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Chemistry For NEET By Prince Sir

IONIC EQUILIBRIUM 10 . The pH of a soft drink is 3.82.


The hydrogen ion concentration
EXERCISE-1 will be:-
1. INTRODUCTION (1) 1.96 × 10 –2 mol L –1
(2) 1.6 × 10 –4 mol L –1
1. HCl............. in water :
(3) 1.96 × 10 –5 mol L –1
(1) Ionized (2) Decompose (4) None of them
(3) Dissociates (4) Associates 11 . 8 g NaOH is dissolved in one litre
of solution, the molarity of the
2. The formula weight of H2SO4 is 98. The
solution is:-
weight of the acid in 400mL of 0.1 M solution
is:- (1) 0.2 M (2) 0.4 M

(1) 2.45 g (2) 3.92 g (3) 0.02 M (4) 0.8 M

(3) 4.90 g (4) 9.8 g 12 . The amount of acetic acid present


in 100 mL of 0.1M solution is
3. Normality of 2M sulphuric acid is:- :-
(1) 2 N (2) 4N (1) 0.30 g (2) 3.0 g
(3) N/2 (4) N/4
(3) 0.60 g (4) None
4. Find out value of log101024 :- 13 . The number of milli equivalents
(1) 3.010 (2) 3.000 of acid in 100 mL of 0.5N HCl
(3) 0.3010 (4) None solution is:-
(1) 50 (2) 100
5. If pH = 3.31, then find out [H+] (Approxy)
(1) 3.39 × 10 -4 (2) 5 × 10 -4 (3) 25 (4) 200

(3) 3.0 × 10 -3 (4) None 14 . If the molar concentration of PbI2


is1.5× 1 0 -3 m o l L -1, the
6. If [OH–] = 5.0 × 10-5 M then pH will concentration of iodide ions in
be :- g ion L -1 is:-
(1) 5 - log 5 (2) 9 + log 5 (1) 3.0 × 10-3 (2)6.0 × 10-3
(3) log 5 - 5 (4) log 5 - 9
(3) 0.3 × 10-3 (4)0.6 × 10-6
7. B a s i c i t y o f H 3P O 3 and H 3P O 2 a r e 15 . Which one of the following has
respectivily :- highest pH:-
(1) 1 and 2 (2) 2 and 3
(1) Distilled water
(3) 3 and 2 (4) 2 and 1
(2) 1 M NH3
8. Which of the following electrolysis (weak)
(3) 1 M NaOH
would give aqueous solution having 3C
anion concentration (4) Water saturated with chlorine

(1) A3B (2) A3B 2 2. OSTWALD'S DILUTION LAW


(3) A2B 6 (4) A3B 4 16 . Order of dissociation of 0.1 N
9. Find out pH of solution having 2 × 10– CH 3COOH is :- (Dissociation
3 moles of OH– ion's in 2 litre solution constant = 1 × 10 -5)
:- (1) 10 - 5 (2) 10 - 4
-3
(1) pH = 3 (2) pH = 3 + log2 (3) 10 (4) 10 - 2

(3) pH = 3-log2 (4) pH = 11

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17 . If  is the degree of dissociation of weak dibasic organic acid and y is
the hydrogen ion concentration, what is the initial concentration of acid :-

(y)1 y( )1


(1) (2) y(  ) – 1 (3) (4) None of them
2 2

18 . The degree of dissociation of acetic acid is given by the expression  = 0.1


× C–1 (where C = concentration of the acid) What is the pH of the solution
:-
(1) 1 (2) 2 (3) 3 (4) 4

19. Ostwald's dilution law is not applicable for strong electrolytes because:-
(1) Strong electrolytes are completely ionised
(2) Strong electrolytes are volatile
(3) Strong electrolytes are unstable
(4) Strong electrolytes often contain metal ions

20. The degree of ionisation of a compound depends upon :


(1) Size of the solute molecules
(2) Nature of the solute molecules
(3) Nature of the container taken
(4) The amount of current passed

21. Find out Ka for 10–2 M HCN acid, having pOH is 10 :-


(1) K a = 10 –4 (2) K a = 10–2
(3) K a = 10 –5 (4) None of them

22 . Which of the following will occur if a 1.0 M solution of a weak acid is


diluted to 0.01 M at constant temperature:-
(1) Percentage ionisation will increase
(2) [H+] will decrease to 0.01M
(3) Ka will increase
(4) pH will decrease by 2 units

23 . The pH of 0.15 M solution of HOCl (Ka


= 9.6 × 10–6) is:-
(1) 4.42 (2) 2.92
(3) 3.42 (4) None

24 . The extent of ionisation increases (weak electrolytes)


(1) With the increase in concentration of solute
(2) On decreasing the temp. of solution
(3) On addition of excess of water to the solution
(4) On stirring the solution vigorously

25 . If Ka of HCN = 4 × 10–10, then the pH of 2.5


× 10–1 molar HCN (aq) is:-
(1) 4.2 (2) 4.7
(3) 0.47 (4) 5.0

26 . The molarity of nitrous acid at which its pH becomes 2.(Ka = 4.5 × 10–4)
:-

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(1) 0.3333 (2) 0.4444
(3) 0.6666 (4) 0.2222
27 . Correct statement for HCN weak acid at 250C temperature.:-
Ka K a  [OH  ]
(1)  = (2)  =
[H  ] Kw
(3) (1) & (2) both (4) K b = C 2

3. EXPLANATION OF WATER
28 . Ionic product of water will increase, if :-
(1) Dissociation the pressure
(2) Add H +
(3) Add OH–
(4) Increase the temperature

29 . For water at 25° C, 2 × 10–7 moles per litre is the correct answer for which
one of the followoing
(1) [H +] + [OH– ] (2) [H + ] 2
(3) [OH – ] 2 (4) [H +] – [OH– ]

30. The pH of 1 N H2O is :-


(1) 7 (2) > 7
(3) < 7 (4) 0

31. At 250C, the dissociation constant for pure water is given by :-

1  10 1 4
(1) (55.4 × 10 14 ) -1 (2) 1 × 10 -14 (3) (4) None of
18
these

32. Ionic product of water is equal to :-


(1) Dissociation constant of water × [H2O]
(2) Dissociation constant of water × [H+]
(3) Product of [H2O] and [H+]
(4) Product of [OH–]2 and [H+]

33. Addition of H+ and OH– ion's concentration at 900C


(1 ) 10 - 1 4 (2 ) 10 - 1 2
(3) 2 × 10 -6 (4) 2 × 10 -7

34 . The units of ionic product of water (KW) are:-


(1) mol –1 L –1 (2) mol 2– L –2
(3) mol 2– L –1 2
(4) mol L –2

35 . At 900C, pure water has [H3O+] =10–6.7 mol L–1 what is the value of KW at
90 0C:-
(1) 10 –6 (2) 10 –12
(3) 10 –67 (4 ) 10 –13 .4

36 . At 373 K, temp. the pH of pure H2O can be:-


(1) < 7 (2) > 7

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(3) = 7 (4) = 0

37 . Choose the correct relation:-


pH  pOH
(1) = 7 (2) pH + pOH = 14
14
(3) pOH = 14 + pH (4) pH = 14 + pOH

38. The common ion effect is shown by which of the following sets of solutions
:-
(1) BaCl2 + BaNO3 (2) NaCl + HCl
(3) NH4OH + NH4Cl (4) None

39 . Basic strength of NH4OH in presence of NH4Cl


(1) Increases
(2) Remains unchanged
(3) Decreases
(4) Some times increases or sometimes decreases

40 . Which of the following is a true statement :


(1) The ionisation constant and ionic product of water are same.
(2) Water is a strong electrolyte.
(3) The value of ionic product of water is less than that of its ionisation
constant.
(4) At 298K, the number of H+ ions in a litre of water is 6.023 × 1016.

