Ionic Equilibrium
The plot of $\mathrm{pH}$-metric titration of weak base $\mathrm{NH}_{4} \mathrm{OH}$ vs strong acid HCl looks like :
Class XII students were asked to prepare one litre of buffer solution of $\mathrm{pH} \,8.26$ by their Chemistry teacher: The amount of ammonium chloride to be dissolved by the student in $0.2\, \mathrm{M}$ ammonia solution to make one litre of the buffer is :
(Given: $\mathrm{pK}_{\mathrm{b}}\left(\mathrm{NH}_{3}\right)=4.74$
Molar mass of $\mathrm{NH}_{3}=17 \mathrm{~g} \mathrm{~mol}^{-1}$
Molar mass of $\mathrm{NH}_{4} \mathrm{Cl}=53.5 \mathrm{~g} \mathrm{~mol}^{-1}$ )
${K_{{a_1}}}$, ${K_{{a_2}}}$ and ${K_{{a_3}}}$ are the respective ionization constants for the following reactions (a), (b) and (c).
(a) ${H_2}{C_2}{O_4} \mathbin{\lower.3ex\hbox{$\buildrel\textstyle\rightarrow\over {\smash{\leftarrow}\vphantom{_{\vbox to.5ex{\vss}}}}$}} {H^ + } + H{C_2}O_4^ - $
(b) $H{C_2}O_4^ - \mathbin{\lower.3ex\hbox{$\buildrel\textstyle\rightarrow\over {\smash{\leftarrow}\vphantom{_{\vbox to.5ex{\vss}}}}$}} {H^ + } + {C_2}O_4^{2 - }$
(c) ${H_2}{C_2}O_4^{} \mathbin{\lower.3ex\hbox{$\buildrel\textstyle\rightarrow\over {\smash{\leftarrow}\vphantom{_{\vbox to.5ex{\vss}}}}$}} 2{H^ + } + {C_2}O_4^{2 - }$
The relationship between ${K_{{a_1}}}$, ${K_{{a_2}}}$ and ${K_{{a_3}}}$ is given as :
$20 \mathrm{~mL}$ of $0.1\, \mathrm{M} \,\mathrm{NH}_{4} \mathrm{OH}$ is mixed with $40 \mathrm{~mL}$ of $0.05 \mathrm{M} \mathrm{HCl}$. The $\mathrm{pH}$ of the mixture is nearest to :
(Given : $\mathrm{K}_{\mathrm{b}}\left(\mathrm{NH}_{4} \mathrm{OH}\right)=1 \times 10^{-5}, \log 2=0.30, \log 3=0.48, \log 5=0.69, \log 7=0.84, \log 11= 1.04)$
The solubility of AgCl will be maximum in which of the following?
A student needs to prepare a buffer solution of propanoic acid and its sodium salt with pH 4. The ratio of ${{[C{H_3}C{H_2}CO{O^ - }]} \over {[C{H_3}C{H_2}COOH]}}$ required to make buffer is ___________.
Given : ${K_a}(C{H_3}C{H_2}COOH) = 1.3 \times {10^{ - 5}}$
The Ksp for bismuth sulphide (Bi2S3) is 1.08 $\times$ 10$-$73. The solubility of Bi2S3 in mol L$-$1 at 298 K is :
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 :
If the solubility product of PbS is 8 $\times$ 10$-$28, then the solubility of PbS in pure water at 298 K is x $\times$ 10$-$16 mol L$-$1. The value of x is __________. (Nearest Integer)
[Given : $\sqrt2$ = 1.41]
Explanation:
$\mathrm{S}=\sqrt{K_{s p}}=\sqrt{8 \times 10^{-28}}=2 \sqrt{2} \times 10^{-14}$
$=2.82 \times 10^{-14}$
$=282 \times 10^{-16}$
$ \therefore $ Ans. 282
$\mathrm{K}_{\mathrm{a}}$ for butyric acid $\left(\mathrm{C}_{3} \mathrm{H}_{7} \mathrm{COOH}\right)$ is $2 \times 10^{-5}$. The $\mathrm{pH}$ of $0.2 \,\mathrm{M}$ solution of butyric acid is __________ $\times 10^{-1}$. (Nearest integer)
[Given $\log 2=0.30$]
Explanation:
$\mathrm{pH}$ of $0.2 \mathrm{M}$ solution,
$ \mathrm{pH}=\frac{1}{2} \mathrm{pK}_{\mathrm{a}}-\frac{1}{2} \log \mathrm{C} $
$ \begin{aligned} &=\frac{1}{2}(4 \cdot 7) - \frac{1}{2} \log (0.2) \\\\ &=2.35+0.35=2.7 \end{aligned} $
$ \mathrm{pH}=27 \times 10^{-1} $
