Consider the slightly soluble compound MX for which
Ks is known.
For a solution of MX at equilibrium in the presence of undissolved solid, the product of concentrations in Q
s is equal to
Ks, the solubility constant for the compound
. For solutions that are not at equilibrium Q
s is NOT equal to
Ks. MX(s) M+(aq) + X–(aq) Qs = [M+][X–] | |
Thus
comparing the value of
Qs with
Ks for a solution containing the cation and anion of an sparingly soluble solid allows one to
establish- if the system is at equilibrium (Qs = Ks) AND
- if Qs is not equal to Ks to predict whether the amount of precipitate will be increased when equilibrium is reached
If the calculated
Qs is
- greater than Ks then the reaction that results in a lower concentration of the ions in solution (precipitation) is faster until Qs becomes equal to Ks (and more precipitate forms)
- less than Ks then the reaction that increases the concentration of the ions in solution is faster until Qs equals Ks. If there is precipiate present it will dissolve. If there is no precipitate present, no change will be observed.
Thus one can predict if mixing two solutions will give rise to a precipitate by calculating
Qs in the mixed solution. The
ion concentrations required are calculated by
- calculating the amount in moles of each substance mixed using n = cV (c and V are the concentration and volume of the solution containing that before mixing).
- dividing the result of 1 by the total volume in litres of the solution after mixing.