41 . If it is known that H2S is a weak acid and it is ionised into 2H+ and S–
2
. Then in this solution HCl is added so, pH becomes less, then what will
happen :-
(1) Decrease in S–2 ion concentration
(2) Concentration of S–2 is not affected
(3) Increase in S–2 ion concentration
(4) It is not possible, to add HCl in solution

4. SALTS, TYPES OF SALT & CONJUGATE THEORY


42. Which of the following is not an acidic salt :-
(1) NaHSO4 (2) HCOONa
(3) NaH 2PO 3 (4) None of them

43 . Which is a basic salt :–


(1) PbS (2) PbCO3
(3) PbSO4 (4) 2PbCO 3 Pb(OH) 2

44 . The process of neutralisation invariably results in the production of :-


(1) H+ ions
(2) OH— ions
(3) Both H+ and OH— ions
(4) Molecules of water

45. Which of the following is an acid salt :-

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(1) Na2S (2) Na 2SO 3
(3) NaHSO3 (4) Na 2SO 4
5. HYDROLYSIS OF SALTS
0
46 . At 90 C, the pH of 0.1M NaCl aqueous solution is :-
(1) < 7 (2) > 7
(3) 7 (4) 0.1

47 . What will the pH of 1.0 M ammonium formate solution, If Ka=1 × 10–4 acid Kb
=1× 10–5:-
(1) 6.5 (2) 7.5 (3) 8.0 (4) 9.0

48 . Which salt will not hydrolysis :-


(1) KCl (2) Na 2SO 4
(3) NaCl (4) All

49 . Maximum efficiency of cationic hydrolysis will be shown by :-


(1) A + 3 (2) Ga +3
(3) T + 1 (4) T + 3
50 . HCOO– + H2O ‡ˆ ˆ†
ˆˆ HCOOH + OH– is related:-

Kh
(1) h = Kh (2) h =
C

Kh
(3) h = (4) Kh = hc
V

51 . The pH of aqueous solution of sodium acetate is


(1) 7 (2) Very low
(3) > 7 (4) < 7

52 . If pKb for CN– at 25oC is 4.7. The pH of 0.5M aqueous NaCN solution is :-
(1) 12 (2) 10
(3) 11.5 (4) 11

53. The highest pH value is of :-


(1) 0.1 M NaCl (2) 0.1 M NH4Cl
(3) 0.1 M CH3COONa(4) 0.1 M CH3COONH4

54 . pH of K2S solution is:-


(1) 7 (2) Less than 7
(3) More than 7 (4) 0
55 . For anionic hydrolysis, pH is given by:-
1 1 1
(1) pH = pKW - pKb - logc
2 2 2
1 1 1
(2) pH = pKW + pKa – pKb
2 2 2

1 1 1
(3) pH = pKW + pKa + logc
2 2 2
(4) None of above

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56 . A weak acid react with strong base, ionisation constant of weak acid is 10–
4. Find out equilibrium constant for this reaction :-

(1) 10 –10 (2) 10 10


(3) 10 –9 (4) 109

57 . Hydroxyl ion concentration [OH—] in the case of sodium acetate can be expressed
as (where Ka is dissociation constant of CH3COOH and C is the concentration
of sodium acetate):-

(1) [OH –] = (CK w. K a) 1/2(2) [OH–] = C.Kw K a

1/ 2
 C. K w 
(3) [OH–] =   (4) [OH–] = C. Ka. Kw.
 Ka 

58 . Consider :-
(a) FeCl3 in water - Basic
(b) NH4Cl in water - Acidic
(c) Ammonium acetate in water - Acidic
(d) Na2CO3 in water - Basic
Which is/are not correctly matched:-
(1) b and d (2) b only
(3) a and c (4) d only

59 . Which of the following salts undergoes hydrolysis in water:-


(1) Na 3PO 4 (2) CH3COONa
(3) NaNO3 (4) Both of (1) and (2)

60 . A salt 'X' is dissolved in water of pH = 7. The resulting solution becomes


alkaline in nature. The salt is made up of:-
(1) A strong acid and strong base
(2) A strong acid and weak base
(3) A weak acid and weak base
(4) A weak acid and strong base

61 . Ka for cyano acetic acid is 3.5 × 10–3. Then the degree of hydrolysis of
0.05 M. sodium cyano acetate solution will have the following value :-
(1) 4.559 × 10–6 (2) 5.559 × 10–6
(3) 6.559 × 10–6 (4) 7.559 × 10–6

N
62 . Degree of Hydrolysis of solution of KCN is (Given Ka = 1.4  10–9)
1 00

(1) 2.7  10 –3 (2) 2.7  10 –2


(3) 2.7  10 –4 (4) 2.7  10 –5
6. SOLUBILITY & SOLUBILITY PRODUCT(K sp )
63 . The solubility product of sparingly soluble univalent salt is defined as the
product of ionic concentration in a:-
(1) 1 M solution

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(2) Concentration solution
(3) Very dilute solution
(4) Saturated solution

64 . In solubility of salts M2X, QY2 and PZ2 equal, then the relation between their
Ksp will be :-
(1) K sp ( M 2 X ) > K sp ( Q Y 2) > K sp ( P Z 2)
(2) K sp ( M 2 X ) = K sp ( Q Y 2) < K sp ( P Z 2)
(3) K sp ( M 2 X ) > K sp ( Q Y 2) = K sp ( P Z 2)
(4) K sp ( M 2 X ) = K sp ( Q Y 2) = K sp ( P Z 2)

65 . The expression of solubility product of mercurous iodide is :-


(1) [2 Hg + ] 2 × 2 [I – ] 2(2) [Hg ++ ] 2 × [ 2I – ] 2

(3) [ Hg 22  ] × [I – ] 2(4 ) [H g 2+ ] 2 × [ I –] 2

66 . At 250C, the Ksp value of AgCl is 1.8 × 10–10. If 10–


5
moles of Ag+ are added to solution then Ksp will be :-
(1) 1.8 × 10 –15 (2) 1.8 × 10 –10
(3) 1.8 × 10 –5 (4) 18 × 10 +10

67 . At 250C, required volume of water, to dissolve 1g BaSO4 (Ksp = 1.1 × 10–


10
) will be:-
(1) 820 L. (2) 1 L.
(3) 205 L. (4) 430 L.

68 . Concentration of Ag+ ions in saturated solution of Ag2CrO4 at 200C is 1.5


× 10 –4 mol L –1. At 20 0C, the solubility product of Ag 2CrO 4 is :-
(1) 3.3750 × 10 –12(2) 1.6875 × 10 –10
(3) 1.68 × 10 –12 (4) 1.6875 × 10 –11

69 . How many grams of CaC2O4 will dissolve in distilled water to make one litre
saturated solution? solubility product of CaC2O4 is 2.5 × 10–9 mol2 L–2 and
its molecular weight is 128.
(1) 0.0064 g (2) 0.0128 g
(3) 0.0032 g (4) 0.0640 g

70. If the concentration of CrO42- ion in a saturated solution of silver


chromate will be 2 × 10-4 M, solubility product of silver chromate will
be -
(1) 4 x 10 -8 (b) 8 x 10 -12
(3) 32 x 10 -12 (4) 6 x 10 -12

71 . If the solubility of AgCl (formula mass=143) in water at 25°C is 1.43 10–


4
g/100 mL of solution then the value of Ksp will be :–
(1) 1  10 –5 (2) 2  10 –5
(3) 1  10 –1 0 (4) 2  10 –1 0

72. If the salts M2X, QY2 and PZ3 have the same solubilities, their Ksp values
are related as - (S < 1)
(1) K sp (M 2X) = K sp (QY 2) < K sp (PZ 3 )

