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Question

Calculate the solubility of AgCN in a buffer solution of pH=3.00 assuming no complex formation.
Given : Ksp(AgCN)=2.2×1016, Ka (HCN)=6.2×1010.
(Given 1.33×109=3.64×105)

A
5.9×102 M
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B
1.9×105 M
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C
3.9×108 M
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D
9.4×108 M
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Solution

The correct option is B 1.9×105 M
Let "s" be the solubility of Ag+ in the buffer solution.
On dissolution silver remains as Ag+ but CN ions are converted mostly to HCN due to fixed acidity of the buffer.
Ka=[H+][CN][HCN]Or,[HCN][CN]=[H+]Ka=1036.2×1010=1.6×106
As each CN ion hydrolyses to yield one HCN.
s=[Ag+]=[CN]+[HCN]
From the ratio of [HCN]/[CN] we see , [CN]<<[HCN]. So, s=[Ag+]=[HCN]
Thus from the equation (1) we have ,
[CN]=s1.6×106Ksp=[Ag+][CN]
2.2×1016=s×s1.6×106s=[Ag+]=1.87×105 M


Alternate solution :
Let "s" be the solubility of Ag+ in the buffer solution.
The equilibrium reaction of AgCN is given below:
AgCN(s)Ag+(aq)+CN(aq)..(1)
s sx
CN(aq)+H+(aq)1(Ka)HCNHCN(aq)(2)
s c 0
sx cx x
HCN is a weak acid. So, Ka will be very small. Hence, 1(Ka)HCN is very high i.e., equilibrium shifts in the forward direction
sx0sx
Adding equations (1) and (2) :
AgCN(s)+H+(aq)KspKaAg+(aq)+HCN(aq)
cs s sKspKa=s2cs2×10166×1010=s20.001s3.33×107=s20.001s(3.33×1010)(3.33×107)s=s2s2+(3.33×107)s(3.33×1010)=0s=(3.33×107)±(3.33×107)24×1×(3.33×1010)2×1s=(3.33×107)+(3.33×107)24×1×(3.33×1010)2×1s=(3.33×107)+1.33×1092s=(3.33×107)+3.64×1052s=1.9×105 M.

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