The Deceptive Nature of Ksp
Imagine you are handed two beakers, each containing a different sparingly soluble salt: A2X and MX. You are told that both salts share the exact same solubility product constant, Ksp=4.0×10−12. Your intuition might scream that because their Ksp values are identical, their molar solubilities must be identical too. But nature loves a good plot twist, and this is one of the classic traps in Ionic Equilibrium.
Analyzing the Setup
The A2X Salt
Let's break down the first salt, A2X. When it dissolves in water, it doesn't just split into two pieces; it shatters into three ions according to its stoichiometry:
If we define its molar solubility as S, then for every mole of A2X that dissolves, it yields 2S moles of A+ and S moles of X2−. The Law of Mass Action dictates that the solubility product is the product of these ion concentrations, raised to the power of their stoichiometric coefficients:
Substituting our terms, we get:
Solving for S, we divide by 4 to get S3=10−12. Taking the cube root is straightforward here: S=10−4 M.
The Master Equation
The MX Salt
Now, let's shift our focus to the second salt, MX. This is a simpler 1:1 salt. Its dissociation is straightforward:
Let's call its molar solubility S1. The concentration of both M+ and X− will simply be S1. The Ksp expression is much simpler:
Ksp=[M+][X−]=(S1)(S1)=S12
Equating this to our given Ksp:
Taking the square root gives us S1=2.0×10−6 M.
Final Calculation
The Grand Reveal
We now have the solubilities of both salts. S(A2X)=10−4 M and S(MX)=2.0×10−6 M. Notice how A2X is significantly more soluble than MX, despite having the same Ksp! This is because the S3 term in A2X allows it to reach the Ksp threshold at a much higher concentration than the S2 term in MX.
The question asks for the ratio of their molar solubilities:
S(MX)S(A2X)=2×10−610−4
To make the math visually cleaner, we can rewrite 10−4 as 100×10−6:
The ratio is exactly 50. This problem beautifully illustrates why you can never directly compare the Ksp values of salts with different stoichiometries to determine which is more soluble. You must always calculate their individual molar solubilities first!