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The Applications of solubility product

(i) In predicting formation of the precipitate

Case I : When Kip<Ksp, then solution is unsaturated in which more solute can be dissolved that is no precipitation.

Case II : When Kip=Ksp, then solution is saturated in which no more solute can be dissolved but no precipitate is formed.

Case III : When Kip>Ksp, then the solution is supersaturated and precipitation takes place.

When the ionic product exceeds solubility product, then the equilibrium shifts towards left-hand side that is increasing the concentration of undissociated molecules of the electrolyte. As solvent can hold the fixed amount of electrolyte at a specific temperature, the excess of the electrolyte is thrown out from the solutions as precipitate.

(ii) In predicting the solubility of the sparingly soluble salts knowing that the solubility product of a sparingly soluble salt at any specific temperature, we can predict its solubility.

(iii) Purification of common salt : HCl gas is circulated through the saturated solution of common salt. HCl and NaCl dissociate into their respective ions as,

1582_Applications of solubility product.png

The concentration of Cl- ions increases considerably in solution due to ionisation of HCl and due to common ion effect, dissociation of NaCl is decreased. Therefore, the ionic product [Na+][Cl-] exceeds the solubility product of NaCl and therefore pure NaCl precipitates out from the solution.

(iv) Salting out of the soap : From solution, soap is precipitated  when we add concentrated solution of NaCl.

  2343_Applications of solubility product1.png

Therefore, the ionic product [RCOO-] [Na+] exceeds solubility product of soap and thus, soap precipitates out from the solution.


(v) In the qualitative analysis: The separation and the identification of several basic radicals into different groups are based upon solubility product principle and the common ion effect.

(a) Precipitation of the radicals of group first (Pb+2, Ag+ , Hg+2) The group reagent is dilute HCl. [Ag+][Cl-]> Ksp for AgCl.

(b) Precipitation of group second radicals (Hg+2, Pb+2, Bi+3, Cu+2, Cd+2, As+3, Sb+3 and Sn+2) : The group reagent is H2S in presence of dilute HCl. [Pb2+][S-2]>Ksp for PbS.

(c) Precipitation of group third radicals (Fe+3, Al+3 and Cr+3) The group reagent is NH4OH in presence of NH4Cl. [Fe+3][OH-]> Ksp

 

(d) Precipitation of group fourth radicals (Co+2, Ni+2, Mn+2 and Zn+2) : The group reagent is H2S in presence of NH4OH.

[Co2+][S-2]>Ksp

(e) Precipitation of group fifth radicals (Ba+2, Sr+2, Ca+2)  The group reagent is ammonium carbonate in presence of NH4Cl and NH4OH.

[Ba2+][Co3-2]>Ksp

(vi) Calculation of remaining concentration after precipitation : Sometimes an ion remains after precipitation if it is in excess. The remaining concentration can be determined as follows,

Example 879_Applications of solubility product2.png;

In general 2438_Applications of solubility product3.png

% precipitation of ion = 873_Applications of solubility product4.png

(vii) Calculation of the simultaneous solubility : The solubility of two electrolytes possesing common ion; when they are dissolved in same solution, is known as simultaneous solubility.

Calculation of simultaneous solubility is divided into two cases.

Case I : When two electrolytes are nearly equally strong (having close solubility product).

e.g., 1441_Applications of solubility product5.png;

The charge balancing concept is applied hear.

Charge of Ag+           =   Charge of Br- +  Charge of SCN-

1435_Applications of solubility product6.png

Case II : When the solubility products of the two electrolytes are not close, which means they are not equally strong.

 e.g., 804_Applications of solubility product7.png    ;

Most of the fluoride ions come of the stronger electrolyte.

 

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