At $310 \mathrm{~K}$, the solubility of $\mathrm{CaF}_{2}$ in water is $2.34 \times 10^{-3} \mathrm{~g} / 100 \mathrm{~mL}$. The solubility product of $\mathrm{CaF}_{2}$ is ____________ $\times 10^{-8}(\mathrm{~mol} / \mathrm{L})^{3}$. (Give molar mass : $\mathrm{CaF}_{2}=78 \mathrm{~g} \mathrm{~mol}^{-1}$)
Explanation:
$ \begin{aligned} \mathrm{K}_{\mathrm{sp}} &=\mathrm{s}(2 \mathrm{~s})^{2} \\\\ &=4 \mathrm{~s}^{3} \end{aligned} $
Solubility $(\mathrm{s})=2.34 \times 10^{-3} \mathrm{~g} / 100 \mathrm{~mL}$
$=\frac{2 \cdot 34 \times 10^{-3} \times 10}{78}$ mole $/$ lit
$=3 \times 10^{-4} \mathrm{~mole} / \mathrm{lit}$
$\therefore \mathrm{K}_{\mathrm{sp}}=4 \times\left(3 \times 10^{-4}\right)^{3}$
$ \begin{aligned} &=108 \times 10^{-12} \\\\ &=0.0108 \times 10^{-8}(\mathrm{~mole} / \mathrm{lit})^{3} \end{aligned} $
$ \begin{aligned} & \therefore x \approx 0 \end{aligned} $
In the titration of $\mathrm{KMnO}_{4}$ and oxalic acid in acidic medium, the change in oxidation number of carbon at the end point is ___________.
Explanation:
During titration of oxalic acid by $\mathrm{KMnO}_{4}$, oxalic acid converts into $\mathrm{CO}_{2}$.
$\therefore$ Change in oxidation state of carbon $=1$
The solubility product of a sparingly soluble salt A2X3 is 1.1 $\times$ 10$-$23. If specific conductance of the solution is 3 $\times$ 10$-$5 S m$-$1, the limiting molar conductivity of the solution is $x \,\times$ 10$-$3 S m2 mol$-$1. The value of x is ___________.
Explanation:
$ \begin{aligned} &\mathrm{K}_{\mathrm{sp}}=(2 \mathrm{~s})^{2}(3 s)^{3}=1.1 \times 10^{-23} \\\\ &\mathrm{~S} \approx 10^{-5} \end{aligned} $
For sparingly soluble salts
$ \begin{aligned} \wedge_{m} &=\wedge_{m}^{0} \\\\ \wedge_{m} &=\frac{\mathrm{k}}{\mathrm{S} \times 10^{3}} \\\\ &=\frac{3 \times 10^{-5}}{10^{-5}} \times 10^{-3} \\\\ &=3 \times 10^{-3} ~ \mathrm{Sm}^{2} \mathrm{~mol}^{-1} \end{aligned} $
pH value of 0.001 M NaOH solution is ____________.
Explanation:
50 mL of 0.1 M CH3COOH is being titrated against 0.1 M NaOH. When 25 mL of NaOH has been added, the pH of the solution will be _____________ $\times$ 10$-$2. (Nearest integer)
(Given : pKa (CH3COOH) = 4.76)
log 2 = 0.30
log 3 = 0.48
log 5 = 0.69
log 7 = 0.84
log 11 = 1.04
Explanation:
CH3COOH + NaOH $\to$ CH3COONa + H2O
After adding 25 ml of NaOH volume of mixture = 50 + 25 = 75 ml
Initially,
Number of millimole of NaOH = 25 $\times$ 0.1 = 2.5 mm
Number of millimole of CH3COOH = 50 $\times$ 0.1 = 5 mm
After nutrilisation,
Millimole of NaOH = 0
Millimole of CH3COOH = 5 $-$ 2.5 = 2.5 mm
Millimole of CH3COONa = 2.5
After nutrilisation,
Concentration of CH3COOH = $[C{H_3}COOH] = {{5 - 2.5} \over {75}} = {1 \over {30}}$
Concentration of CH3COONa = $[C{H_3}COONa] = {{ 2.5} \over {75}} = {1 \over {30}}$
${P^H} = {P^{Ka}} + \log {{[C{H_3}COONa]} \over {[C{H_3}COOH]}}$
$ = 4.76 + \log {{{1 \over {30}}} \over {{1 \over {30}}}}$
$ = 4.76 + \log (1)$
$ = 4.76 + 0$
$ = 4.76$
$ = 4.76 \times {10^{ - 2}}$
Concentration of $\mathrm{H}_{2} \mathrm{SO}_{4}$ and $\mathrm{Na}_{2} \mathrm{SO}_{4}$ in a solution is $1 \mathrm{M}$ and $1.8 \times 10^{-2} \mathrm{M}$, respectively. Molar solubility of $\mathrm{PbSO}_{4}$ in the same solution is $\mathrm{X} \times 10^{-\mathrm{Y}} \mathrm{M}$ (expressed in scientific notation). The value of $Y$ is ________.
