Question
Question: Silver chromate is sparingly soluble in aqueous solutions. The \({K_{sp}}\) of \(A{g_2}Cr{O_4}\) is ...
Silver chromate is sparingly soluble in aqueous solutions. The Ksp of Ag2CrO4 is 1.12×10−12 . What is the solubility (in mol/L) of silver chromate in 1.50 M potassium chromate aqueous solution? In 1.50 M silver nitrate aqueous solution and in pure water?
Solution
In this problem we are given the solubility constant Ksp . The value of Ksp is given as the product of the solubilities of the respective ions present in the salt, raised to their respective stoichiometries. The solutions given to us are silver chromate, potassium chromate, silver nitrate in water.
Complete answer:
We are given silver chromate having the chemical formula Ag2CrO4 . The Ksp is given as 1.12×10−12 .
1. The first solvent given to us is water, only silver chromate and water is present in the solution. Therefore, consider the solubilities of ions of silver chromate in water to be ‘s’. The dissociation can be given as:
Ag2CrO4 ⇌ 2Ag+ + CrO42−
T=0 | a | - | - |
---|---|---|---|
T=equilibrium | a−s | 2s | s |
The Ksp can be given as the product of the solubilities of products. Mathematically it can be shown as: Ksp=(2s)2(s)=1.12×10−12
Ksp=4s3=1.12×10−12
Therefore, s=341.12×10−12
s=0.65×10−4=6.5×10−5mol/L
This is the solubility of silver chromate in water.
2. The next solvent we are given is 1.50M potassium chromate. We can see that in both salts Chromate ion is common. In this question we are given that Ag2CrO4 and Potassium chromate, in here the common ion effect will come into play. The common ion in both the solutions is CrO42− . Hence the concentration of CrO42− will increase in the resultant solution.
The dissociation of 1.50 M potassium chromate can be given as: K2CrO4⇌2K++CrO42− . Therefore, the concentration of CrO42− will also be 1.50M. The dissociation of silver chromate can hence be given as
Ag2CrO4 ⇌ 2Ag+ + CrO42−
T=0 | a | - | - |
---|---|---|---|
T=equilibrium | a−s | 2s | s+1.50 |
The Ksp is given as 1.12×10−12 . Mathematically can be given as: : Ksp=(2s)2(s+1.50)=1.12×10−12
The value of s is very small compared to 1.50M
Ksp=(2s)2(1.50)=1.12×10−12
Ksp=4×s2×1.50=1.12×10−12
Ksp=6s2=1.12×10−12
Therefore, s=261.12×10−12=0.43×10−6mol/L
This is the solubility in potassium chromate.
3. The next solvent we are given is 1.50M silver nitrate. We can see that in both the salts silver ions are common. In this question we are given that Ag2CrO4 and silver nitrate, in here the common ion effect will come into play. The common ion in both the solutions is Ag+ . Hence the concentration of Ag+ will increase in the resultant solution.
The dissociation of 1.50 M potassium chromate can be given as: AgNO3⇌Ag++NO3−. Therefore, the concentration of Ag+ will also be 1.50M. The dissociation of silver chromate can hence be given as:
Ag2CrO4 ⇌ 2Ag+ + CrO42−
T=0 | a | - | - |
---|---|---|---|
T=equilibrium | a−s | 2s+1.50 | s |
The Ksp is given as 1.12×10−12 . Mathematically can be given as: : Ksp=(2s+1.50)2(s)=1.12×10−12
The value of s is very small compared to 1.50M
Ksp=(1.50)2×s=1.12×10−12
Ksp=2.25s=1.12×10−12
Therefore, s=2.251.12×10−12=0.5×10−12=5×10−13mol/L
This is the solubility in silver nitrate.
Note:
The order of solubilities in different solvents can be given as: water>potassium chromate>silver nitrate. More the value of Ksp more will be the solubility in that respective solvent. If we are given two or more solutions having at least one common ion, always the common ion effect will come into play, and an increase in the concentration of that common ion is observed. If concentration of one ion is increased, the system will try to decrease the concentration and the equilibrium will move forward.