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(2) K sp (M 2X) > K sp (QY 2) = K sp (PZ 3 )
(3) K sp (M 2X) = K sp (QY 2) > K sp (PZ 3 )
(4) K sp (M 2X) > K sp (QY 2) > K sp (PZ 3 )

73. The solubility product of As2S3 is given by the expression :-


(1) K sp = [As 3+ ] × [S –2 ](2) K sp = [As 3+ ] 1 [S –2 ] 1
(3) K sp = [As 3+ ] 3 [S –2 ] 2(4) K sp = [As 3+ ] 2 [S –2 ] 3

74. If the solubility of PbBr2 is 'S' g molecules per litre, considering 100%
ionisation its solubility product is :-
(1) 2S3 (2) 4S2
(3) 4S3 (4) 2S4

75. If the solubility of lithium sodium hexeafluoro aluminate Li3Na3(AlF6)2 is


'S' mol L–1. Its solubility product is equal to :-
(1) S8 (2) 12 S3
(3) 18S3 (4) 2916 S8

76 . One litre of saturated solution of CaCO3 is evaporated to dryness, when 7.0


g of residue is left. The solubility product for CaCO3 is:-
(1) 4.9 × 10–3 (2) 4.9 × 10–5
(3) 4.9 × 10–9 (4) 4.9 × 10–7

7. APPLICATION OF SOLUBILITY PRODUCT(K sp )

77 . At 300C, In which of the one litre solution, the solubility of Ag2CO3 (solubility
product = 8 × 10–12) will be maximum :-
(1) 0.05 M Na 2CO 3 (2) Pure water
(3) 0.05 M AgNO3 (4) 0.05 M NH3

78 . Solubility of AgBr will be minimum in :-


(1) Pure water (2) 0.1 M CaBr2
(3) 0.1 M NaBr (4) 0.1 M AgNO3

79 . In which of the following, the solution of AgSCN will be unsaturated :-


(1) [Ag + ] [SCN – ] = K sp(2) [Ag +] × [SCN –] < K sp
+ – + – 2
(3) [Ag ] × [SCN ] > K sp(4) [Ag ] [SCN ] < K sp

80 . Correct order of solubility porduct is :-


(1) CaCrO 4 > SrCrO 4 > BaCrO 4
(2) BaCrO 4 > SrCrO 4 > CaCrO 4
(3) CaCrO 4 > BaCrO 4 > SrCrO 4
(4) SrCrO 4 > BaCrO 4 > CaCrO 4

81 . If 's' and 'S' are respectively solubility and solubility product of a sparingly
soluble binary electrolyte then :–
(1) s = S (2) s = S2

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1
(3) s = S 1/2 (4) s = S
2

82 . The solubility product of CuS , Ag2S and HgS are 10–37, 10–44 and 10–54 respectively.
The solubility of these sulphides will be in the order
(1) HgS > Ag2S > CuS(2) Ag2S > HgS > CuS
(3) CuS > Ag2S > HgS(4) Ag2S > CuS > HgS

83. If the maximum concentration of PbCl2 in water is 0.01 M at 298 K, Its


maximum concentration in 0.1 M NaCl will be:-
(1) 4 × 10–3 M (2) 0.4 × 10–4 M
(3) 4 × 10–2 M (4) 4 × 10–4 M

84. M2SO4 (M+ is a monovalent metal ion) has a Ksp of 1.2 × 10–5 at 298 K. The
maximum concentration of M+ ion that could be attained in a saturated solution
of this solid at 298 K is :-
(1) 3.46 × 10–3 M(2) 2.89 × 10–2 M
(3) 2.8 × 10–3 M (4) 7.0 × 10–3 M

85. Which of the following has maximum solubility (Ksp value is given in brackets)
:-
(1) HgS (1.6 × 10–54)(2) PbSO4 (1.3 × 10–8)
(3) ZnS (7.0 × 10–26) (4) AgCl (1.7 × 10–10)

86. Maximum soluble is :- (Ksp is given)


(1) CuS (8.5 × 10–36)(2) CdS (3.6 × 10–28)
(3) ZnS (1.2 × 10–28)(4) MnS (1.4 × 10–10)

87. In which of the following, the solubility of AgCl will be maximum :-


(1) 0.1 M AgNO3 (2) Water
(3) 0.1 M NaCl (4) 0.1 M KCl
88. The solubility product of three sparingly soluble salts are given below :
No . Formula Solubility product
1 PQ 4.0 × 10 –20
2 PQ 2 3.2 × 10 –14
3 PQ 3 2.7 × 10 –35
The correct order of decreasing molar solublity is:-
(1) 1, 2, 3 (2) 2, 1, 3
(3) 3, 2, 1 (4) 2, 3, 1

89 . Ksp value is more for :-


(1) CuS (2) NiS (3) PbS (4) CdS

90 . The Ksp value for Gd(OH)3 is 2.8 × 10–23, the pH at which Gd(OH)3 begins to
precipitate is:-
(1) 6.08 (2) 5.08 (3) 8.47 (4) 4.08

91 . If the solubility product of AgBrO3 and Ag2SO4 are 5.5 × 10–5 and 2 × 10–
5 respectively, the relationship between the solubilities of these can be correctly

represented as:-

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(1) sAgBrO3 > sAg2SO 4(2) sAgBrO3 = sAg2SO 4
(3) sAgBrO3 < sAg2SO 4(4) sAgBrO3 = sAgSO4

92 . 0.5 M HCl solution has ions- Hg++, Cd++ , Sr++, Fe++, Cu++. To pass the H2S
gas in this solution, which are precipitated out :-
(1) C d +2, F e +2, S r + 2( 2 ) C d +2, H g +2, C u +2
(3) H g +2, C u +2, F e + 2( 4 ) C u +2, S r +2, F e +2

93 . Solubility product of Mg(OH)2 is 1 × 10–11. At what pH, precipitation of


2+
Mg(OH)2 will begin from 0.1 M Mg solution :-
(1) 9 (2) 5 (3) 3 (4) 7

94 . In the qualitative analysis of group III, Fe(OH)2 is not precipitated because


:-
(1) The Ksp for Fe(OH)2 is higher
(2) To precipitate Fe(OH)2, only small [OH–] is needed
(3) Fe(OH)2 is a weak electrolyte
(4) The oxidation state of Fe in Fe(OH)2 is +2

95. A solution, containing 0.01 M Zn+2 and 0.01 M Cu2+ is saturated by passing
–2
H2S gas. The S concentration is 8.1 × 10–21 M, Ksp for ZnS and CuS are
–22
3.0 × 10 and 8.0 × 10–36 respectively. Which of the following will occur
in the solution:-
(1) ZnS will precipitate
(2) CuS will precipitate
(3) Both ZnS and CuS will precipitate
(4) Both Zn2+ and Cu2+ will remain in the solution

96. Consider (1) Zn(OH)2 (2) Cr(OH)3 (3) Mg(OH)2 (4) Al(OH)3 which hydroxide
is precipitated by NH4OH containing NH4Cl :-
(1) 1, 2 (2) 2, 4
(3) Only 4 (4) 1, 2, 3 and 4

97 . What will happen if the pH of the solution of 0.001 M Mg(NO3)2 solution is adjusted
to pH = 9
(K sp Mg(OH) 2 = 8.9 × 10 -12 )
(1) ppt will take place
(2) ppt will not take place
(3) Solution will be saturated
(4) None of these

98. The solubility product constant Ksp of Mg(OH)2 is 9.0 × 10-12. If a solution
is 0.010 M with respect to Mg2+ ion, what is the maximum hydroxide ion concentration
which could be present without causing the precipitation of Mg(OH)2 :-