[Given: Solubility product of $\mathrm{PbSO}_{4}\left(K_{s p}\right)=1.6 \times 10^{-8}$. For $\mathrm{H}_{2} \mathrm{SO}_{4}, K_{a l}$ is very large and $\left.K_{a 2}=1.2 \times 10^{-2}\right]$
Explanation:
Conentration of $\mathrm{H}_2 \mathrm{SO}_4=1 \mathrm{M}$
Conentration of $\mathrm{Na}_{2} \mathrm{SO}_{4}$ = $1.8 \times 10^{-2} \mathrm{M}$
From the above two equations, we get
$ \left[\mathrm{H}^{+}\right]=1 \mathrm{M} \text { and }\left[\mathrm{SO}_4^{2-}\right]=1.8 \times 10^{-2} $
$ K_c=\frac{1.8 \times 10^{-2} \times 1}{1}=1.8 \times 10^{-2} $
and it is given that $\mathrm{K}_{a_2}\left(\mathrm{Q}_c\right)=1.2 \times 10^{-2} \mathrm{M}$
Since, $\mathrm{K}_{a_2}$ (i.e., $\mathrm{Q}_c$ ) $<\mathrm{K}_c$
$\therefore$ Rather than dissociation of $\mathrm{HSO}_4^{-}$into $\mathrm{H}^{+}$and $\mathrm{SO}_4^{2-}$ ions, association between already present $\mathrm{H}^{+}$and $\mathrm{SO}_4^{2-}$ will take place.
Assuming ' $x$ ' mol/L of $\mathrm{SO}_4^{2-}$ and $\mathrm{H}^{+}$combines to form $\mathrm{HSO}_4^{-}$
$\begin{aligned} & \mathrm{K}_{a 2}=\frac{\left[\mathrm{H}^{+}\right]\left[\mathrm{SO}_4^{2-}\right]}{\left[\mathrm{HSO}_4^{-}\right]} \\\\ & 1.2 \times 10^{-2}=\frac{(1-x)\left(1.8 \times 10^{-2}-x\right)}{(1+x)} \\\\ & \because x<<1, \text { so }(1+x) \approx 1 \text { and }(1-x) \approx 1 \\\\ & 1.2 \times 10^{-2}=1.8 \times 10^{-2}-x \\\\ & x=\left(1.8 \times 10^{-2}\right)-\left(1.2 \times 10^{-2}\right) \\\\ & x=0.6 \times 10^{-2} \mathrm{M} \\\\ & \text { So, }\left[\mathrm{SO}_4^{2-}\right]=1.8 \times 10^{-2}-x \\\\ & {\left[\mathrm{SO}_4^{2-}\right] }=\left(1.8 \times 10^{-2}\right)-\left(0.6 \times 10^{-2}\right) \\\\ & {\left[\mathrm{SO}_4^{2-}\right] }=1.2 \times 10^{-2} \mathrm{M}\end{aligned}$
Given, $\quad \mathrm{K}_{s p}=1.6 \times 10^{-8}$
$ \therefore $ $y\left(1.2 \times 10^{-2}+y\right)=1.6 \times 10^{-8}$
Since, $y<<1$, So $1.2 \times 10^{-2}+y \approx 1.2 \times 10^{-2}$
So, $y \times 1.2 \times 10^{-2}=1.6 \times 10^{-8}$
$ \Rightarrow $ $y =\frac{1.6 \times 10^{-8}}{1.2 \times 10^{-2}}$
$ \Rightarrow $ $ y =1.33 \times 10^{-6} $
$ X \times 10^{-Y} \mathrm{M} =1.33 \times 10^{-6} \mathrm{M} $
So, $\mathrm{Y}=6$
Hence, the value of $Y$ is 6 .
