To 100 ml of 0.1 M AgNO3 solution solid K2SO4 s added. The concentration of K2SO4 that shows precipitation is? (Ksp for Ag2SO4 = 6.4 * 10^-5 M)
(A) 0.1 M
(B) 6.4 * 10^-3 M
(C) 5.4 * 10^-7 M
(D) 6.4 * 10^-5 M
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2 Ag NO3 (aq) + K2 SO4 (aq) ==> Ag2 SO4 (s) + 2 K NO3 (aq)
Silver Sulfate is a non soluble precipitate. Ag NO3 is completely soluble.
Number of moles of AgNO3 in 0.1L of 0.1M solution: 0.1*0.1 = 0.01 moles.
Number of moles of K2SO4 reacting with 0.01 moles of AgNO3: 0.005 moles.
Ag2SO4 <==> 2 Ag⁺ + SO4⁻²
insoluble soluble
1 - x 2 x moles x moles
Ksp = Solubility product = [ Ag⁺ ]² [ SO4⁻² ] = 6.4 * 10⁻⁵
Precipitate forms if Ionic (concentration) product IP is more than Solubility product Ksp.
We have [Ag⁺] = 0.1 M. [ SO4⁻ ] = to find
IP = [Ag⁺]² [ SO₄ ⁻] = 0.1² [SO4⁻ ] = 0.01 [ SO4 ⁻ ]
IP > Ksp
So 0.01 [ SO4⁻ ] > 6.4 * 10⁻⁵
[ SO4 ⁻ ] > 6.4 * 10⁻³ M
In K2 SO4 there is only one Sulphate ion per molecule. So if concentration of Potassium Sulfate is more than this , then precipitate will form.
Silver Sulfate is a non soluble precipitate. Ag NO3 is completely soluble.
Number of moles of AgNO3 in 0.1L of 0.1M solution: 0.1*0.1 = 0.01 moles.
Number of moles of K2SO4 reacting with 0.01 moles of AgNO3: 0.005 moles.
Ag2SO4 <==> 2 Ag⁺ + SO4⁻²
insoluble soluble
1 - x 2 x moles x moles
Ksp = Solubility product = [ Ag⁺ ]² [ SO4⁻² ] = 6.4 * 10⁻⁵
Precipitate forms if Ionic (concentration) product IP is more than Solubility product Ksp.
We have [Ag⁺] = 0.1 M. [ SO4⁻ ] = to find
IP = [Ag⁺]² [ SO₄ ⁻] = 0.1² [SO4⁻ ] = 0.01 [ SO4 ⁻ ]
IP > Ksp
So 0.01 [ SO4⁻ ] > 6.4 * 10⁻⁵
[ SO4 ⁻ ] > 6.4 * 10⁻³ M
In K2 SO4 there is only one Sulphate ion per molecule. So if concentration of Potassium Sulfate is more than this , then precipitate will form.
kvnmurty:
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