Solubility ProductJEE Main

Ksp → molar solubility — interactive Chemistry simulation for IIT-JEE.

Concept

For a sparingly-soluble salt, the solubility product KspK_{sp} is the equilibrium constant for its dissolution. From KspK_{sp} you can predict the molar solubility ss — how many moles dissolve per litre before the solution is saturated.

Key formula

AxByxAy++yBx,Ksp=xxyysx+yA_xB_y \rightleftharpoons x\,A^{y+} + y\,B^{x-}, \qquad K_{sp} = x^x\,y^y\,s^{\,x+y}

Derivation

At saturation, dissolving ss mol/L gives [Ay+]=xs[A^{y+}] = x s and [Bx]=ys[B^{x-}] = y s.

Substituting into Ksp=[Ay+]x[Bx]yK_{sp} = [A^{y+}]^x[B^{x-}]^y gives Ksp=(xs)x(ys)y=xxyysx+yK_{sp} = (xs)^x(ys)^y = x^x y^y\,s^{x+y}, which you invert to solve for ss.

Scenarios to explore

  • Solubility Product — Ksp to molar solubility for 1:1, 1:2 and 1:3 salts.

Real-world applications

  • Predicting whether a precipitate forms (compare Qsp with Ksp).
  • Selective precipitation in qualitative analysis.
  • The common-ion effect lowering solubility.

JEE exam tips

  • AB: s = √Ksp. AB₂ or A₂B: s = ∛(Ksp/4). AB₃: s = ⁴√(Ksp/27).
  • Precipitate forms when the ionic product Qsp > Ksp.
  • Higher xˣyʸ ⇒ a more soluble salt for the same Ksp.

Common mistakes

  • Forgetting the xˣyʸ factor for non-1:1 salts (e.g. Ksp = 4s³ for AB₂).
  • Equating Ksp directly with solubility.
  • Ignoring that a common ion suppresses solubility.

Exam traps to avoid

  • Comparing solubilities across different salt types by Ksp alone is wrong — convert to s first.
  • Common-ion problems: the added ion's concentration dominates, not s.