Ionic Equilibrium Bits
Ionic Equilibrium Bits
Ionic Equilibrium Bits
EXERCISE - I
Single Answer Type
pH Calculations of Weak Electrolytes and Strong Electrolytes
1. The pH of 10–7 M of NaOH solution
(a) 7.0 (b) 7.21 (c) 6.79 (d) None
1 1
2. The pH of mixture of (400 mL, M H2SO4) + (400 mL, M HCl) + (200 mL of water) will be
200 100
(a) 2.7 (b) 2.1 (c) 3.1 (d) 1.8
1 1
3. The pH of mixture of (400 mL, M Ba(OH)2) + (400 mL M HCl) + (200 mL of water) will be
200 50
(a) 7.7 (b) 2.4 (c) 2.1 (d) 8.0
4. The percentage degree of dissociation of 0.05 M NH3 at 25ºC in a solution of pH = 10 will be
(a) 0.8 (b) 0.6 (c) 0.2 (d) 0.4
5. Two weak monobasic organic acids HA and HB have dissociation constants as 1.6 × 10–5 and
0.4 × 10–5 respectively at 25ºC. If 500 mL of 1 M solutions of each of these two acids are mixed to
produce 1 litre of mixed solution, the pH of the resulting solution will be
(a) 4.10 (b) 3.72 (c) 2.46 (d) 3.25
6. The pH of a solution which contains 100 mL of 0.1 M HCI and 9.9 mL of 1.0 M NaOH will be
(a) 4.03 (b) 10.96 (c) 7.00 (d) 3.04
7. A solution of HCI has a pH = 5. If one mL of it is diluted to 1 litre, what will be pH of resulting
solution.
(a) 5.0 (b) 6.97 (c) 3.0 (d) None
8. 1 c.c. of 0.1 N HCl is added to 99 CC solution of NaCl. The pH of the resulting solution will be
(a) 7 (b) 3 (c) 4 (d) 1
M M
9. 10 ml of H2SO4 is mixed with 40 ml of H SO . The pH of the resulting solution is
200 200 2 4
(a) 1 (b) 2 (c) 2.3 (d) none of these
10. The compound whose 0.1 M solution is basic is
(a) Ammonium acetate (b) Ammonium chloride
(c) Ammonium sulphate (d) Sodium acetate
11. Which of the following solution will have pH close to 1.0?
(a) 100 ml of M/100 HCl + 100 ml of M/10 NaOH
(b) 55 ml of M/10 HCl + 45 ml of M/10 NaOH
(c) 10 ml of M/10 HCl + 90 ml of M/10 NaOH
(d) 75 ml of M/5 HCl + 25 ml of M/5 NaOH
12. Which of the following expression is not true ?
CHEM ACADEMY 2 Ionic Equilibrium
0.45
Buffer capacity
0.20
0.40
0.15
(a) (b) 0.35
0.10
0.0 0.2 0.4 0.6 0.8 1.0 0.30
0.0 0.2 0.4 0.6 0.8 1.0
a
a
0.55
0.50
Buffer capacity
0.25
Buffer capacity
0.45
0.20
0.40
0.15
(c) 0.35 (d)
0.30 0.10
0.0 0.2 0.4 0.6 0.8 1.0 0.0 0.2 0.4 0.6 0.8 1.0
a a
47. Buffer capacity of a buffer solution is x, the volume of 1 M NaOH added to 100 mL of this solution if
change in the pH by 1 is
(a) 0.1 x mL (b) 10 x mL (c) 100 x mL (d) x mL
48. What is the difference in pH for 1/3 and 2/3 stages of neutralisation of 0.1 M CH3COOH with 0.1 M
NaOH.
(a) 2 log 3 (b) 2 log (1/4) (c) 2 log (2/3) (d) 2 log 2
–10
49. Ka for HCN is 5 × 10 at 25°C. For maintaining a constant pH of 9, the volume of 5 M KCN
solution required to be added to 10 ml of 2M HCN solution is (log 2 = 0.3)
(a) 4 ml (b) 8 ml (c) 2 ml (d) 10 ml
Salt Hydrolysis
50. The pH of 0.4 M aqueous NaCN solution will be (Given pKb of CN– = 4.70)
(a) 2.548 (b) 3.513 (c) 10.123 (d) 11.450
51. The pH of the mixture (25 mL of 0.1 M NH4OH + 25 mL of 0.1 M CH3COOH) will be
Given that Ka : 1.8 × 10–5, and Kb = 1.8 × 10–5
(a) 6 (b) 7 (c) 8 (d) 9
52. Which of the following salts undergoes anionic hydrolysis?
(a) CuSO4 (b) NH4Cl (c) AlCl3 (d) K2CO3.
