Part of PC-06 — Equilibrium: Chemical & Ionic

Timeline/Sequence — Step-by-Step Processes

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Sequence A: How to Solve a Kp/Kc Problem

  1. Write the balanced chemical equation for the equilibrium.
  2. Identify which species are gaseous (for Kp) or aqueous/gaseous (for Kc); omit pure solids and liquids.
  3. Count Δn\Delta n = (moles of gaseous products) − (moles of gaseous reactants).
  4. Apply Kp = Kc(RT)^Δn\Delta n using R = 0.0821 L·atm/(mol·K) and T in Kelvin.
  5. Check units: Kp has units of (atm)^Δn\Delta n; confirm sign of Δn\Delta n matches the shift in K magnitude.

Sequence B: How to Predict Equilibrium Shift (Q Method)

  1. Write the equilibrium expression (same form as K).
  2. Substitute the CURRENT (non-equilibrium) concentrations to calculate Q.
  3. Compare Q with K: Q < K → forward; Q > K → backward; Q = K → equilibrium.
  4. Identify which direction reduces Q toward K.
  5. State which concentrations increase and decrease as a result.

Sequence C: Buffer Preparation

  1. Choose a weak acid with pKa within 1 unit of the target pH.
  2. Calculate required [salt]/[acid] ratio: log([salt]/[acid]) = pH − pKa.
  3. Dissolve calculated moles of weak acid and its conjugate salt in water.
  4. Verify using Henderson-Hasselbalch: pH = pKa + log([salt]/[acid]).
  5. Adjust with small amounts of strong acid or base if needed.

Sequence D: Solving Ksp and Solubility

  1. Write the dissolution equilibrium and its Ksp expression.
  2. Identify if a common ion is present in the solution.
  3. Set up ICE table: common ion provides initial concentration; s = solubility = increase.
  4. Apply simplifying assumption: s ≪ [common ion] if common ion is ≥ 100× more concentrated.
  5. Solve for s algebraically; verify the approximation holds.

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