(1) 1.5 × 10-7 M (2) 3.0 × 10-7 M


(3) 1.5 × 10-5 M (4) 3.0 × 10-5 M

99. When HCl gas is passed through a saturated solution of common salt, pure NaCl is
precipitated because:-

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(1) The impurities dissolve in HCl
(2) HCl is slightly soluble in water
(3) The ionic product [Na+] × [Cl–] exceeds the solubility product of NaCl
(4) The solubility product of NaCl is lowered by Cl– from aq. HCl

100. A solution is a mixture of 0.06 M KCl and 0.06 M KI. AgNO3 solution is being
added drop by drop till AgCl starts precipitating (Ksp AgCl = 1× 10–10 and
Ksp AgI = 4 × 10–16). The concentration of Iodide ion at this stage will be
nearly equal to :-
(1) 4.0 × 10–5 M (2) 2.4 × 10–7 M
(3) 2.0 × 10–8 M (4) 4 × 10–8 M

101. Why only As3+ gets precipitated as As2S3 and not Zn2+ as ZnS when H2S is
passed through an acidic solution containing As3+ and Zn2+ :-
(1) Enough As3+ are present in acidic medium
(2) Zinc salt does not ionise in acidic medium
(3) Solubility product of As2S3 is less than that of ZnS
(4) Solubility product changes in presence of an acid

102. H2S is passed through a solution of cations in HCl medium to precipitate cation
of :-
(1) II-A group of cation analysis
(2) II - B group of cation analysis
(3) IV group of cation analysis
(4) Both II - A and II-B gps.

103. To have more sulphide ion concentration, H2S should be passed through :-
(1) 1 N HCl solution
(2) 0.1 M HCl solution
(3) A neutral solution such as water
(4) An ammonical solution

104. When excess oxalic acid is added to CaCl2, CaC2O4 is precipitated and the
solution still contains some unprecipitated Ca2+ for the reason:-
(1) CaC2O4 is a soluble salt
(2) Oxalic acid does not ionise at all
(3) When H2C2O4 is added to CaCl2, HCl is formed which is
fully ionised and thus increases the H+ ion concentration so supresses
the ionisations of H2C2O4 and hense the ionic product of CaC2O4 is not
exceeded to the solubility product
(4) None of the above

105. The solubility product of hydroxides of Mg+2, Zn+2, and Fe+3 decreases as
Ksp Mg(OH)2 > Ksp Zn(OH)2 > Ksp Fe(OH)3 The order of precipitation of hydroxides
is:-

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(1) Fe(OH)3, Zn(OH)2, Mg(OH)2
(2) Mg(OH)2, Zn(OH)2, Fe(OH)3
(3) Zn(OH)2, Fe(OH)3, Mg(OH)2
(4) Zn(OH)2, Mg(OH)2, Fe(OH)3
8. FEW IMPORTANT POINTS
10 6. Two monobasic weak acids have the same concentration of H+ ions. What is
the relationship between dissociation constant and dilution:-
(1) Ka 1 V1  Ka 2 V2 (2) Ka 1 V2  Ka 2 V1
1 1
(3) Ka 1 V1  2  Ka 2 V2 (4) Ka 1 V1 Ka 2 V2  2
 

10 7. What is the molar concentration of chloride ion for the solution obtained by
mixing 300 mL of 3.0M NaCl and 200 mL of 4.0 M solution of BaCl2 :-
(1) 5.0 M (2) 1.8 M
(3) 1.6 M (4) None of these

108. The pH of a 0.1 M formic acid 0.1% dissociated is equal to 4. What will
be the pH of another weak acid (same concentration) which is 1% dissociated
(1) 2 (2) 3 (3) 1 (4) 4

72 E
Chemistry For NEET By Prince Sir

ASSERTION & REASON QUESTIONS


These questions consist of two statements each, printed as Assertion
and Reason. While answering these Questions you are required to choose
any one of the following four responses.
A . If both Assertion & Reason are True & the Reason is a correct explanation
of the Assertion.
B . If both Assertion & Reason are True but Reason is not a correct
explanation of the Assertion.
C . If Assertion is True but the Reason is False.
D . If both Assertion & Reason are False.
1 . Assertion :– When small amount of insoluble in dilute HCl.
acid or base is added to pure water, Reason :– MnS and ZnS are precipitated
its pH undergoes a change. in presence of dilute HCl.
Reason :– Addition of an acid or 7 . Assertion :– If Ksp < ionic product,
base increases the degree of precipitate is formed.
ionisation of water. Reason :– Solubility product (Ksp)
2 . Assertion :– A very dilute acidic is the highest limit of ionic product
solution of Cd2+ and Ni2+ gives yellow of the electrolyte in saturated
precipitate of CdS on passing hydrogen solutions.
sulphide. 8. Assertion :– To precipitate the
Reason :– Solubility product of CdS cations of fourth group in qualitative
is more than that of NiS. analysis, medium is made alkaline
3 . Assertion :– The pH of an aqueous before passing H2S gas.
solution of acetic acid remains
unchanged on the addition of sodium Reason :– This is done to suppress
acetate. the ionisation of H2 S.
Reason :– The ionisation of acetic 9. Assertion :– When an acid or a base
acid is suppressed by the addition is
of sodium acetate.
added to water at constant temperature
4 . Assertion :– If HCl gas is passed
the pH changes.
through saturated NaCl solution, solid
NaCl starts to precipitate. Reason :– This is due to change in
Reason :– HCl decreases the ionic product of water.
solubility product of NaCl. 10. Assertion :– Addition of silver ions
5 . Assertion :– Heat of ionisation of
to a mixture of aqueous sodium chloride
water is equal to the heat of and sodium bromide solution will first
neutralisation of a strong acid with
precipitate AgBr rather than AgCl.
a strong base.
Reason :– Water ionises to a very Reason :– Ksp of AgCl < Ksp of AgBr.
small extent while H+ ions from acid 11 . Assertion :- BaCO3 is more soluble
combine very rapidly with OH– from in HNO3 than in plain water.
base to form H2O.
6 . Assertion :– Both ZnS and MnS are Reason :- Carbonate is a weak base
and reacts with the H+ from the strong
acid causing the barium salt to
dissociate.
ASSERTION & REASON QUESTIONS
12. Assertion ANSWER
: Addition of NH4KEY
OH to
an aqueous solution of BaCl2 in the
Qu e. 1 2 3 4 5 6 7 8 p r9e s e n10
c e 11o f 12 N H13
4
Cl(excess)
An s. C C D C D D A C precipitates
C C C Ba(OH) .
D 2 D
Reason : Ba(OH)2 is insoluble in
E water. 73
13. A s s e r t i o n :– Sb(III) is not
Chemistry For NEET By Prince Sir

BUFFER SOLUTIONS AND INDICATOR EXERCISE–4


1. A solution of H3BO3 and borax is 8. Phenolphthalein does not act as an
called :- indicator for the titration between
(1) Acidic buffer (2) Basic buffer :-
(3) Basic solution(4) None of these (1) KOH and H2SO 4
(2) NaOH and CH3COOH
2. In a buffer solution the ratio of
(3) Oxalic acid and KMnO4
concentration of NH4Cl and NH4OH is
1 : 1 when it changes in 2 (4) Ba(OH)2 and HCl
: 1 what will be the value of pH 9. Which can act as buffer :-
of buffer :- (1) NH4OH + NaOH
(1) Increase (2) Decrease (2) HCOOH + CH3COONa
(3) No effect (4) N.O.T.
(3) 40 mL 0.1 M NaCN + 20 mL of 0.1
3. To a 50 mL of 0.05M formic acid how M HCl
much volume of 0.10M sodium formate (4) None of them
must be added to get a buffer solution
of pH = 4.0 ? (pKa of the acid is 10. The buffer solution play an important
3.8) role in :-
(1) 50 mL (2) 4 mL (1) Increasing the pH value
(3) 39.6 mL (4) 100 mL (2) Decreasing the pH value