53. The sodium salt of a certain weak monobasic organic acid is hydrolysed to an extent of 3% in its
CHEM ACADEMY 6 Ionic Equilibrium
0.1M solution at 250C. Given that the ionic product of water is 10−14 at this temperature, what is the
dissociation constant of the acid?
(a) ≈ 1 × 10−10 (b) ≈ 1 × 10−9 (c) 3.33 × 10−9 (d) 3.33 × 10−10
54. The degree of hydrolysis of a salt of weak acid and weak base in it’s 0.1 M solution is found to be
50%. If the molarity of the solution is 0.2 M, the percentage hydrolysis of the salt should be
(a) 100% (b) 50% (c) 25% (d) 10%
55. What is the percentage hydrolysis of NaCN in N/80 solution when the dissociation constant for
HCN is 1.3 × 10–9 and Kw = 1.0 × 10–14
(a) 2.48 (b) 5.26 (c) 8.2 (d) 9.6
56. If equilibrium constant of
CH3COOH + H2O CH3COO– + H3O+ is 1.8 × 10–5, equilibrium constant for
CH3COOH + OH– CH3COO– + H2O is
(a) 1.8 × 10–9 (b) 1.8 × 109 (c) 5.55 × 10–9 (d) 5.55 × 1010
57. The pKa of a weak acid, HA, is 4.80. The pKb of a weak base, BOH, is 4.78. The pH of an aqueous
solution of the corresponding salt, BA, will be
(a) 8.58 (b) 4.79 (c) 7.01 (d) 9.22
Solubility (S) and Solubility Product (Ksp)
58. The solubility of silver oxalate in 10–2 M potassium oxlalate solution given that KSP of silver
oxalate = 10–10 will be :
(a) 10–5 (b) 5 × 10–5 (c) 10–6 (d) None
–10
59. The solubility product of SrF2 in water is 8 × 10 . Its solubility in 0.1 M NaF aqueous solution will
be
(a) 8 × 10–8 (b) 8 × 10–3 (c) 2.8 × 10–5 (d) None
60. The solubility of BaSO4 when CaSO4 and BaSO4 are dissolved in water simultaneously Ksp of
CaSO4 = p, Ksp of BaSO4 = q and solubility of CaSO4 is ‘b’ mol/litre will be
(a) pq/b (b) bq/p (c) pb/q (d) none
61. Which of the following is most soluble in water?
(a) MnS (Ksp= 8×10–37) (b) ZnS (Ksp= 7×10–16)
(c) Bi2S3 (Ksp= 1×10–72) (d) Ag3(PO4) (Ksp= 1.8×10–18)
62. The precipitate of CaF2(Ksp = 1.7 × 10–10) is obtained when equal volumes of the following are
mixed
(a) 10–4 M Ca2+ + 10–4 M F– (b) 10–2 M Ca2+ + 10–3 M F–
(c) 10–5 M Ca2+ + 10–3 M F– (d) 10–3 M Ca2+ + 10–5 M F–
63. The solubility of AgCl in water, 0.01 M CaCl2, 0.02 M NaCl and 0.05 M AgNO3 are denoted by S1,
S2, S3 and S4 respectively. Which of the following relationship is correct?
(a) S1 > S2 > S3 > S4 (b) S1 = S2 = S3 = S4 (c) S1 > S3 > S2 > S1 (d) S1 > S2 = S3 > S4
64. How many moles of NH3 must be added to 2.0 litre of 0.80 M AgNO3 in order to reduce the Ag+
concentration to 5 × 10–8 M. Kf of [Ag(NH3)2+] = 108
(a) 0.4 (b) 2 (c) 3.52 (d) 4
7 Ionic Equilibrium
–1
65. If the solubility of lithium sodium hexafluorido aluminate, Li3Na3 (AlF6)2 is ‘s’ mol lit , its solubility product
is equal to :
(a) 729 s8 (b) 12 s8 (c) 3900 s8 (d) 2916 s8
66. The solubility product Mg(OH)2 in water at 25ºC is 2.56 × 10−13(mol/lt)3 while that of Al(OH)3 is 4.32 ×
10−34 (mol/lt)4. If s1 and s2 are the solubilities of Mg(OH)2 and Al(OH)3 in water in mol/lt at 250C, what is
the ratio, s1/s2 ?
