Let's review!
In this unit you learned what dynamic equilibrium is, wrote equilibrium constant expressions (K and Kp) and combined them, and used ICE tables to find K and equilibrium concentrations, including the small-K approximation. You compared Q with K to predict the direction of change, applied Le Châtelier's principle to changes in concentration, pressure, temperature and catalysts, and saw how chemists investigate shifts and measure K. In the extension you linked K to entropy and Gibbs free energy. Finally, you applied it all to the Haber and contact processes and to equilibria in the body and the environment.
Next comes Acid-Base and Solubility Equilibria, which uses every tool in this unit for Ka, Kb, Kw, Ksp, pH and buffers. This review has questions from every lesson. Try each one, then press Show answer.
How to use this review
Do two or three sections at a time with a scientific calculator. For each calculation, write the balanced equation, the K expression and an ICE table in mol/L before touching numbers. For each Le Châtelier question, name the stress, the shift and whether K changes. When you miss a question, write down why (wrong exponent? used moles? forgot to check 5 %? forgot that only temperature changes K?) and go back to that lesson. Finish with the 10-question quiz.
Check your understandingQuiz
2. The K expression for 2 A(g) + B(s) ⇌ C(g) is:
3. If K = 2.0 for X ⇌ Y, then K for 2 Y ⇌ 2 X is:
4. For A ⇌ B, [A]ᵢ = 1.0 mol/L and [B]ₑ = 0.20 mol/L. K is:
6. Which change increases K for an exothermic reaction?
7. For N₂(g) + O₂(g) ⇌ 2 NO(g), decreasing the volume:
8. The small-K approximation is valid when:
9. A catalyst added to the Haber process:
10. A reaction has ΔG° < 0 at 25 °C. Its K at 25 °C is: