Selfstudys Com File (2)
Selfstudys Com File (2)
ii.
If H2SO4, that is H3O+ ions are added, the hydrolytic equilibrium shifts to the left.
Turbidity of Cu(OH)2 dissolves to give a clear solution. Hence, it is necessary to add
H2SO4 while preparing the solution of CuSO4.
Exercise | Q 2.1 | Page 61
Answer the following in one sentence :
Classify the following buffers into different types :
a. CH3COOH + CH3COONa
b. NH4OH + NH4Cl
c. Sodium benzoate + benzoic acid
d. Cu(OH)2 + CuCl2
Solution:
Buffer Type
i. CH3COOH + CH3COONa Acidic buffer
ii. NH4OH + NH4Cl Basic buffer
iii. Sodium benzoate + benzoic acid
Acidic buffer
ii.
Exercise | Q 3.02 | Page 62
Answer the following in brief :
What is meant by conjugate acid-base pair?
Solution:
i. The base produced by accepting the proton from acid is the conjugate base of that
acid.
ii. Similarly, the acid produced when a base accepts a proton is called the conjugate
acid of that base.
iii. A pair of an acid and a base differing by a proton is said to be a conjugate acid-base
pair.
Solution:
Solution:
ii.
The Na+ ions of salt have no tendency to react with OH− ions of water since the possible
product of the reaction is NaOH, a strong electrolyte.
iii.
iv.
As a result of excess OH− ions produced, the resulting solution of Na2CO3 is alkaline.
v.
Similarly, ammonium chloride (NH4Cl) is salt of strong acid HCl and weak base NH4OH.
When NH4Cl is dissolved in water, it dissociates completely as,
Exercise | Q 3.09 | Page 62
Answer the following in brief :
The pH of a weak monobasic acid is 3.2 in its 0.02 M solution. Calculate its dissociation
constant.
Solution:
Given:
pH of weak monobasic acid = 3.2,
Concentration of solution (c) = 0.02 M
To find: Dissociation constant (Ka)
Formula:
i. pH = -log10[H3O+]
ii. Ka = α2c
Calculation:
From the formula (i),
pH = -log10[H3O+]
∴ log10[H3O+] = -3.2
= - 3 - 0.2 + 1 - 1
= (-3 - 1) + 1 - 0.2
iii.
Suppose 1 mol of acid CH3COOH is initially present in volume V dm3 of the solution. At
equilibrium, the fraction dissociated would be α, where α is the degree of dissociation of
the acid. The fraction of an acid that remains undissociated would be (1 - α).
vi.
If c is the initial concentration of CH3COOH in mol dm–3 and V is the volume in dm3 mol–
1 then c = 1/V. Replacing 1/V in equation (2) by c,
we get
Equation (5) implies that the degree of dissociation of a weak acid (CH3COOH) is
inversely proportional to the square root of its concentration or directly proportional to
the square root of the volume of the solution containing 1 mol of the weak acid.
Exercise | Q 4.02 | Page 62
Answer the following :
Define pH and pOH.
Solution:
i.
The pH of a solution is defined as the negative logarithm to the base 10, of the
concentration of H+ ions in solution in mol dm–3.
pH is expressed mathematically as
pH = -log10[H+] or pH = -log10[H3O+]
ii.
Similarly, pOH of a solution can be defined as the negative logarithm to the base 10, of
the molar concentration of OH− ions in solution.
pOH = -log10[OH-]
Kw = [H3O+][OH-]
-log10[H3O+] + {-log10[OH-]} = 14
∴ pH + pOH = 14
iii. Let the fraction dissociated at equilibrium is α and that remains undissociated is (1 −
α).
vi. If c is the initial concentration of base in mol dm–3 and V is the volume in dm3 mol–
1 then c = 1/V. Replacing 1/V in equation (2) by c,
we get
The degree of dissociation of a weak base is inversely proportional to square root of its
concentration and is directly proportional to square root of volume of the solution
containing 1 mol of weak base.
Solution2:
i. Consider an equilibrium of weak acid HA that exists in solution partly as the
undissociated species HA and partly H+ and A– ions. Then
iii. Suppose 1 mol of acid HA is initially present in volume V dm3 of the solution. At
equilibrium, the fraction dissociated would be α, where α is the degree of dissociation of
the acid. The fraction of an acid that remains undissociated would be (1 − α).
The equation (5) implies that the degree of dissociation of a weak acid is inversely
proportional to the square root of its concentration or directly proportional to the square
root of volume of the solution containing 1 mol of the weak acid.
Exercise | Q 4.06 | Page 62
Answer the following :
Sulfides of the cation of group II are precipitated in acidic solution (H2S + HCl) whereas
sulfides of cations of group IIIB are precipitated in the ammoniacal solution of H 2S.
Comment on the relative values of the solubility product of sulfides of these.
Solution:
Group II and group IIIB cations are precipitated as their sulphides. However, the
solubility product of sulphides of group II cations is lower than group IIIB cations.
Therefore, for the precipitation of cations of group II, only a small concentration of
sulphide ion is required. This is achieved by passing H2S gas in the presence of strong
electrolyte HCl, which has a common ion (H+) with H2S. Due to the common ion effect,
the dissociation of H2S is suppressed and thus, the concentration of S2- ions decreases.
This results only in the precipitation of sulphides of group II while sulphides of the higher
group remain in solution as they require a higher concentration of S2- ions for
precipitation.
Exercise | Q 4.07 | Page 62
Answer the following :
The solubility of a sparingly soluble salt gets affected in the presence of a soluble salt
having one common ion. Explain.
Solution:
i. The presence of a common ion affects the solubility of a sparingly soluble salt.
ii. Consider, the solubility equilibrium of AgCl,
iii. Suppose AgNO3 is added to the saturated solution of AgCl. The salt AgNO3 being a
strong electrolyte dissociates completely in the solution.
iv. The dissociation of AgCl and AgNO3 produce a common Ag+ ion. The concentration
of Ag+ ion in the solution increases owing to complete dissociation of AgNO3.
v. According to Le-Chatelier's principle, the addition of Ag+ ions from AgNO3 to the
solution of AgCl shifts the solubility equilibrium of AgCl from right to left. The reverse
reaction in which AgCl precipitates is favoured until the solubility equilibrium is re-
established.
vi. However, the value of Ksp remains the same since it is an equilibrium constant. Thus,
the solubility of a sparingly soluble compound decreases with the presence of a
common ion in solution.
Condition of precipitation:
The ionic product (IP) of an electrolyte is defined in the same way as solubility product
(Ksp). The only difference is that the ionic product expression contains a concentration
of ions under any condition whereas the expression of Ksp contains only equilibrium
concentrations. If,
ii. IP > Ksp; the solution is supersaturated and hence precipitation of the compound will
occur.
iii. If IP < Ksp, the solution is unsaturated and precipitation will not occur.