(a) 2 × 105 (b) 2 × 104 (c) 3 × 106 (d) 3 × 103
67. The solubility of CaF2 (Ksp = 3.4 × 10–11) in 0.1 M solution of NaF would be
(a) 3.4 × 10–12 M (b) 3.4 × 10–10 M (c) 3.4 × 10–9 M (d) 3.4 × 10–13 M.
68. The solubility of Ag2CO3 in water at 250C is 1 × 10−4 mole/litre. What is its solubility in 0.01 M Na2CO3
solution? Assume no hydrolysis of CO32− ion occurs.
(a) 6 × 10−6 mole/litre (b) 4 × 10−5 mole/litre (c) 10−5 mole /litre (d) 2 × 10−5 mole/litre
69. The solubility product of BaCrO4 is 2.4 × 10–10 M2. The maximum concentration of Ba(NO3)2 possible
without precipitation in a 6 × 10–4 M K2CrO4 solution is
(a) 4 × 10–7 M (b) 1.2 × 1010 M (c) 6 × 10–4 M (d) 3 × 10–4 M.
70. What is the solubility of Al(OH)3, (Ksp = 1 × 10–33) in a buffer solution pH = 4 ?
(a) 10–3 M (b) 10–6 M (c) 10–4 M (d) 10–10 M.
71. The solubility of Fe(OH)3 would be maximum in
(a) 0.1 M NaOH (b) 0.1 M HCl (c) 0.1 M KOH (d) 0.1 M H2SO4.
72. At 25ºC, the solubility product values of AgCl and AgCNS are 1.8 x 10−10 and 1.6 x 10−11 respectively.
When a solution is saturated with both solids, calculate the ratio [Cl−]/[CNS−] and also [Ag+] in the
solution.
(a) 1.125, 4 × 10−6 M (b) 11.25, 1.4 × 10−5 M
(c) 11.25, 4 ×10−5 M (d) 1.25, 4 × 10−6 M
73. What is the minimum pH when Fe(OH)3 starts precipitating from a solution containing 0.1M FeCl3?
Ksp of Fe(OH)3 = 8 × 10–13 M3
(a) 3.7 (b) 5.7 (c) 10.3 (d) 8.3
–10
74. The solubility product of AgCl is 10 . The minimum volume (in L) of water required to dissolve
1.722 mg of AgCl is (molecular weight of AgCl = 143.5).
(a) 10 lt. (b) 2.2 lt. (c) 1.2 lt. (d) 20 lt.
75. Ksp of AgCl is 1.96 × 10 . 100 mL of saturated AgCl solution is titrated with 1 × 10–5 M NH4 SCN.
–10
Volume of 1 × 10–5 M NH4 SCN required precipitate all Ag+ from saturated AgCl solution as AgSCN
is:
(a) 140 mL (b) 260 mL (c) 70 mL (d) 200 mL
76. When equal volumes of the following solutions are mixed, precipitation of AgCl (Ksp = 1.8 × 10–10) will
occur only with:
(a) 10–4 M (Ag+) and 10–4 M (Cl–) (b) 10–5 M (Ag+) and 10–5 M (Cl–)
CHEM ACADEMY 8 Ionic Equilibrium
(c) 10–6 M (Ag+) and 10–6 M (Cl–) (d) 10–10 M (Ag+) and 10–10 M (Cl–)
77. Ksp of MX4 and solubility of MX4 is S mol/litre is related by
(a) S = [Ksp/256]1/5 (b) S = [128 Ksp]1/4 (c) S = [256 Ksp]1/5 (d) S = [Ksp / 128]1/4
78. The best explanation for the solubility of MnS in dilute HCl is that :
(a) Solubility product of MnCl2 is less than that of MnS
(b) Concentration of Mn2+ is lowered by the formation of complex ions with chloride ions
(c) Concentration of sulphide ions is lowered by oxidation to free sulphur
(d) Concentration of sulphide ions is lowered by formation of weak acid H2S
79. Which of the following statements is correct for a solution saturated with AgCl and AgBr if their solubilities
in moles per litre in separate solutions are x and y respectively ?
(a) [Ag+] = x + y (b) [Ag+] = [Br–] + [Cl–]
(c) [Br–] = y (d) [Cl–] > x.