4. In the volumetric estimation of HCl, (3) Keeping the pH constant


if we make use of phenolphthalein as (4) Solution will be neutral
an indicator, which base is unsuitable
for the titration :- 11. Ka for HCN is 5 x 10–10 at 250C.
For maintaining a constant pH of 9,
(1) NaOH (2) RbOH
the volume of 5M KCN solution required
(3) KOH (4) NH4OH
to be added to 10mL of 2M HCN solution
5. In a mixture of weak acid and its is-
salt, the ratio of concentration of (1) 4 mL (2) 7.95 mL
acid to salt is increased ten-fold.
(3) 2 mL (4) 9.3 mL
The pH of the solution :-
(1) Decreases by one 12 . Buffering action of a mixture of
(2) Increases by one-tenth CH3COOH and CH3COONa is maximum when
(3) Increases by one the ratio of salt to acid is equal
(4) Increases ten-fold to -
(1) 1.0 (2) 100.0
6. pKb for NH4OH at certain temperature
(3) 10.0 (4) 0.1
is 4.74. The pH of basic buffer
containing equimolar concentration of 13 The pink colour of phenolphthalein
NH4OH and NH4Cl will be:- in alkaline medium is due to -
(1) 7.74 (2) 4.74
(1) Negative ion (2) Positive ion
(3) 2.37 (4) 9.26
(3) OH– ions (4) Neutral form
7. What is the suitable indicator for
14. Which indicator works in the pH range
titration of NaOH and oxalic acid:-
8 – 9.8
(1) Methyl orange (2) Methyl red
(1) Phenolphthalein(2) Methyl orange
(3) Phenolphthalein (4) Starch
solution (3) Methyl red (4) Litmus

74 E
Chemistry For NEET By Prince Sir
15 . A basic - buffer will obey the equation change
pOH - pKb = 1 only under condition:- (3) Becomes 2 (4) Becomes 10
(1) [Conjugate acid] : [base] = 1
22. The pH of blood is maintained by CO2
: 10
and H2CO3 in the body and chemical
(2) [Conjugate acid] = [base] constituents of blood. This phenomenon
(3) [Conjugate acid] : [base] = 10 is called :-
: 1 (1) Colloidal (2) Buffer action
(4) N.O.T (3) Acidity (4) Salt balance

16 . For weak acid strong base titration, 23. Phenolphthalein is not a good indicator
the indicator used is :- for titrating
(1) Potassium di-chromate(2) Methyl (1) NaOH against oxalic acid
orange (2) NaOH against HCl
(3) Litmus ( 4 ) (3) NaOH against H2SO4
Phenolphthalein (4) Ferrous sulphate against KMnO4
17 . From the following in which titration 24. Which of the following solutions does
methyl orange is a best indicator :- not act as buffer :–
(1) CH3COOH + NaOH (1) H 3 PO 4 + NaH 2 PO 4
(2) H 2C 2 O 4 + NaOH (2) NaHCO 3 + H 2CO 3
(3) HCl + NaOH (3) NH4Cl + HCl
(4) CH3COOH + NH4OH (4) CH3COOH + CH3COONa
18. The total number of different kind 25. 50 mL of 2N acetic acid mixed with
of buffers obtained during the 10 mL of 1N sodium acetate solution
titration of H3PO4 with NaOH are will have an approximate pH of (Ka
:- = 10 –5 ) :–
(1) 3 (2) 1 (1) 4 (2) 5
(3) 2 (4) 0 (3) 6 (4) 7

19. The H+ ion concentration in 0.001 M 26. On addition of NaOH to CH 3COOH


acetic acid is 1.34 × 10–4 g ion L– s ol u ti on , 6 0 % of th e a ci d i s
1. The H+ ion concentration of 0.164
neutralised. If pKa of CH3COOH is
g of CH3COONa is added to a litre
of 0.001 M CH3COOH will be :- 4.7 then the pH of the resulting
solution is :-
(1) 9 × 10–6 (2) 18 × 10–6
(1) More than 4.7 but less than 5.0
(3) 4.5 × 10–6 (4) 5 × 10–6
(2) Less than 4.7 but more than 4.0
20. A certain acidic buffer solution (3) More than 5.0
contains equal concentration of X– (4) Remains unchanged
and HX. The Kb for X– is
–10
10 . The pH of the buffer is :- 27. 500 mL of 0.2 M acetic acid are added
t o
(1) 4 (2) 7
500 mL of 0.30 M sodium acetate
(3) 10 (4) 14 solution. If the dissociation
21. When 1.0 mL of dil. HCl acid is added constant of acetic acid is 1.5 × 10–
5
to 100 mL of a buffer solution of then pH of the resulting solution
pH 4.0. The pH of the solution is :-
(1) 5.0 (2) 9.0
(1) Becomes 7 (2) Does not
E 75
Chemistry For NEET By Prince Sir
(3) 3.0 (4) 4.0 to a litre of buffer solution, its
pH changes from 5.75 to 5.80. What
28. Half of the formic acid solution is is its buffer capacity :-
neutralised on addition of a KOH
(1) 0.4 (2) 0.05
solution to it. If
Ka (HCOOH) = 2 × 10–4 then pH of (3) – 0.05 (4) 2.5
the solution is : (log 2 = 0.3010)
33. Calculate the pH of a buffer prepared
(1) 3.6990 (2) 10.3010 by mixing 300 cc of 0.3 M NH3 and
(3) 3.85 (4) 4.3010 500 cc of 0.5 M NH4Cl. Kb for NH3
= 1.8 × 10 –5 :-
29. A solution contains 0.2M NH4OH and
(1) 8.1187 (2) 9.8117
0.2M NH4Cl. If 1.0 mL of 0.001 M
HCl is added to it. What will be the (3) 8.8117 (4) None of these

[OH ] of the resulting solution 34. What amount of sodium propanoate
[K b = 2 × 10 –5] :- should be added to one litre of an
(1) 2 × 10 –5 (2) 5 × 10 –10 aqueous solution containing 0.02 mole
of propanoic acid (Ka = 1.34 × 10–
(3) 2 × 10 –3 (4) None of these 5
at 25°C) to obtain a buffer solution
of pH 4.75 :-
30. Hunderson equation pH – pKa = 1
(1) 4.52 × 10–2 M(2) 3.52 × 10 –2
will be applicable to an acidic buffer M
when :-
(3) 2.52 × 10–2 M(4) 1.52 × 10 –2
(1) [Acid] = [Conjugate base] M
(2) [Acid] × 10 = [Conjugate base]
35. What will be the pH of the solution,
(3) [Acid] = [Conjugate base] × 10
if 0.01 moles of HCl is dissolved in
(4) None of these a buffer solution containing 0.02 moles
31. 0.05 M ammonium hydroxide solution of propanoic acid (Ka = 1.34 × 10–
5
is dissolved in 0.001 M ammonium ) and 0.0152 moles of salt, at 25°C
chloride solution. What will be the :
[log(0.173) = –0.76]
OH– ion concentration of this solution
(1) 3.11 (2) 4.11
: K b(NH 4OH) = 1.8 × 10 –5
(3) 5.11 (4) 6.11
(1) 3.0 × 10 –3 (2) 9.0 × 10 –4
(3) 9.0 × 10 –3 (4) 3.0 × 10 –4 36. Calculate the pH of a buffer solution
prepared by dissolving 30g of Na2CO3
32. When 0.02 moles of NaOH are added in 500 mL of an aqueous solution
containing 150 mL of 1M HCl. Ka for

