Ionic Equilibrium

NEET Chemistry · 99 questions · Page 9 of 10 · Click an option or "Show Solution" to reveal answer

Q81
Which of the following statement(s) is/are correct? (A) The pH\mathrm{pH} of 1×108 M HCl1 \times 10^{-8}~ \mathrm{M} ~\mathrm{HCl} solution is 8 . (B) The conjugate base of H2PO4\mathrm{H}_{2} \mathrm{PO}_{4}^{-} is HPO42\mathrm{HPO}_{4}^{2-}. (C) Kw\mathrm{K}_{\mathrm{w}} increases with increase in temperature. (D) When a solution of a weak monoprotic acid is titrated against a strong base at half neutralisation point, pH=12pKa\mathrm{pH}=\dfrac{1}{2} \mathrm{pK}_{\mathrm{a}} Choose the correct answer from the options given below:
A (A),(B),(C)(\mathrm{A}),(\mathrm{B}),(\mathrm{C})
B (B), (C)
C (B), (C), (D)
D (A), (D)
Correct Answer
Option B
Solution

(A) The pH\mathrm{pH} of 1×108 M HCl1 \times 10^{-8}~ \mathrm{M} ~\mathrm{HCl} solution is 8.

This statement is incorrect.

For a strong acid like HCl, the concentration of H+ ions will be the same as the concentration of the acid, i.e., 1×108 M1 \times 10^{-8}~\mathrm{M}.

The pH can be calculated using the formula: pH=log[H+]=log(1×108)=8\mathrm{pH} = -\log [\mathrm{H}^+] = -\log (1 \times 10^{-8}) = 8 However, because the concentration is so low, it approaches the range where water auto-ionization becomes significant.

In this case, the solution pH will be slightly higher than 7, but not exactly 8.

(B) The conjugate base of H2PO4\mathrm{H}_{2} \mathrm{PO}_{4}^{-} is HPO42\mathrm{HPO}_{4}^{2-}.

This statement is correct.

The conjugate base of an acid is formed when it loses one H+ ion: H2PO4HPO42+H+\mathrm{H}_{2} \mathrm{PO}_{4}^{-} \rightarrow \mathrm{HPO}_{4}^{2-} + \mathrm{H}^{+} (C) Kw\mathrm{K}_{\mathrm{w}} increases with an increase in temperature.

This statement is correct.

The ion product of water, Kw\mathrm{K}_{\mathrm{w}}, increases with increasing temperature.

This is because the auto-ionization of water is an endothermic process, meaning it absorbs heat: H2OH++OH\mathrm{H}_{2} \mathrm{O} \rightleftharpoons \mathrm{H}^{+} + \mathrm{OH}^{-} As the temperature increases, the equilibrium shifts towards the formation of more H+\mathrm{H}^{+} and OH\mathrm{OH}^{-} ions, leading to an increase in Kw\mathrm{K}_{\mathrm{w}}.

(D) When a solution of a weak monoprotic acid is titrated against a strong base at the half-neutralization point, pH=12pKa\mathrm{pH}=\dfrac{1}{2} \mathrm{pK}_{\mathrm{a}} This statement is incorrect.

At the half-neutralization point, the concentration of the weak acid ([HA]) is equal to the concentration of its conjugate base ([A-]).

According to the Henderson-Hasselbalch equation: pH=pKa+log[A][HA]\mathrm{pH} = \mathrm{pK}_{\mathrm{a}} + \log \dfrac{[\mathrm{A}^{-}]}{[\mathrm{HA}]} At the half-neutralization point, the ratio of [A-] to [HA] is 1, so the equation becomes: pH=pKa+log(1)=pKa\mathrm{pH} = \mathrm{pK}_{\mathrm{a}} + \log (1) = \mathrm{pK}_{\mathrm{a}} Therefore, the correct answer is: (B) and (C) are correct.

Q82
Three reactions involving H2PO4H_2PO_4^− are given below : (i) H3PO4 + H2O \to H3O+ + H2PO4H_2PO_4^− (ii) H2PO4H_2PO_4^− + H2O \to HPO42HPO_4^{2−} + H3O+ (iii) H2PO4H_2PO_4^− + OH- \toH3PO4 + O2- In which of the above does H2PO4H_2PO_4^− act as an acid?
A (ii) only
B (i) and (ii)
C (iii) only
D (i) only
Correct Answer
Option A
Solution

To determine in which reactions H2PO4 H_2PO_4^- acts as an acid, we need to understand the Bronsted-Lowry concept of acids and bases.

According to this concept, an acid is a substance that donates a proton (H⁺) to another substance, while a base is a substance that accepts a proton.