80. 0.2 millimoles of Zn2+ ion is mixed with (NH4)2 S of molarity 0.02 M. The amount of Zn2+ remains
unprecipitated in 20 mL of this solution would be (Given : KSP ZnS = 4 × 10–24)
(a) 5.2 × 10–22 g (b) 2.6 × 10–22 g (c) 2 × 10–23 g (d) none of these
81. Solubility product of silver bromide is 5.0 × 10–13 . This quantity of potassium bromide (molar mass
taken as 120 g mol–1) to be added to 1 litre of 0.05 M solution of silver nitrate to start the precipitation
of AgBr is :
(a) 1.2 × 10–10 g (b) 1.2 × 10–9 g (c) 6.2 × 10–5 g (d) 5.0 × 10–8 g
pH of amphiprotic salts and pH of anions
82. Approximate pH of 0.1 M aqueous H2S solution when K1 and K2 for H2S at 25oC are 1×10–7 and
1.3 × 10–13 respectively :
(a) 4 (b) 5 (c) 6 (d) 8
83. pH of 0.1M Na2HPO4 and 0.2M NaH2PO4 are respectively : pKa for H3PO4 are 2.2, 7.2 and 12.0.
(a) 4.7, 9.6 (b) 9.6, 4.7 (c) 4.7, 5.6 (d) 5.6, 4.7
84. The first and second dissociation constants of an acid H2A are 1.0 × 10–5 and 5.0 × 10–10 respectively.
The overall dissociation constant of the acid will be
(a) 5.0 × 10–5 (b) 5.0 × 1015 (c) 5.0 × 10–15 (d) 0.2 × 105
85. For ortho phosphoric acid,
H3PO4 (aq) + H2O (aq) H3O+ (aq) + H2 PO−4 (aq) ; Ka1
H2PO4 (aq) + H2O (aq) H3O+ (aq) + HPO24− (aq) ; Ka2
HPO 24− (aq) + H2O (aq) H3O+ (aq) + PO34− (aq) ; Ka3
The correct order of Ka values is :
(a) K a1 > K a 2 < K a3 (b) K a1 < K a 2 < K a3 (c) K a1 > K a 2 > K a3 (d) K a1 < K a 2 > K a3
86. Approximate pH of 0.1 M aqueous H2S solution when K1 and K2 for H2S at 25oC are 1×10–7 and
1.3 × 10–13 respectively :
(a) 4 (b) 5 (c) 6 (d) 8
9 Ionic Equilibrium
87. pH of 0.1M Na2HPO4 and 0.2M NaH2PO4 are respectively : pKa for H3PO4 are 2.2, 7.2 and 12.0.
(a) 4.7, 9.6 (b) 9.6, 4.7 (c) 4.7, 5.6 (d) 5.6, 4.7
88. Pure water is added into the following solutions causing a 10% increase in volume of each. The greatest %
change in pH would be observed in which case (a), (b), (c) or (d) ?
(a) 0.1 M NaHCO3 (b) 0.2 M NaOH
(c) 0.3 M NH3 – 0.2 M NH4+ system (d) 0.4 M CH3COONH4
–
89. Three reactions involving H2PO4 are given below :
(i) H3PO4 + H2O → H3O+ + H2PO4– (ii) H2PO4– + H2O → HPO42– + H3O+
(iii) H2PO4– + OH– → H3PO4 + O2–
In which of the above does H2PO4– act as an acid ?
(a) (ii) only (b) (i) and (ii) (c) (iii) only (d) (i) only
90. In aqueous solution the ionization constants for carbonic acid are
K1 = 4.2 × 10–7 and K2 = 4.8 × 10–11
Select the correct statement for a saturated 0.034 M solution of the carbonic acid.
(a) The concentration of CO32– is 0.034 M.
(b) The concentration of CO32– is greater than that of HCO3–.
(c) The concentration of H+ and HCO3– are approximately equal.
(d) The concentration of H+ is double that of CO32–.
