g. a mixture of NH4OH and
NH4Cl acts as a basic buffer around pH 9.25.
PH of a Buffer solution – Henderson - Hasselbalch Equation
Consider an acidic buffer prepared by mixing a weak acid HA and its conjugate bas A-. The weak acid HA
ionises in water as:
HA + H2O H3O+ + A-
The dissociation constant of weak acid, Ka = [H3O+][A-]
[HA]
Taking –ve logarithm on both sides:
-log Ka = -log[H3O+] + - log[A-] – -log[HA]
Or, -log[H3O+] = -logKa + log[A-] – log[HA]
Or, pH = pKa + log[A-]/[HA]
This equation is known as Henderson-Hasselbalch equation. The equation can be written in general form
as: pH = pKa + log[Salt]/[Acid]
For a basic buffer,
pOH = pKb + log[Salt]/[Base]
or, pH = 14 – [pKb + log[Salt]/[Base]]

Solubility Equilibrium
The solubility of a salt in solvent mainly depends on the lattice enthalpy and solvation enthalpy. As
a general rule, for a salt to be able to dissolve in a particular solvent its solvation enthalpy must be greater
than its lattice enthalpy.
Each salt has its characteristic solubility which depends on temperature. We can classify salts on
the basis of their solubility in the following three categories.

Category I Soluble Solubility > 0.1M

Category II Slightly Soluble Solubility in between 0.01M and 0.1M
Category III Sparingly Soluble Solubility < 0.01M

Solubility Product Constant

Consider the dissociation of a sparingly soluble salt in water. Since it dissolves only partially, there
exists an equilibrium between the undissolved solid and the ions.
e.g. Solution of barium sulphate (BaSO4)
BaSO4 (s) Ba2+(aq) + SO42- (aq)
The equilibrium constant, K = [Ba2+][SO42-]
[BaSO4]
For a pure solid, the concentration remains constant.
Therefore, K.[BaSO4] = [Ba2+][SO42-] Or, Ksp = [Ba2+][SO42-]
Where Ksp is called the solubility product constant or simply the solubility product. It is defined as
the product of the molar concentration of ions of a sparingly soluble salt or in a saturated solution.
If S is the molar solubility of BaSO4, then Ksp = S x S = S2
For a general salt AxBy, its dissociation can be denoted as:
AxBy(s) xAy+ (aq) + yBx- (aq); Ksp = [Ay+]x[Bx-]y
If the concentration in the above equation is not the equilibrium concentration, then Ksp is given by Qsp.
At equilibrium, Ksp = Qsp.
If Ksp > Qsp, the dissolution process occurs and if Ksp < Qsp, the precipitation of the salt occurs.
Solubility product and common ion effect found application in the purification of NaCl. If we take a
saturated solution of NaCl and pass HCl gas through it, then NaCl gets precipitated due to the increased
concentration of Cl- ions. NaCl thus obtained has very high purity.
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