Let's analyze each reaction : 1.

H3PO4+H2OH3O++H2PO4 H_3PO_4 + H_2O \to H_3O^+ + H_2PO_4^- In this reaction, H3PO4 H_3PO_4 is donating a proton to H2O H_2O , forming H3O+ H_3O^+ and H2PO4 H_2PO_4^- . H2PO4 H_2PO_4^- is the product of this reaction and is not acting as an acid here.

2.

H2PO4+H2OHPO42+H3O+ H_2PO_4^- + H_2O \to HPO_4^{2−} + H_3O^+ In this reaction, H2PO4 H_2PO_4^- donates a proton to H2O H_2O , resulting in HPO42 HPO_4^{2−} and H3O+ H_3O^+ . H2PO4 H_2PO_4^- is acting as an acid in this reaction.

3.

H2PO4+OHH3PO4+O2 H_2PO_4^- + OH^- \to H_3PO_4 + O^{2-} This reaction is not correctly balanced and does not follow standard chemical reaction rules.

The product O2 O^{2-} is highly unlikely in aqueous solutions due to its reactivity.

A more correct reaction would be H2PO4+OHHPO42+H2O H_2PO_4^- + OH^- \to HPO_4^{2−} + H_2O .

In this corrected reaction, H2PO4 H_2PO_4^- is donating a proton to OH OH^- , which makes it an acid.

Given the information, the correct option is : Option A : (ii) only This is because in reaction (ii), H2PO4 H_2PO_4^- is clearly acting as an acid by donating a proton to water.

In reaction (i), H2PO4 H_2PO_4^- is not acting as an acid but rather is formed as a product.

Reaction (iii) as written is chemically incorrect, but even in a corrected form, it would show H2PO4 H_2PO_4^- acting as an acid.

Q83
Given below are two statements one is labelled as Assertion A and the other is labelled as Reason R : Assertion A : The amphoteric nature of water is explained by using Lewis acid/base concept. Reason R : Water acts as an acid with NH3 and as a base with H2S. In the light of the above statements choose the correct answer from the options given below :
A Both A and R are true and R is the correct explanation of A.
B Both A and R are true but R is NOT the correct explanation of A.
C A is true but R is false.
D A is false but R is true.
Correct Answer
Option D
Solution

The amphoteric nature of water is explained by using Bronsted-Lowry acid base concept

H2O (acid) +NH3OH+NH4+\underset{\text{ (acid) }}{\mathrm{H}_{2} \mathrm{O}}+\mathrm{NH}_{3} \rightleftharpoons \mathrm{OH}^{-}+\mathrm{NH}_{4}^{+}
H2O (base) +H2 SH3O++HS\underset{\text{ (base) }}{\mathrm{H}_{2} \mathrm{O}}+\mathrm{H}_{2} \mathrm{~S} \rightleftharpoons \mathrm{H}_{3} \mathrm{O}^{+}+\mathrm{HS}^{-}

Hence, A is false but R is true

Q84
The solubility product of Cr(OH)3 at 298 K is 6.0 × 10–31. The concentration of hydroxide ions in a saturated solution of Cr(OH)3 will be :
A (2.22 × 10–31)1/4
B (4.86 × 10–29)1/4
C (18 × 10–31)1/4
D (18 × 10–31)1/2
Correct Answer
Option C
Solution

Cr(OH)3 ⇌ Cr+3 + 3OH- S 3S Ksp = [Cr3+] [OH– ]3 \Rightarrow 6 × 10–31 = S × (3S)3 \Rightarrow 6 × 10–31 = 27 S4 S =

(627×1031)14{\left( {{6 \over {27}} \times {{10}^{31}}} \right)^{{1 \over 4}}}

As [OH–] = 3S =

3(627×1031)143{\left( {{6 \over {27}} \times {{10}^{31}}} \right)^{{1 \over 4}}}

= (18 × 10–31)1/4 M

Q85
Following four solutions are prepared by mixing different volumes of NaOH and HCl of different concentrations, pH of which one of them will be equal to 1 ?
A 100 mL M10{M \over {10}} HCl + 100 mL M10{M \over {10}} NaOH
B 75 mL M5{M \over {5}} HCl + 25 mL M5{M \over {5}} NaOH
C 60 mL M10{M \over {10}} HCl + 40 mL M10{M \over {10}} NaOH
D 55 mL M10{M \over {10}} HCl + 45 mL M10{M \over {10}} NaOH
Correct Answer
Option B
Solution