 133  
HCO3– = 5.63 × 10-11  log    0 .0 5 
 150  

(1) 8.197 (2) 9.197

ANSWER KEY (3) 10.197 (4) 11.197 - 4


EXERCISE
37. Calculate the ratio of pH of a solution
Qu e. 1 2 3 4 5 6 7 8 containing
9 10 111mole12 of 13 14 +151
CH3COONa
An s. 1 2 3 4 1 4 3 3 mole
3 of 3 HCl 3 1
per litre 1and of
1 other
3
Qu e. 16 17 18 19 20 21 22 23 solution
24 25 containing
26 27 1 mole
28 CH COONa
29 3 30
+ 1mole of acetic acid per litre :-
An s. 4 3 1 1 1 2 2 4 3 1 1 1 1 1 2
(1) 1 : 1 (2) 2 : 1
Qu e. 31 32 33 34 35 36 37 38 39 40
(3) 1 : 2 (4) 2 : 3
An s. 2 1 3 4 2 3 3 4 1 1
M
76 38 . When 20 mL of NaOH are added to E
20
Chemistry For NEET By Prince Sir
EXERCISE-5 (PART-1) (B) presence of HCl increases the sulphide ion
concentration
1. The solubility product of a sparingle soluble salt AX2 (C) solubility product of group II sulphides is more
is 3.2 × 10–11. Its solubility (in mol/L) is than that of group IV sulphides
[CBSE AIPMT 2004] (D) sulphides of group IV cations are unstable in
–6 HCl
(A) 5.6 × 10 (B) 3.1 × 10–4
(C) 2 × 10–4 (D) 4 × 10–4 6. Which of the following pairs constitutes a buffer ?
[CBSE AIPMT 2006]
2. The rapid change of pH near the stoichiometric point
of an acid base titration is the basis of indicator (A) HNO2 and NaNO2 (B) NaOH and NaCl
detection. pH of the solution is related to ratio of the (C) HNO3 and NH\NO3 (D) HCl and KCl
concentrations of the conjugate acid (HIn) and bas
(In–) forms of the indicator given by the expression 7. The hydrogen ion concentration of a 10–8 M HCl
[CBSE AIPMT 2004] aqueous solution at 298 K (Kw = 10–14) is
[CBSE AIPMT 2006]
 I n 
(A) log  HIn   pK In  pH (A) 1.0 × 10–6 M (B) 1.0525 × 10–7 M
  (C) 9.525 × 10 M –8
(D) 1.0 × 10–8 M

 HIn  8. Calculate the pOH of a solution at 25°C that contains


(B) log     pK In  pH
 In  1 × 10–10 M of hydronium ion. [CBSE AIPMT 2007]
(A) 7.00 (B) 4.00
 HIn  (C) 9.00 (D) 1.00
(C) log     pH  pK I n
 In 
9. A weak acid, HA, has a Ka of 1.00 × 10–5. If 0.100 mole

 In  of this acid is dissolved in one litre of water, the
(D) log  HIn   pH  pK I n precentage of acid dissociated at equilibrium is closest
 
to [CBSE AIPMT 2007]

3. At 25°C, the dissociation constant of a base, BOH is (A) 99.0 % (B) 1.00%
1.0 × 10–12. The concentration of hydroxyl ions in 0.01 (C) 99.9% (D) 0.100%
M aqueous solution of the base would be
10. Equal volumes of three acid solution of pH 3, 4 and 5
[CBSE AIPMT 2005]
are mixed in a vessel. What will be the H+ ion
(A) 2.0 × 10–6 mol L–1 (B) 1.0 × 10–5 mol L–1 concentration in the mixture? [CBSE AIPMT 2008]
(C) 1.0 × 10–6 mol L–1 (D) 1.0 × 10–7 mol L–1 (A) 1.11 × 10–4 M (B) 3.7 × 10–4 M
4. What if the correct relationship between the pH of (C) 3.7 × 10–3 M (D) 1.11 × 10–3 M
isomolar solutions of sodium oxide (pH1), sodium
11. The dissociation equilibrium of a gas AB2 can eb
sulphide (pH2), sodium selenide (pH3) and sodium
represented as
telluride (pH4) ? [CBSE AIPMT 2005]
2 AB2 (g)  2AB (g) + B2(g)
(A) pH1 > pH2  pH3 > pH4
The degreeof dissociation is x and is small compared
(B) pH1 < pH2 < pH3 < pH4
to 1. The expression relating the degree of
(C) pH1 < pH2 < pH3  pH4 dissociation (x) with equilibrium constant Kp and total
(D) pH1 > pH2 > pH3 > pH4 pressure is [CBSE AIPMT 2008]
(A) (2Kp / p) (B) (2Kp / p)1/3
5. H2S gas when passed through a solution of cation (C) (2Kp / p)1/2 (D) (Kp / p)
containing HCl presipitates the cations of second
group in qualitative analysis but not those belonging
to the fourth group. It is because
[CBSE AIPMT 2005]
(A) presence of HCl decreases the sulphide ion
concentration

E 77
Chemistry For NEET By Prince Sir
12. The values of Kp and Kp for the reactions (C) 8.73 (D) 9.08
1 2
X Y+Z ...(i)
20. Buffer solutions have constant acidity and alkalinity
and A  2B ...(ii) because [CBSE AIPMT 2012]
are in ratio of 9 : 1. If degree of dissociation of X and (A) these give unionised acid or base on reaction with
A be equal, then total pressure at equilibrium (i) and
added acid or alkali
(ii) are in the ratio [CBSE AIPMT 2008]
(B) acids and alkalies in these solutions are shielded
(A) 3 : 1 (B) 1 : 9
from attack by other ions
(C) 36 : 1 (D) 1 : 1
(C) they have larger excess of H+ or OH– ions
13. Which of the following molecules acts as a Lewis (D) they have fixed value of pH
acid? [CBSE AIPMT 2009]
21. Equimolar solutions of the following substances were
(A) (CH3)3B (B) (CH3)2O
prepared separately. Which one of these will record
(C) (CH3)3P (D) (CH3)3N the highest pH value? [CBSE AIPMT 2012]
(A) BaCl2 (B) AlCl3
14. The ionisation constant of ammonium hydroxide is
1.77 × 10–5 at 298 K. Hydrolysis constant of ammonium (C) LiCl (D) BeCl2
chloride is [CBSE AIPMT 2009]
22. pH of a saturated solution of Ba(OH)2 is 12. The value
(A) 5.65 × 10–10 (B) 6.50 × 10–12
of solubility product Ksp of Ba(OH)2 is
(C) 5.65 × 10–13 (D) 5.65 × 10–12
[CBSE AIPMT 2012]
–7
15. What is the [OH–] in the final solution prepared by (A) 3.3 × 10 (B) 5.0 × 10–7
mixing 20.0 mL of 0.050 M HCl with 30.0 mL of 0.10 M (C) 4.0 × 10–6 (D) 5.0 × 10–6
Ba(OH)2 ? [CBSE AIPMT 2009]
23. Which of the following is electron deficient?
(A) 0.10 M (B) 0.40 M
(C) 0.0050 M (D) 0.12 M [NEET 2013]
(A) (CH3)2 (B) (SiH3)2
16. In a buffer solution containing gqual concentration (C) (BH3)2 (D) PH3
of B– and H B, the Kb for B– is 10–10. The pH of buffer
solution is [CBSE AIPMT 2010] 24. Which of these is least likely to act as a Lewis base ?
(A) 10 (C) 7 [NEET 2013]
(C) 6 (D) 4 (A) CO (B) F –