91. If K1 & K2 be first and second ionisation constant of H3PO4 and K1 >> K2 which is incorrect.
(a) [H+] = [ H 2 PO −4 ] (b) [H+] = K1[ H 3PO 4 ] (c) K2 = [HPO −4 − ] (d) [H+] = 3[PO34− ]
EXERCISE - II
One or More Than One Correct Answer Type
1. Out of the following, amphiprotic species is are
(I) HPO32– (II) OH– (III) H2PO4– (IV) HCO3–
(a) I (b) II (c) III (d) IV
2. If K1 & K2 be first and second ionisation constant of H3PO4 and K1 >> K2 which is correct.
(a) [H + ] = [H 2 PO 4− ] (b) [H + ] = K1[H 3 PO 4 ]
(c) K2 = [HPO4–] (d) [H+] = 3[PO43–]
3. Degree of hydrolysis for a salt of strong acid and weak base is
(a) independent of dilution (b) increases with dilution
(c) increases with decrease in Kb of the bases
(d) decreases with decrease in temperature.
4. A solution containing a mixture of 0.05 M NaCl and 0.05 M NaI is taken (Ksp of AgCl = 10–10 and Ksp of
AgI =4×10–16 ). When AgNO3 is added to such a solution.
(a) the concentration of Ag+ required to precipitate Cl– = 2 ×10–9 mol/L.
CHEM ACADEMY 10 Ionic Equilibrium
(b) the concentration of Ag+ required to precipitate I– = 8 × 10–15 mol/L.
(c) AgCl and AgI will be precipitated together.
(d) first AgI will be precipitated.
5. Choose the correct statement
(a) pH of acidic buffer solution decrease if more salt is added.
(b) pH of acidic buffer solution increases if more salt is added.
(c) pH of basic buffer decreases if more salt is added.
(d) pH of basic buffer increases if more salt is added.
6. Which of following can act as buffer ?
(a) NaCl + NaOH (b) Borax + Boric acid
(c) NaH2PO4 + Na2HPO4 (d) NH4Cl + NH4OH.
7. Which of the following will show common ion effect and form a buffer solution ?
(a) CH3COONH4 and CH3COOH (b) NH4Cl + NH4OH
(c) H2SO4 + NaHSO4 (d) NaCl + NaOH.
8. If Ka1 and Ka2 of H2SO4 are 10–2 and 10–6 respectively then
(a) Ka1 > Ka2 because it is easy to abstract H+ from H2SO4 and less easy to abstract H+ from HSO4–
(b) Ka1and Ka2 may be measured in acetic acid.
(c) Ka1 and Ka2 are measured in H2O.
(d) the H+ ion conc. of 0.01 M H2SO4 will be less than 0.02 M.
9. Equal volumes of following solutions are mixed, in which case the pH of resulting solution will be average
value of pH of two solutions.
(a) Aqeous HCl of pH = 2, aqueous NaOH of pH = 12
(b) Aqeous HCl of pH = 2, aqueous HCl of pH = 4
(c) Aqeous NaOH of pH = 12, aqueous NaOH of pH = 10
(d) Aqeous CH3COOH of pH = 5, aqueous NH3 of pH = 9. [Ka (CH3COOH) = Kb (NH3)]
10. 100 ml of 0.5M hydrazoic acid (HN3, Ka = 3.6 x 10−4) and 400ml of 0.1M cyanic acid (HOCN, Ka = 8
x 10−4) are mixed. which of the following is (are) true for the final solution?
(a) [H+] = 10−2 M (b) [N3−] = 3.6 x 10−3 M
(c) [OCN−] = 6.4 x 10−3 M (d) [H+] = 1.4 x 10−2 M
11. Ka values for HA, HB and HD are 10-5, 10-7 and 10-9 respectively. Which of the following will be correct
for decimolar aqueous solutions of NaA, NaB and NaD at 250C?
(a) (pH)NaA < (pH)NaB (b) (pH)NaD < (pH)NaB
(c) (pH)NaA < (pH)NaD (d) (pH)NaB = 7
12. When 0.1 mol arsenic acids (H3AsO4) is dissolved in 1L buffer solution of pH = 8, which of the following
hold good? For arsenic acid K1 = 2.5 x 10−4, K2 = 5 x 10−8, K3 = 2 x 10−13. [‘<<’ sign denotes that the
high concentration is at least more than 100 times the lower one]
11 Ionic Equilibrium
− − 2−
(a) [H3AsO4] << [H2AsO ] 4
(b) [H2AsO ] << [HAsO ]
4 4
−
(c) [HAsO42−] << [H2AsO ] 4
(d) [AsO43−] << [HAsO ]
4
2−
48. What are the concentrations of H+, HSO −4 , SO 24− and H2SO4 in a 0.20 M solution of sulphuric
acid ?