(a) 100 mL

M10{M \over {10}}

NaOH will nutalise 100 mL

M10{M \over {10}}

HCl, so number extra HCl will remain. This will be neutral solution

\therefore\,\,\,

pH = 7 (b) Here 25 mL

M5{M \over 5}

NaOH nutralise 25 mL

M5{M \over 5}

HCl

\therefore\,\,\,

Extra HCl = 75 - 25 = 50 mL Total volume = 75 + 25 = 100 mL

\therefore\,\,\,

Milimole of HCl =

505{{50} \over 5}

= 10

\therefore\,\,\,

Concentration of HCl =

10100{{10} \over {100}}

= 0.1

\therefore\,\,\,

pH = - log[H+] = - log(0.1) = 1 (c) HCl left = 60 - 40 = 20 mL

\therefore\,\,\,

milimole of HCl =

2010{{20} \over {10}}

= 2

\therefore\,\,\,

Concentration of HCl =

2100{2 \over {100}}

= 0.02 M

\therefore\,\,\,

pH = - log (0.02) = 1.69 (d) HCl left = 55 - 45 = 10 mL

\therefore\,\,\,

milimole of HCl =

1010{{10} \over {10}}

= 1

\therefore\,\,\,

Concentration of HCl =

1100{{1} \over {100}}

= 0.01 M

\therefore\,\,\,

pH = - log (0.01) = 2

Q86
If equal volumes of AB2A B_2 and XYX Y (both are salts) aqueous solutions are mixed, which of the following combination will give a precipitate of AY2\mathrm{AY}_2 at 300 K ? (Given Ksp(\mathrm{K}_{\mathrm{sp}}\left(\right. at 300 K ) for AY2=5.2×107\mathrm{AY}_2=5.2 \times 10^{-7} )
A 2.0×104MAB2,0.8×103MXY2.0 \times 10^{-4} \mathrm{M} \mathrm{AB}_2, 0.8 \times 10^{-3} \mathrm{M} \mathrm{XY}
B 2.0×102MAB2,2.0×102MXY2.0 \times 10^{-2} \mathrm{M} \mathrm{AB}_2, 2.0 \times 10^{-2} \mathrm{M} \mathrm{XY}
C 1.5×104MAB2,1.5×103MXY1.5 \times 10^{-4} \mathrm{M} \mathrm{AB}_2, 1.5 \times 10^{-3} \mathrm{M} \mathrm{XY}
D 3.6×103MAB2,5.0×104MXY3.6 \times 10^{-3} \mathrm{M} \mathrm{AB}_2, 5.0 \times 10^{-4} \mathrm{M} \mathrm{XY}
Correct Answer
Option B
Solution

When equal volumes of solutions are mixed, the molarity of each solution halves.

To determine if a precipitate will form, calculate the ionic product QSP\mathrm{Q}_{\mathrm{SP}} using the formula: QSP=[A2+][Y]2 \mathrm{Q}_{\mathrm{SP}} = \left[\mathrm{A}^{2+}\right]\left[\mathrm{Y}^{-}\right]^2 A precipitate of AY2\mathrm{AY}_2 will form if QSP>KSP\mathrm{Q}_{\mathrm{SP}} > \mathrm{K}_{\mathrm{SP}}, where KSP\mathrm{K}_{\mathrm{SP}} is given as 5.2×1075.2 \times 10^{-7}.

Option 1 Calculation: QSP=(1.8×103)(52×104)2=Calculated valueOption2Calculation: \mathrm{Q}_{\mathrm{SP}} = \left(1.8 \times 10^{-3}\right)\left(\dfrac{5}{2} \times 10^{-4}\right)^2 = \text{Calculated value} Option 2 Calculation: \mathrm{Q}_{\mathrm{SP}} = \left(10^{-4}\right)\left(0.4 \times 10^{-3}\right)^2 = \text{Calculated value} Option 3 Calculation: QSP=(102)(102)2=Calculated value>KSP \mathrm{Q}_{\mathrm{SP}} = \left(10^{-2}\right)\left(10^{-2}\right)^2 = \text{Calculated value} > \mathrm{K}_{\mathrm{SP}} Option 4 Calculation: QSP=(1.52×104)(1.52×103)2=Calculated valueFromthecalculations,thesolutioninOption3willformaprecipitatesincetheionicproduct \mathrm{Q}_{\mathrm{SP}} = \left(\dfrac{1.5}{2} \times 10^{-4}\right)\left(\dfrac{1.5}{2} \times 10^{-3}\right)^2 = \text{Calculated value} From the calculations, the solution in Option 3 will form a precipitate since the ionic product \mathrm{Q}_{\mathrm{SP}}isgreaterthanthesolubilityproduct is greater than the solubility product \mathrm{K}_{\mathrm{SP}}$.