A solution is prepared by mixing $0.01 \mathrm{~mol}$ each of $\mathrm{H}_{2} \mathrm{CO}_{3}, \mathrm{NaHCO}_{3}, \mathrm{Na}_{2} \mathrm{CO}_{3}$, and $\mathrm{NaOH}$ in $100 \mathrm{~mL}$ of water. $p \mathrm{H}$ of the resulting solution is _________.
[Given: $p \mathrm{~K}_{\mathrm{a} 1}$ and $p \mathrm{~K}_{\mathrm{a} 2}$ of $\mathrm{H}_{2} \mathrm{CO}_{3}$ are $6.37$ and 10.32, respectively; $\log 2=0.30$ ]
Explanation:
First acid base reaction between H2CO3 and NaOH takes place.

In the final solution, we have 0.01 mole Na2CO3 and 0.02 moles of NaHCO3.
Here, we have a buffer of NaHCO3 and Na2CO3.
$\therefore$ $pH = p{K_{{a_2}}} + \log {{[Salt]} \over {[Acid]}}$
$ = 10.32 + \log {{\left( {{{0.01} \over {0.1}}} \right)} \over {\left( {{{0.02} \over {0.1}}} \right)}}$
$ = 10.32 + \log {1 \over 2}$
$ = 10.32 - \log 2$
$ = 10.32 - 0.3$
$ = 10.02$
$\therefore$ $pH = 10.02$
Statement I : In the titration between strong acid and weak base methyl orange is suitable as an indicator.
Statement II : For titration of acetic acid with NaOH phenolphthalein is not a suitable indicator.
In the light of the above statements, choose the most appropriate answer from the options given below :
Select correct statement from the following :
Assertion A : During the boiling of water having temporary hardness, Mg(HCO3)2 is converted to MgCO3.
Reason R : The solubility product of Mg(OH)2 is greater than that of MgCO3.
In the light of the above statements, choose the most appropriate answer from the options given below :
[Given : The solubility product of Ca(OH)2 in water = 5.5 $\times$ 10$-$6]
(Given : The solubility product of Zn(OH)2 is 2 $\times$ 10$-$20)
Explanation:

Due to common-ion effect (presence of NaOH) the concentration of OH$-$ will be (2S + 0.1) $\approx$ 0.1
($\because$ 0.1 > > 2 S)
$\therefore$ Solubility of product,
${K_{sp}} = {(0.1)^2} \times S$
$2 \times {10^{ - 20}} = 0.01 \times S$
$ \Rightarrow S = {{2 \times {{10}^{ - 20}}} \over {0.01}} = 2 \times {10^{ - 18}}$
$\therefore$ x = 2
Explanation:

$[HCl] = {{20} \over {80}} = {1 \over 4}M = 2.5 \times {10^{ - 1}}M$
pH = $-$log 2.15 $\times$ 10-1 = 1 $-$ 0.3979 = 0.6021
pH = 6021 $\times$ 10-4
Explanation:

KSP = (3s)3 (2s)2
KSP = 108 s5 & s = (x/M)
KSP = 108${\left( {{x \over M}} \right)^5}$
given ${K_{sp}} = a{\left( {{x \over M}} \right)^5}$
comparing a = 108
Explanation:

$ \therefore $ Ksp = (s)2 = (8 $\times$ 10-4)2 = 64 $\times$ 10-8
In H2SO4 solution,

As S1 < < 0.01 so, S1 + 0.01 $ \simeq $ 0.01
$ \therefore $ Ksp = [Cd+2] [So$_4^{ - 2}$]
$ \Rightarrow $ 64 $\times$ 10-8 = S1 $\times$ 0.01
$ \Rightarrow $ S1 = 64 $\times$ 10-6
Explanation:
${pH} = {p{ka}} + \log {{[C{H_3}COONa]} \over {[C{H_3}COOH]}}$
$ \Rightarrow 5.74 = 4.74 + \log {{[C{H_3}COONa]} \over {[C{H_3}COOH]}}$
$ \Rightarrow 1 = \log {{[C{H_3}COONa]} \over {[C{H_3}COOH]}}$
$ \Rightarrow {{[C{H_3}COONa]} \over {[C{H_3}COOH]}} = 10$
$ \Rightarrow [C{H_3}COONa] = 10 \times 1 = 10$
Explanation:
$ \therefore $ The contribution of H+ from 2nd dissociation of H2SO3 can be neglected.