3
(C) BF (D) PF3
17. What is [H+] in mol/L of a solution that is 0.20 M in
CH3COONa and 0.10 M in CH3COOH ? 25. Which of the following salts will give highest pH in
(Ka for CH3COOH = 1.8 × 10–5) water? [CBSE AIPMT 2014]
[CBSE AIPMT 2010] (A) KCl (B) NaCL
–4 –5
(A) 3.5 × 10 (B) 1.1 × 10 (C) Na2CO3 (D) H2SO3
–5 –6
(C) 1.8 ×10 (D) 9.0 × 10
26. Which one of the following pairs of solution is not
18. If pH of a saturated solution of Ba(OH)2 is 12, the acidic buffer? [CBSE AIPMT 2015]
value of its Ksp is [CBSE AIPMT 2010] (A) HClO4 and NaClO4
–6 3 –7 3
(A) 4.00 × 10 M (B) 4.00 × 10 M (B) CH3COOH and CH3COONa
–7 3 –6 3
(C) 5.00 × 10 M (D) 5.00 × 10 M (C) H2CO3 and Na2CO3
(D) H3PO4 and Na3PO4
19. A buffer solution is prepared in which the
concentration of NH3 is 0.30 M and the concentration 27. What is the pH of the resulting solution when equal
of NH 4 is 0.20 M. If the equilibrium constant, Kb for volumes of 0.1 M NaOH and 0.01 M HCl are mixed?
NH3 equals 1.8 × 10–5, what is the pH of this solution? [CBSE AIPMT 2015]
(log 2.7 = 0.43) [CBSE AIPMT 2011] (A) 12.65 (B) 2.0
(A) 9.43 (B) 11.72 (C) 7.0 (D) 1.04

78 E
Chemistry For NEET By Prince Sir
28. The Ksp of Ag 2CrO 4, AgCl AgBr and AgI are 34. The solubility of BaSO4 in water is 2.42 × 10–3 gL–1 at
respectively, 1.1 × 10–12, 1.8 × 10–10, 5.0 × 10–13, 8.3 × 298 K. The value of its solubility product (Ksp) will be
10–17. (Given molar mass of BaSO4 = 233 g mol–1 )
Which one of the following salts will precipitate last [NEET 2018]
if AgNO3 solution is added to the solution containing –14
(A) 1.08 × 10 mol L 2 –2
(B) 1.08 × 10–12 mol2 L–2
equal moles of NaCl, NaBr, NaI and Na2CrO4?
(C) 1.08 × 10–10 mol2 L–2 (D) 1.08 × 10–8 mol2 L–2
[CBSE AIPMT 2015]
(A) Agl (B) AgCl
(C) AgBr (D) Ag2CrO4

29. Which of the following fluoro-compounds is most


likely to behave as a Lewis base ?
[NEET 2016, Phase II]
(A) BF3 (B) PF3
(C) CF4 (D) SiF4

30. The solubility of AgCl(s) with solubility product 1.6


× 10–10 in 0.1 M NaCl solution would be
[NEET 2016, Phase II]
–5
(A) 1.26 × 10 M (B) 1.6 × 10–9 M
(C) 1.6 × 10–11 M (D) zero

31. The percentage of pyridine (C 5H5N) that forms


pyridinium ion (C5H5N+H) in a 0.10 M aqueous
pyridine solution (Kb for C5H5N = 1.7 × 10–9) is
[NEET 2016, Phase II]
(A) 0.0060% (B) 0.013%
(C) 0.77% (D) 1.6 %

32. My and NY3, two nearly insoluble salts, Have the


same Ksp values of 6.2 × 10–13 at room temperature.
Which statement would be true in regard to MY and
NY3? [NEET 2016, Phase I]
(A) The molar solubility of MY in water is less than
that of NY3.
(B) The salts My and NY3 are more soluble in 0.5M
KYthan in pure water
(C) The addition of the salt of KY to solution of My
and NY3 will have no effect on their solubilities
(D) The molar solubilities of MY and NY3 in water
are indentical.

33. Concentration of the Ag+ ions in a saturated solution


of Ag2C2O4 is 2.2 × 10–4 mol–1 soulbility proudct of
Ag2C2O4 is [NEET 2017]
(A) 2.42 × 10–8 (B) 2.66 × 10–12
(C) 4.5 × 10–11 (D) 5.3 × 10–12

E 79
Chemistry For NEET By Prince Sir
1. Which one of the follwoing in not a buffer solution ? 10. 40 mL of 0.1 M ammonia solution is mixed with 20 mL
(A) 0.8M H2S + 0.8M KHS of 0.1 M HCl. What is the pH of the mixture ?
(B) 2M C6H5NH2 + 2M C6H5NH3+Br– (pKb of ammonia solution is 4.74)
(C) 0.05M KClO4 + 0.05M HClO4 [2003] (A) 4.74 (B) 2.26
2. In which of the following acid-base titration, pH is (C) 9.26 (D) 5.00 [2006]
greater than 8 at equivalence point ? 11. The pH of the solution obtained on neutralisation of
(A) Acetic acid versus ammonia 40 mL 0.1 M NaOH with 40 mL 0.1 M CH3COOH is
(B) Acetic acid versus sodium hydroxide (A) 7 (B)8
(C) Hydrochloric acid versus ammonia
(C) 6 (D) 3 [2007]
(D) Hydrochloric acid versus sodium hydroxide
[2003] 12. During titration of acetic acid with aq. NaOH solution,
the neutralisation graph has a vertical line. This line
3. Dimethyl glyoxime gives a red precipitate with Ni2+,
indicates
which is used for its detection. To get this precipitate
readily the best pH range is
(A) < 1 (B) 2 - 3
(C) 3 - 4 (D) 9 - 11 [2004] pH
4. The compound insoluble in water is
(A) mercurous nitrate
(B) mercuric nitrate V
(C) mercurous chloride
(D) mercurous perchlorate [2004] (A) alkaline nature of equivalence
(B) acidic nature of equivalence
5. For the equilibrium H2O(l)  H2O(g) at 1 atm and 298 K,
(C) neutral nature of equivalence
(A) standard free energy change is equal to zero (G°
(D) depends on experimental proceeding. [2007]
< 0)
(B) free energy change is less than zero (G < 0)
13. When the temperature of reaction increase then the
(C) standard free energy change is less than zero (G°
effect on pH value will
< 0)
(A) increase
(D) standard free energy chagne is greater than zero
(G° > 0) [2004]
(D) decrease
(C) first increase then decrease
6. What is the pH of 0.01 M glycine solution ? For glycine, (D) remains same [1995, 2007]
Ka1 = 4.5  10–3 and Ka2 = 1.7  10–10 at 298 K ?
(A) 3.0 (B) 10.0
(C) 7.06 (D) 7.2 [2004, 2010] 14. The dissociation equilibrium of a gas AB2 can be
represented as
7. Of the following which change will shift the reaction
towards the product ? 2AB2 (g ) ƒ 2AB (g )  B 2 (g)

I2(g) ƒ 2I(g) , H r (298 K)  150 kJ The degree of dissociation is x and is small compared
to 1. The expression relating the degree of
(A) Increase in concentration of I dissociation (x) with equilibrium constant Kp and total
(B) Decrease in concentration of I2 pressure p is
(C) Increase in temperature (A) (2Kp/p)1/2 (B) Kp/p
(D) Increase in total pressure [2004]
(C) 2Kp/p (D) (2Kp/p)1/3 [2008]
8. When 10 mL of 0.1 M acetic acid (pKa = 5.0) is titrated
against 10 mL of 0.1 M ammonia solution (pKb = 5.0), 15. The correct order of increasing [H3O+] in the following
the equivalence point occure at pH aqueous solution is
(A) 5.0 (B) 6.0 (A) 0.01 M H2S < 0.01 M H2SO4 < 0.01 M NaCl < 0.01
(C) 7.0 (D) 9.0 [2005] M NaNO2
(B) 0.01 M NaCl < 0.01 M M NaNO2 < 0.01 M H2S <
9. For reaction, 2NOCl(g)  2NO(g) + Cl2(g), KC at 427°C is 3 0.01 M H2SO4
 10–6 mol–1. The value of Kp is nearly (C) 0.01 M NaNO2 < 0.01 M NaCl < 0.01 M H2S < 0.01
(A) 7.5  10–5 (B) 2.5  10–5 M H2SO4
(C) 2.5  10–4 (D) 1.75  10–4 [2005] (D) 0.01 M H2S < 0.01 M NaNO2 < 0.01 M NaCl < 0.01
M H2SO4 [2008]