Given :H2SO4 ⎯→ H+ + HSO −4 ; strong
49. What are the concentration of H+, H2C2O4, HC 2O −4 and C 2 O 24− in a 0.1 M solution of oxalic
acid ?
[K1 = 5.9 ×10–2 M and K2 = 6.4 × 10–5 M ]
EXERCISE - IV
Previous Year Questions
17 Ionic Equilibrium
IIT-JAM Previous Year Questions
1. At 25ºC, the solubility product (Ksp) of CaF2 in water is 3.2 × 10–11. The solubility (in mole per kg of
water) of the salt at the same temperature (ignore ion pairing) is
(a) 4.0 × 10–6 (b) 3.2 × 10–4 (c) 2.5 × 10–4 (d) 2.0 × 10–4
2. At 298 K 0.1 mol of ammonium acetate and 0.14 mol of acetic acid are dissolved in 1 L of water. The pH
of the resulting solution is
[Given: pKa of acetic acid is 4.75]
(a) 4.9 (b) 4.6 (c) 4.3 (d) 2.3
3. The minimum concentration of silver ions that is required to start the precipitation of Ag2S (Ksp = 1 × 10–
51) in a 0.1 M solution of S2– is
(a) 5.6 ×10−11 (b) 5.6 ×10−10 (c) 5.6 × 10–10 (d) 2.8 × 10–5
5. The acid dissociation constant (Ka) for HCOOH, CH3COOH, CH2ClCOOH and HCN at 25ºC are 1.8
× 10–4, 1.8 × 10–5, 1.4 × 10–3 and 4.8 × 10–10, respectively. The acid that gives highest pH at the
equivalence point when 0.2 M solution of each acid is titrated with a 0.2 M solution of sodium
hydroxide is
(a) HCOOH (b) CH3COOH (c) CH2ClCOOH (d) HCN
6. If Ksp is the solubility product of a sparingly soluble salt A3X2, then its solubility is
(a) (Ksp/108)1/5 (b) (Ksp)1/5 (c) (Ksp/72)1.5 (d) (Ksp)1/2
7. Solubility product constant (Ksp) of slats of types MX, MX2 and M3X at temperature ‘T’ are
4.0 ×10–8, 3.2 × 10–14 and 2.7 × 10–15, respectively. Solubilities (mol dm–3) of the salts at temperature
‘T’ are in the order
(a) MX > MX2 > M3X (b) M3X > MX2 > MX
(c) MX2 > M3X > MX (d) MX > M3X > MX2
8. The pH of a 1 × 10–8 M HCl solution is close to
(a) 8.0 (b) 7.1 (c) 6.9 (d) 6.0
9. The pH of a 1.0 × 10–3 M solution of weak acid HA is 4.0. The acid dissociation constant Ka is
(a) 1.0 × 10–3 (b) 1.0 × 10–4 (c) 1.0 × 10–5 (d) 2.0 × 10–5
10. The pH of the solution prepared from 0.005 mole of Ba(OH)2 in 100 cc water is
(a) 10 (b) 12 (c) 11 (d) 13
11. The pKa values of H3PO4 are 2.12, 7.21 and 12.67. The pH of a phosphate buffer containing 0.2 M
NaH2PO4 and 0.1 M Na2HPO4 is _____.
12. A 50 mL solution of 0.1 M monoprotic acid (Ka = 1 × 10–5 at 298 K) is titrated with 0.1 M NaOH at
298 K. Calculate the (H+) of the solution after the addition of 50 mL of NaOH at this temperature.
(given: Kw = 1 × 10–14 at 298 K).
CHEM ACADEMY 18 Ionic Equilibrium
13. Calculate the pH of a solution obtained by mixing 50.00 mL of 0.20 M weak acid HA (Ka = 10–5) and
50.00 mL of 0.20 M NaOH at room temperature.
IIT-JEE Previous Year Questions
14. 0.1 mole of CH3NH2 (Kb = 5 × 10–4) is mixed with 0.08 mole of HCl and diluted to one litre. What will be
the H+ concentration in the solution? What will be the H+ concentration in the solution?