$ \Rightarrow $ ${{c{\alpha ^2}} \over {1 - \alpha }} = 1.7 \times {10^{ - 2}}$
$ \Rightarrow {{0.588{\alpha ^2}} \over {1 - \alpha }} = 1.7 \times {10^{ - 2}}$
$ \Rightarrow 58.8{\alpha ^2} = 1.7 - 1.7\alpha $
$ \Rightarrow 58.8{\alpha ^2} + 1.7\alpha - 1.7 = 0$
$\alpha = {{ - 1.7 + \sqrt {{{1.7}^2} + 4 \times 1.7 \times 58.8} } \over {2 \times 58.8}} = 0.156$
$[{H^ + }] = c\alpha = 0.092$
$pH = - \log [{H^ + }]$
$ = 1.036$
$ \approx 1$
Explanation:
$\matrix{ {{A_2}X} & \to & {2{A^ + }} & {{X^{2 - }}} \cr {} & {} & {2{S_1}} & {{S_1}} \cr } $
${K_{sp}} = 4S_1^3 = 4 \times {10^{ - 12}}$
S1 = 10$-$4
for MX
$\matrix{ {MX} & \to & {{M^ + }} & {{X^ - }} \cr {} & {} & {{S_2}} & {{S_2}} \cr } $
${K_{sp}} = S_2^2 = 4 \times {10^{ - 12}}$
S2 = 2 $\times$ 10$-$6
so, ${{{S_{{A_2}X}}} \over {{S_{MX}}}} = {{{{10}^{ - 4}}} \over {2 \times {{10}^{ - 6}}}} = 50$
Explanation:
pH = 7 + ${1 \over 2}$(pka $-$ pkb)
= 7 + ${1 \over 2}$ (5.23 $-$ 4.75)
= 7.24 $ \approx $ 7.
Explanation:
To calculate solubility of Pbl2 in 0.1 M solution of Pb(NO3)2,
(I) $\mathop {Pb{{(N{O_3})}_2}}\limits_{0. 1 M} \to \mathop {P{b^{2 + }}(aq)}\limits_{0.1 M} + \mathop {2NO_3^ - (aq)}\limits_{0. 2 M} $
(II) $Pb{I_2}(s)$ $\rightleftharpoons$ $\mathop {P{b^{2 + }}(aq)}\limits_S + \mathop {2{I^ - }(aq)}\limits_{2S} $
$\therefore$ [Pb2+] = S + 0.1 $\approx$ 0.1
$\because$ S < < 0.1
Now, Ksp = 8 $\times$ 10$-$9
[Pb2] [I$-$]2 = 8 $\times$ 10$-$9
0.1 $\times$ (2S)2 = 8 $\times$ 10$-$9
4S2 = 8 $\times$ 10$-$8 $\Rightarrow$ S = 141 $\times$ 10$-$6 M
$ \therefore $ x = 141
(A) 0.01 M HCl
(B) 0.01 M NaOH
(C) 0.01 M CH3COONa
(D) 0.01 M NaCl
Assertion (A): When Cu (II) and sulphide ions are mixed, they react together extremely quickly to give a solid.
Reason (R): The equilibrium constant of
Cu2+(aq) + S2–(aq) ⇌ CuS(s) is high because the solubility product is low.
$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 ?
Assertion : The pH of water increases with increase in temperature.
Reason : The dissociation of water into H+ and OH– is an exothermic reaction.
(Note : consider that an appropriate indicator is used)
[Assuming that neither kind of ion reacts with water]
Explanation:
| AB2 | ⇌ | A2+(aq) | + | 2B-(aq) |
|---|---|---|---|---|
| s | 2s |
Ksp = 4s3 = 3.2 × 10–11
$ \Rightarrow $ s3 = 8 × 10–12
$ \Rightarrow $ s = 2 × 10–4
(First dissociation constant of
H2CO3 = 4.0 $ \times $ 10–7; log 2 = 0.3; density
of the soft drink = 1 g mL–1) .