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16. pH of a 0.01 M solution (Ka = 6.6  10–4) 1 RT
(C) (D) [2012]
(A) 7.6 (B) 8 RT 2
(C) 2.6 (D) 5 [2009]
25. At 60° and 1 atm, N2O4 is 50% dissociated into NO2
17. The equilibrium constant for mutarotation -D Glucose then Kp is
 -D Glucose is 1.8. What percentage of a form remains (A) 1.33 atm (B) 2 atm
at equilibrium ?
(C) 2.67 atm (D) 3 atm [2012]
(A) 35.7 (B) 64.3
(C) 55.6 (D) 44.4 [2009]
26. What will be solubility product of AX3 ?
18. A vessel of one litre capacity containing 1 mole of SO3 (A) 27S4 (B) 4S3
is heated till a state of equilibrium is attained. 4
(C) 36S (D) 9S3 [2013]
2SO3(g)  2SO2(g) + O2(g)
At equilibrium, 0.6 moles of SO2 had formed. The value 27. The equilibrium constant for the reaction,
of equilibrium constant is
1 1
(A) 0.18 (B) 0.36 H 2(g )  I 2(g) ƒ HI(g) is K C .
2 2
(C) 0.45 (D) 0.68
Equilibrium constant for the reaction,
[2000, 2009, 2015]
2HI(g)  H2(g) + I2(g) will be
19. Ksp of CaSO4.5H2O is 9  10–6, find the volume for 1 g of (A) 1/Kc (B) 1/(Kc)2
CaSO4 (M.wt. = 136). (C) 2/Kc (D) 2/(Kc)2 [2014]
(A) 2.45 litre (B) 5.1 litre
(C) 55.6 (D) 3.2 litre [2011]
28. Kp for the reaction A  B is 4. If initially only A is
present then what will be the partial pressure of B
20. Which of the following is not a characteristic of after equilibrium ?
equilibrium ? (A) 1.2 (B) 0.8
(A) Rate is equal in both directions. (C) 0.6 (D) 1 [2016]
(B) Measurable quantities are constant at equilibrium.
(C) Equilibrium occurs in reversible condition. 29. At 25°C, the solubility product of Mg(OH)2 is
(D) Equilibrium occurs only in open vessel at constant 1.0 × 10–11. At which pH, will Mg 2+ ions start
temperatrue. [2011] precipitating in the form of Mg(OH)2 from a solution
of 0.001 M Mg2+ ions?
21. 25 mL, 0.2 M Ca(OH)2 is neutralised by 10 mL of 1 M (A) 9 (B) 10
HCl. then pH of resulting solution is (C) 11 (D) 8 [2017]
(A) 1.37 (B) 9
(C) 12 (D) 7 [2011] 30. When NH3(0.1 M) 50 ml mix with HCl (0.1 M) 10 ml
then what is pH of resultant solution (Pkb = 4.75 )
22. At equilibrium which is correct ? (A) 9.25 (B) 10
(A) G = 0 (B) S = 0 (C) 9.85 (D) 4.15 [2018]
(C) H = 0 (D) G° = 0 [2012]
31. When CH3COOCH3 + HCl is titrated with NaOH then
23. Which has the highest pH ? at neutral point the colour of phenopthalein becomes
(A) CH3COOK (B) Na2CO3 colourless from pink due to : [2018]
(C) NH4Cl (D) NaNO3 [2012] (A) due to formation of CH3OH
(B) due to formation of CH3COOH which act as a
Kp weak acid.
24. for following reaction will be (C) Phenophalein vaporizes.
Kc
(D) due to presence of HCl
1
CO(g)  O2(g )  CO 2(g) 32. 2ICl  I2 + Cl2 KC = 0.14
2
Initial concentration of ICl is 0.6 M then equilibrium
1 concentration of I2 is : [2018]
(A) RT (B)
RT (A) 0.37M (B) 0.128 M
(C) 0.224 M (D) 0.748 M

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33. Which of the following have maximum pH? base and a weak acid, methyl orange can be used as
(A) Black coffee (B) blood an indicator.
(C) Gastric juice (D) Saliva [2018] Reason : Methyl orange changes its colour in pH
range of 7 to 9. [2009]
ASSERTION AND REASON
In each of the following questions, two statement are 42. Assertion : Aqueous solution of CoCl2 is pink in
given one is assertion and the other is reason. Examine colour. It turns blue in presence of conc. HCl.
the statement carefully and mark the correct answer Reason : It is due to the formation of [CoCl4]2–
according to the instruction given below [2013]
(A) If both the assertion and reason are true and EXERCISE - 5 :
reason explains the assertion
PART - 1
(B) If both the assertion and reason are true but reason
1. C 2. D 3. D 4. D 5. A 6. A
does not explain the assertion
7. B 8. B 9. B 10. B 11. B 12. C
(C) If assertion is true but reason is false
13. A 14. A 15. A 16. D 17. D 18. D
(D) If assertion is false but reason in true
19. A 20. A 21. A 22. B 23. C 24. C
(E) Both assertion & reason are false
25. C 26. A 27. A 28. D 29. B 30. B
34. Assertion : Activity of an enzyme is pH dependent. 31. B 32. A 33. D 34. C
Reason : Change in pH affects the solubility of the
enzyme in water. [2003] PART - 2
1. D 2. B 3. D 4. C 5. C 6. C
35. Assertion : Addition of silver ions to a mixture of
7. C 8. C 9. D 10. C 11. B 12. A
aqueous sodium chloride and sodium bromide solution 13. B 14. D 15. C 16. C 17. A 18. D
will first precipitate AgBr rather than AgCl. 19. A 20. D 21. D 22. A 23. B 24. C
Reason : Ksp of AgCl < Ksp of AgBr. [2004] 25. B 26. A 27. B 28. B 29. B 30. C
31. b 32. B 33. B 34. B 35. C 36. D
36. Assertion : Sb2S3 is not soluble in yellow ammonium
37. D 38. C 39. A 40. D 41. D 42. A
sulphide.
Reason : The common ion effect due to S2– ions reduces
the solubility of Sb2S3. [2006]

37. Assertion : Mixture of CH3COOH and CH3COONH4 is


an example of acidic buffer.
Reason : Acidic buffer contains equimolar mixture of
weak acid and its salt with weak base.
[2007, 2014]

38. Assertion : The equilibrium constant is fixed and a


characteristic for any given chemical reaction at a
specified temperature.
Reason : The composition of the final equilibrium
mixture at a particular temperature depends upon the
starting amount of reactants. [2007, 2010]

39. Assertion : According to Le-Chatelier’s principle


addition of heat ot an equilibrium solid  liquid result in
decrease in the amount ot soild.
Reason : Reaction is endothermic, so on heating
forward reaction is favoured. [2008]

40. Assertion : Ice  Water, if pressure is applied water will


evaporate.
Reason : Increase of pressure pushes the equilibrium
towards the side in which number of gaseous molecule
increases. [2009]

41. Assertion : In an acid-base titration involving strong

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