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Solubility product, written as KspK_{sp}, helps students predict how much of a sparingly soluble ionic compound dissolves in water. This cheat sheet focuses on worked example patterns, including writing KspK_{sp} expressions, finding molar solubility, and deciding whether a precipitate forms. Students need these tools for equilibrium problems where solids, ions, and saturated solutions appear together. The goal is to make each setup clear before doing the calculation. The key idea is that a slightly soluble salt reaches equilibrium between its solid form and its dissolved ions. For a salt AmBn(s)A_mB_n(s), the expression is Ksp=[An+]m[Bm]nK_{sp} = [A^{n+}]^m[B^{m-}]^n, and the solid is not included. The ion product QQ is compared with KspK_{sp} to predict precipitation: if Q>KspQ > K_{sp}, a precipitate forms. Common ions reduce solubility because they shift the dissolution equilibrium toward the solid.

Key Facts

  • For AmBn(s)mAn+(aq)+nBm(aq)A_mB_n(s) \rightleftharpoons mA^{n+}(aq) + nB^{m-}(aq), the solubility product is Ksp=[An+]m[Bm]nK_{sp} = [A^{n+}]^m[B^{m-}]^n.
  • Pure solids and liquids are not included in KspK_{sp} expressions because their activities are treated as constant.
  • For AgCl(s)Ag+(aq)+Cl(aq)AgCl(s) \rightleftharpoons Ag^+(aq) + Cl^-(aq), if the molar solubility is ss, then Ksp=s2K_{sp} = s^2.
  • For CaF2(s)Ca2+(aq)+2F(aq)CaF_2(s) \rightleftharpoons Ca^{2+}(aq) + 2F^-(aq), if the molar solubility is ss, then Ksp=s(2s)2=4s3K_{sp} = s(2s)^2 = 4s^3.
  • The ion product has the same form as KspK_{sp}, so for PbI2PbI_2, Q=[Pb2+][I]2Q = [Pb^{2+}][I^-]^2.
  • If Q<KspQ < K_{sp}, the solution is unsaturated and more solid can dissolve.
  • If Q=KspQ = K_{sp}, the solution is saturated and the system is at solubility equilibrium.
  • If Q>KspQ > K_{sp}, the solution is supersaturated and precipitation is predicted until QQ falls to KspK_{sp}.

Vocabulary

Solubility product
The equilibrium constant KspK_{sp} for the dissolving of a sparingly soluble ionic solid into its ions.
Molar solubility
The number of moles of a solute that dissolve per liter of solution, usually represented by ss in molL1\mathrm{mol\,L^{-1}}.
Saturated solution
A solution in which dissolved ions are in equilibrium with undissolved solid at a given temperature.
Ion product
The value QQ calculated from current ion concentrations using the same exponent pattern as the KspK_{sp} expression.
Common ion effect
The decrease in solubility caused by adding an ion already present in the dissolution equilibrium.
Precipitate
An insoluble or slightly soluble solid that forms when ion concentrations exceed the solubility limit.

Common Mistakes to Avoid

  • Including the solid in the KspK_{sp} expression is wrong because KspK_{sp} only uses dissolved ion concentrations, not the amount of solid present.
  • Forgetting coefficients become exponents is wrong because CaF2CaF_2 gives Ksp=[Ca2+][F]2K_{sp} = [Ca^{2+}][F^-]^2, not Ksp=[Ca2+][F]K_{sp} = [Ca^{2+}][F^-].
  • Using ss for every ion concentration without stoichiometry is wrong because CaF2CaF_2 produces [Ca2+]=s[Ca^{2+}] = s and [F]=2s[F^-] = 2s.
  • Comparing QQ and KspK_{sp} with different expressions is wrong because QQ must be built using the same ion powers as KspK_{sp}.
  • Ignoring a common ion is wrong because an initial concentration such as [Cl]=0.10M[Cl^-] = 0.10\,\mathrm{M} can greatly reduce the solubility of AgClAgCl.

Practice Questions

  1. 1 Write the KspK_{sp} expression for Ba3(PO4)2(s)3Ba2+(aq)+2PO43(aq)Ba_3(PO_4)_2(s) \rightleftharpoons 3Ba^{2+}(aq) + 2PO_4^{3-}(aq).
  2. 2 The molar solubility of AgClAgCl is 1.3×105M1.3 \times 10^{-5}\,\mathrm{M}. Calculate KspK_{sp} using Ksp=s2K_{sp} = s^2.
  3. 3 For CaF2CaF_2, Ksp=3.9×1011K_{sp} = 3.9 \times 10^{-11}. Find the molar solubility in pure water using Ksp=4s3K_{sp} = 4s^3.
  4. 4 A solution contains extra ClCl^- ions before AgClAgCl dissolves. Explain why the molar solubility of AgClAgCl is lower than in pure water.