Explanation:
At 30 bar pressure mass of CO2 in 1 kg water = 44 gm
At 3 bar pressure mass of CO2 in 1 kg water = 4.4 gm
$ \therefore $ Moles of CO2 in 1 kg water = ${{4.4} \over {44}}$ = 0.1
| H2CO3 | ⇌ | H+ | + | HCO3- | |
|---|---|---|---|---|---|
| t = 0 | 0.1 | 0 | 0 | ||
| t = teq | 0.1(1 - $\alpha $) | 0.1$\alpha $ | 0.1$\alpha $ |
4.0 $ \times $ 10–7 = ${{0.1{\alpha ^2}} \over {1 - \alpha }}$
${1 - \alpha }$ $ \simeq $ 1
$ \Rightarrow $ 0.1${{\alpha ^2}}$ = 4 $ \times $ 10-7
$ \Rightarrow $ $\alpha $ = 2 $ \times $ 10-3
[H+] = 0.1$\alpha $ = 2 $ \times $ 10-4
$ \therefore $ pH = –[– 4 × log(2)] = 3.7 = 37 × 10–1
[Given : pKa of acetic acid = 4.75, molar mass of acetic of acid = 60 g/mol, log 3 = 0.4771] Neglect any changes in volume.
Explanation:
= ${3 \over {60}} \times 1000 \times {{20} \over {500}}$ = 2
milimole of HCl in 20 ml = 25 $ \times $ ${{20} \over {500}}$ = 1
milimole of NaOH 20 ml = ${1 \over 2} \times 5$ = 2.5
| NaOH | + | CH3COOH | $ \to $ | CH3COONa | + | H2O |
|---|---|---|---|---|---|---|
| 1.5 | 2 | 0 | 0 | |||
| 0 | 0.5 | 1.5 |
pH = pKa + log${{1.5} \over {0.5}}$
= 4.74 + log 3 = 5.22
Explanation:
$ \therefore $ In 10 L solution H2SO4 present = $9.8 \times {{10} \over {100}}$ gm
$ \Rightarrow $ In 10 L solution moles of H2SO4 present = ${{9.8} \over {98}} \times {{10} \over {100}}$
In one molecule of H2SO4 two H+ ion present.
$ \therefore $ In 10 L solution moles of H+ present = 2$ \times $${{9.8} \over {98}} \times {{10} \over {100}}$ = 0.02 moles
Also In 100 L solution NaOH present = 4 gm
$ \therefore $ In 40 L solution NaOH present = $4 \times {{40} \over {100}}$
$ \Rightarrow $ In 40 L solution moles of NaOH present = ${4 \over {40}} \times {{40} \over {100}}$
In one molecule of NaOH one OH- ion present.
$ \therefore $ In 40 L solution moles of OH- ion present = ${4 \over {40}} \times {{40} \over {100}}$ = 0.04 moles
As moles of OH- ion is more than H+ ion, so solution is basic.
$ \therefore $ Final Conc. of OH– = ${{0.04 - 0.02} \over {40 + 10}}$ = 4 $ \times $ 10-4
$ \therefore $ pOH = – log (4 ×10–4) = 3.4
pH = 14 – 3.4 = 10.6
$B + HA\buildrel {} \over \longrightarrow B{H^ + } + {A^ - }$
Explanation:
$pOH = p{K_b} + \log {{[B{H^ + }]} \over {[B]}}$
At half equivalence point :
[BH+] = [B] ($ \because $ pH = 11)
Therefore, pOH = pKb = 14 $-$ 11 = 3
$ \because $ pKb = 3.00
Use Ksp(ZnS) = 1.25 $ \times $ 10$-$22 and overall dissociation constant of
H2S, Knet = K1K2 = 1 $ \times $ 10-21.
Explanation:
${K_{sp}}(ZnS) = [Z{n^{2 + }}][{S^{2 - }}] = 1.25 \times {10^{ - 22}}$
$0.05 \times [{S^{2 - }}] = 1.25 \times {10^{ - 22}}$
$ \Rightarrow [{S^{2 - }}] = {{1.25 \times {{10}^{ - 22}}} \over {0.05}} \Rightarrow 25 \times {10^{ - 22}}M$
For H2S, $\mathop {{H_2}S}\limits_{(0.1M)} \buildrel {} \over \longrightarrow 2{H^ + } + \mathop {{S^{ - 2}}}\limits_{(25 \times {{10}^{ - 22}}M)} $
${K_{net}} = 1 \times {10^{ - 21}} = {{{{[{H^ + }]}^2}[{S^{2 - }}]} \over {[{H_2}S]}}$
$1 \times {10^{ - 21}} = {{{{[{H^ + }]}^2} \times 25 \times {{10}^{ - 22}}} \over {[0.1]}}$
${[{H^ + }]^2} = {1 \over {25}}$
$[{H^ + }] = {1 \over 5} = 0.2M$
0.1 M Formic acid (A),
0.1 M Acetic acid (B),
0.1 M Benzoic acid (C)