Q87
The equilibrium Cr2O722CrO42\mathrm{Cr}_2 \mathrm{O}_7^{2-} \rightleftharpoons 2 \mathrm{CrO}_4^{2-} is shifted to the right in :
A a weakly acidic medium
B a basic medium
C a neutral medium
D an acidic medium
Correct Answer
Option B
Solution

The equilibrium

Cr2O722CrO42\mathrm{Cr}_2 \mathrm{O}_7^{2-} \rightleftharpoons 2 \mathrm{CrO}_4^{2-}

can be influenced by changes in the pH of the medium, according to Le Chatelier's principle.

This principle states that if a dynamic equilibrium is disturbed by changing the conditions, the position of equilibrium moves to counteract the change.

In this case:

Cr2O72\mathrm{Cr}_2 \mathrm{O}_7^{2-}

is dichromate, which exists more prominently in acidic conditions. On the other hand,

CrO42\mathrm{CrO}_4^{2-}

is chromate, which is favored in basic conditions.

When the medium is basic, hydrogen ion concentration decreases, leading to the formation of more chromate ions (

CrO42\mathrm{CrO}_4^{2-}

). Thus, in a basic medium, the reaction shifts to the right, resulting in the formation of

2CrO422 \mathrm{CrO}_4^{2-}

from

Cr2O72\mathrm{Cr}_2 \mathrm{O}_7^{2-}

. Therefore, the correct option is: Option B: a basic medium

Q88
50 mL of 0.2 M ammonia solution is treated with 25 mL of 0.2 M HCl. If pKb of ammonia solution is 4.75, the pH of the mixture will be :
A 3.75
B 4.75
C 8.25
D 9.25
Correct Answer
Option D
Solution

NH3 + HCl \to NH4Cl moles of HCl = 0.2 M × 25 × 10–3 L = 0.005 moles HCl (total consumed) moles of NH3 = 0.2 M × 50 × 10–3 L = 0.01 moles HCl excess NH3 = 0.01 – 0.005 = 0.005 moles From reaction, 1 mole ammonia = 1 mole NH4Cl \therefore 0.005 NH3 = 0.005 NH4Cl Total Volume = VHCl + VNH3 = 25 + 50 = 75 mL [NH3] = [NH4Cl] =

0.00575×103{{0.005} \over {75 \times {{10}^{ - 3}}}}

= 0.066 M pOH = pKb + log

[salt][base]{{\left[ {salt} \right]} \over {\left[ {base} \right]}}

= pKb + log

[NH4Cl][NH3]{{\left[ {N{H_4}Cl} \right]} \over {\left[ {N{H_3}} \right]}}

= 4.75 + log

[0.066][0.066]{{\left[ {0.066} \right]} \over {\left[ {0.066} \right]}}

\Rightarrow pOH = 4.75 \therefore pH = 14 – 4.75 = 9.25

Q89
The Ksp for the following dissociation is 1.6 × 10–5 PbCl2(s)Pb(aq)2++2Cl(aq)PbC{l_{2(s)}} \leftrightharpoons Pb_{(aq)}^{2 + } + 2Cl_{(aq)}^ - Which of the following choices is correct for a mixture of 300 mL 0.134 M Pb(NO3)2 and 100 mL 0.4 M NaCl ?
A Q > Ksp
B Not enough data provided
C Q < Ksp
D Q = Ksp
Correct Answer
Option A
Solution

[Pb2+] =

300×0.134400{{300 \times 0.134} \over {400}}

= 1.005 × 10–1 M [Cl-] =

100×0.4400{{100 \times 0.4} \over {400}}

= 10–1 M

PbCl2(s)Pb(aq)2++2Cl(aq)PbC{l_{2(s)}} \leftrightharpoons Pb_{(aq)}^{2 + } + 2Cl_{(aq)}^ -

Q = [Pb2+] × [Cl–]2 = 0.1005 × (0.1)2 = 1.005 × 10–3 Given Ksp = 1.6 × 10–5 \therefore Q > Ksp

Q90
What is the molar solubility of Al(OH)3 in 0.2 M NaOH solution ? Given that, solubility product of Al(OH)3 = 2.4 × 10–24 :
A 3 × 10–22
B 3 × 10–19
C 12 × 10–21
D 12 × 10–22
Correct Answer
Option A
Solution
Ksp={K_{sp}} =

[Al3+][OH-]3 \Rightarrow 2.4 × 10–24 = s(0.2)3 \Rightarrow s =

2.4×10248×103{{2.4 \times {{10}^{ - 24}}} \over {8 \times {{10}^{ - 3}}}}

\Rightarrow s = 3 × 10–22

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