(a) 8 × 10–2 M (b) 8 × 10–11 M (c) 1.6 × 10–11 M (d) 8 × 10–5 M
15. Select the correct alternative .
If pKb for fluoride ion at 25° C is 10.83, the ionisation constant of hydrofluoric acid in water at this
temperature is :
(a) 1.74 × 10−5 (b) 3.52 × 10−3 (c) 6.75 × 10−4 (d) 5.38 × 10−2
16. The solubility of A2X3 is y mol dm–3. Its solubility product is
(a) 6 y2 (b) 64 y4 (c) 36 y5 (d) 108 y5
17. The pH of 0.1 M solution of the following salts increases in the order
(a) NaCl < NH4Cl < NaCN < HCl (b) HCl < NH4Cl < NaCl < NaCN
(c) NaCN < NH4Cl < NaCl < HCl (d) HCl < NaCl < NaCN < NH4Cl
18. An aqueous solution of 6.3 g oxalic acid dihydrate is made up to 250 mL. The volume of 0.1 N
NaOH required to completely neutralise 10 mL of this solution is
(a) 40 mL (b) 20 mL (c) 10 mL (d) 4 mL
19. For sparingly soluble salt ApBq, the relationship of its solubility product (Ls) with its solubility (S)
is
(a) Ls = Sp+q, pp. qq (b) Ls = Sp+q, pp. qp (c) Ls = Spq, pp. qq (d) Ls = Spq, (p.q)p+q
20. A solution which is 10 –3 M each in Mn2+, Fe2+, Zn2+ and Hg2+ is treated with 10–16M sulphide ion.
If Ksp, MnS, FeS, ZnS and HgS are 10–15, 10–23, 10–20 and 10–54 respectively, which one will precipitate
first?
(a) FeS (b) MnS (c) HgS (d) ZnS
21. –5
HX is a weak acid (Ka = 10 ). It forms a salt NaX (0.1 M) on reacting with caustic soda. The degree
of hydrolysis of NaX is
(a) 0.01% (b) 0.0001% (c) 0.1% (d) 0.5%
22. 2.5 mL of 2/5 M weak monoacidic base (Kb = 1 × 10–12 at 25°C) is titrated with 2/15 M HCl in water
at 25°C. The concentration of H+ at equivalence point is (Kw = 1 × 10–14 at 25°C)
(a) 3.7 × 10–13 M (b) 3.2 × 10–7 M (c) 3.2 × 10–2 M (d) 2.7 × 10–2 M
23. A sample of AgCl was treated with 5.00 ml of 1.5 M Na2CO3 solution to give Ag2CO3. The remaining
solution contained 0.0026 g of Cl− per litre . Calculate the solubility product of AgCl.
(Ksp Ag2CO3 = 8.2 × 10−12)
24. Given : Ag(NH3)2+ Ag+ + 2 NH3 , Kc = 6.2 × 10−8 & Ksp of AgCl = 1.8 × 10−10 at 298 K .
Calculate the concentration of the complex in 1.0 M aqueous ammonia .
25. What will be the resultant pH when 200 ml of an aqueous solution of HCl (pH = 2.0) is mixed with
300 ml of an aqueous solution of NaOH (pH = 12.0) ?
19 Ionic Equilibrium
26. The solubility of Pb(OH)2 in water is 6.7 × 10−6M. Calculate the solubility of Pb(OH)2 in a buffer solution
of pH = 8.
27. 500 ml of 0.2 M aqueous solution of acetic acid is mixed with 500 mL of 0.2 M HCl at 25°C.
Calculate the degree of dissociation of acetic acid in the resulting solution.
[Ka of acetic acid = 1.8 × 10–5]
28. Will the pH of water be same at 4°C and 25°C ? Explain.
29. 50 mL 0.2 M of HA is titrated with 0.2 M NaOH, calculate the pH at end point. Given
Ka(HA) = 5 × 10–6 and α << 1.
CHEM ACADEMY 20 Ionic Equilibrium
ANSWER KEY
EXERCISE - I
1. b 2. b 3. b 4. c 5. c 6. d 7. b
8. b 9. b 10. d 11. d 12. d 13. b 14. b
15. c 16. c 17. b 18. d 19. c 20. b 21. b
22. c 23. b 24. c 25. d 26. c 27. d 28. d
29. c 30. a 31. d 32. a 33. b 34. a 35. c
36. c 37. c 38. b 39. b 40. a 41. d 42. a
43. b 44. d 45. d 46. b 47. c 48. d 49. c
50. d 51. b 52. d 53. a 54. b 55. a 56. b
57. c 58. b 59. a 60. b 61. d 62. b 63. d
64. d 65. d 66. b 67. c 68. c 69. a 70. a
71. d 72. b 73. c 74. c 75. a 76. a 77. a
78. d 79. b 80. a 81. b 82. a 83. b 84. c
85. c 86. a 87. b 88. b 89. a 90. c 91. d
EXERCISE - II
1. c,d 2. a,b,c 3. b,c,d 4. a,b,d 5. b,c 6. b,c,d 7. a,b
8. a,b 9. a,d 10. a,b 11. a,c 12. a,d 13. a,b,c 14. d
15. c,d 16. a,b,c 17. a,b 18. b,c,d 19. a,b,d 20. b,c,d 21. a,b
22. a,b,d 23. a,b,c,d 24. b,c 25. a,b 26. a,b,c 27. c,d 28. a,b,c
29. b,c 30. b,c 31. b,c 32. a,b,c
EXERCISE - III
1. 11.60 2. (a) 2.85 (b) 3.8 (c) 6.022
–10
3. (i) 0.05% (ii) 4.30 (iii) 2 × 10 mol/L
4. pH = 2.69, [OH–] = 5 × 10–12, [OCl–] = 1 × 10–3, [CH3COO–] = 1 × 10–3.
5. 7.13 × 10–3 M 6. (i) 1.8 × 10–16, (ii) 1.66 × 10–5
7. 10
8. (a) +1, (b) 0.522, (c) 2.87, (d) 11.13 (e) 6.97, (f) 7, (g) 6.01, (h) 6.97, (i) 2.61, (j) 11.30 (k) 9 (l) 1 , (m)
3
9. [OH–] = 9.0 ×10–6 10. 6.6 gm
11. V = 25 ml
12. (i) 0.11515 (ii) 0.2303, Hence Second buffer Solution will be better buffer.
13. (1) pH = 4.57 (2) V = 25 mL 14. [Salt] = 0.4 M and [Base] = 0.2 M
15. 0.05 mol 16. 9.7324
17. [H+]= 7.5×10-3 18. [OH-] = 6.664 × 10-6
19. (i) 2.85, (ii) 4.0969, (iii) 4.5229, (iv) 4.699, (v) 5.301, (vi) 8.699
21 Ionic Equilibrium
–2 – –5
20. pH = 3 21. pH = 9, h = 10 , [OH ] = 10
22. pH = 11.6020, h = 4 × 1011. 23. pH = 4.477
24. 4.0% 25. 5.12 ×10–6 M
26. 4.98 27. 2.37×10–6
28. Kb = 1.8 × 10–5, 5.27 29. Ksp = 33.33.22.(s)8 = 36.4 (s)8 = 2916 s8
30. 108 s5 31. SAgSCN = 8.16 ×10–7 M, SAgBr = 4.08 × 10–7 M
32. [H+] ≥ 0.105 33. 1.4 ×10–4
34. (i) 10–8 (ii) 2.7 × 10–7 (iii) 3.1 × 10–5 35. 1.0 × 10–18 M
36. 1.0×10–5 mol/lit 37. 2.1 × 10–5
38. 4 × 10–7mol/L AgBr, 9 × 10–7 mol/L AgSCN
39. [Ag+] = 6.667 × 10–5M 40. 2.8 × 10–3 M
41. 4.8 × 10–3 mol
42. (i) AgI > AgBr > AgCl (AgI will precipitate first)
(ii) When AgI starts precipitating, [Ag+] = 10–13, [I–] = 10–1, [Cl–] = 10–1, [Br–] = 10–1
When AgBr starts precipitating, [Ag+] = 10–11, [I–] = 10–3, [Cl–] = 10–1, [Br–] = 10–1
When AgCl starts precipitating, [Ag+] = 10–9, [I–] = 10–5, [Cl–] = 10–1, [Br–] = 10–3
43. (a) 8.6, (b) 8.65, (c) 8.56
44. [H+] = 0.024 M, [H2PO4–] = 0.024 M, [H3PO4 ] = 0.1 – 0.024 = 0.076 M, [HPO42–] = 6.2 × 10–8 M,
[PO43–] = 9.3 × 10–19 M
45. [S2–] = 1.43 × 10–19 M, [HS–] = 3.3 × 10–8 M.
46. [S2-] = 2.5 × 10-15
47. [H+] = [H2PO4-] = 5.623 × 10-3, [HPO42-] = 6.8 × 10-8, [PO43-] = 5.441 × 10-18
48. [H+] = 0.2116 M, [HSO4–] = 0.1884 M, [SO42–] 0.0116 M, [H2SO4] = 0 M