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Study Guide: IB Chemistry How to Solve: IB Chemistry – Equilibrium (Kc, Kp, Le Chatelier, Acid-Base, Buffers)
Source: https://www.fatskills.com/ib-exams/chapter/ib-chemistry-how-to-solve-ib-chemistry-equilibrium-kc-kp-le-chatelier-acid-base-buffers

IB Chemistry How to Solve: IB Chemistry – Equilibrium (Kc, Kp, Le Chatelier, Acid-Base, Buffers)

By Fatskills Exam Guides Team — the exam nerds behind 28,500+ quizzes and 2.1M practice questions across 500+ global exams.

⏱️ ~5 min read

How to Solve: IB Chemistry – Equilibrium (Kc, Kp, Le Chatelier, Acid-Base, Buffers)

Complete Guide


Introduction

"Mastering equilibrium lets you predict how reactions shift under stress—like how your blood buffers pH when you sprint, or how industries maximise ammonia yield. On the IB exam, this topic is worth 15-20% of Paper 2, and missing one step can cost you 5+ marks. Let’s break it down so you never lose those marks again."


WHAT YOU NEED TO KNOW FIRST

  1. Dynamic equilibrium: Forward and reverse reactions occur at equal rates; concentrations remain constant.
  2. Stoichiometry: Balancing equations and mole ratios.
  3. Basic algebra: Rearranging equations and solving for unknowns.

KEY TERMS & FORMULAS

1. Equilibrium Constants (Kc and Kp)

Term Definition Formula Notes
Kc Equilibrium constant in terms of concentration (mol/dm³). Kc = [products] / [reactants] (each raised to stoichiometric coefficients) MEMORISE THIS
Kp Equilibrium constant in terms of partial pressures (atm or Pa). Kp = (P_products) / (P_reactants) MEMORISE THIS
Partial pressure Pressure exerted by one gas in a mixture. P_A = (moles of A / total moles) × total pressure Given on exam sheet
Reaction quotient (Q) Same as K, but for non-equilibrium conditions. Q = [products] / [reactants] Compare Q to K to predict shift

2. Le Chatelier’s Principle

Term Definition Effect on Equilibrium
Concentration Adding/removing reactants/products. Shifts to oppose the change.
Pressure Changing pressure (only affects gases). Shifts to side with fewer moles of gas if pressure ↑.
Temperature Changing temperature (exo/endothermic reactions). Shifts to absorb heat if temperature ↑.
Catalyst Speeds up both forward and reverse reactions equally. No shift in equilibrium position.

3. Acid-Base Equilibria

Term Definition Formula Notes
Ka Acid dissociation constant. Ka = [H⁺][A⁻] / [HA] MEMORISE THIS
Kb Base dissociation constant. Kb = [BH⁺][OH⁻] / [B] MEMORISE THIS
pH Measure of [H⁺] concentration. pH = -log[H⁺] Given on exam sheet
pKa Measure of acid strength. pKa = -log(Ka) Given on exam sheet
Kw Ionisation constant of water. Kw = [H⁺][OH⁻] = 1.0 × 10⁻¹⁴ at 25°C MEMORISE THIS

4. Buffers

Term Definition Formula Notes
Buffer Solution that resists pH change when small amounts of acid/base are added. Henderson-Hasselbalch: pH = pKa + log([A⁻]/[HA]) MEMORISE THIS

STEP-BY-STEP METHOD

1. Calculating Kc or Kp

Step 1: Write the balanced equation. Step 2: Write the K expression (products over reactants, raised to coefficients). Step 3: Substitute equilibrium concentrations (Kc) or partial pressures (Kp). Step 4: Solve for the unknown (K or a concentration/pressure). Step 5: Check units (Kc has no units; Kp uses atm or Pa).

2. Predicting Shifts (Le Chatelier’s Principle)

Step 1: Identify the stress (concentration, pressure, temperature). Step 2: Determine if the reaction is exo/endothermic (if temperature change). Step 3: Predict the shift (left/right) to oppose the change. Step 4: State the effect on yield (e.g., "more product formed").

3. Calculating pH, pKa, or Buffer pH

Step 1: Write the dissociation equation (e.g., HA ⇌ H⁺ + A⁻). Step 2: Write the Ka or Kb expression. Step 3: Substitute known values (initial concentrations, Ka/Kb). Step 4: Solve for [H⁺] or [OH⁻]. Step 5: Calculate pH = -log[H⁺] or use Henderson-Hasselbalch for buffers.


WORKED EXAMPLES

Example 1 – Basic (Kc Calculation)

Question: For the reaction N₂(g) + 3H₂(g) ⇌ 2NH₃(g), equilibrium concentrations are: [N₂] = 0.50 mol/dm³, [H₂] = 1.50 mol/dm³, [NH₃] = 0.20 mol/dm³. Calculate Kc.

Step 1: Write the Kc expression: Kc = [NH₃]² / ([N₂][H₂]³)

Step 2: Substitute values: Kc = (0.20)² / (0.50 × (1.50)³)

Step 3: Calculate: - (0.20)² = 0.04 - (1.50)³ = 3.375 - Denominator = 0.50 × 3.375 = 1.6875 - Kc = 0.04 / 1.6875 = 0.0237 (no units)

What we did and why: We used the Kc formula, substituted equilibrium concentrations, and solved algebraically. No shortcuts—always write the expression first!


Example 2 – Medium (Le Chatelier’s Principle)

Question: For the reaction 2SO₂(g) + O₂(g) ⇌ 2SO₃(g) ΔH = -198 kJ/mol, predict the effect of: a) Increasing pressure b) Increasing temperature c) Adding a catalyst

Step 1: Identify the stress: - a) Pressure ↑ - b) Temperature ↑ - c) Catalyst added

Step 2: Predict shifts: - a) Pressure ↑: Shifts to side with fewer moles of gas (right, 2 moles vs. 3 moles). - b) Temperature ↑: Shifts to absorb heat (left, since forward reaction is exothermic). - c) Catalyst: No shift (speeds up both directions equally).

What we did and why: We applied Le Chatelier’s Principle by analysing each stress separately. Always check if the reaction is exo/endothermic for temperature changes!


Example 3 – Exam-Style (Buffer pH Calculation)

Question: A buffer contains 0.10 mol/dm³ CH₃COOH (Ka = 1.8 × 10⁻⁵) and 0.20 mol/dm³ CH₃COO⁻. Calculate its pH.

Step 1: Write the Henderson-Hasselbalch equation: pH = pKa + log([A⁻]/[HA])

Step 2: Calculate pKa: pKa = -log(1.8 × 10⁻⁵) = 4.74

Step 3: Substitute values: pH = 4.74 + log(0.20 / 0.10)

Step 4: Solve: - log(2) = 0.30 - pH = 4.74 + 0.30 = 5.04

What we did and why: We used the Henderson-Hasselbalch equation because it’s a buffer. Never use Ka directly for buffers—this formula is faster!


COMMON MISTAKES

MISTAKE WHY IT HAPPENS CORRECT APPROACH
Forgetting coefficients in Kc/Kp Students write [products]/[reactants] without exponents. Always raise concentrations/pressures to their stoichiometric coefficients!
Ignoring units in Kp Students forget Kp uses atm or Pa, not mol/dm³. Check if the question gives pressures in atm or Pa.
Assuming catalysts shift equilibrium Students think catalysts favour products. Catalysts speed up both directions—no shift!
Using initial concentrations in Kc Students plug in initial values instead of equilibrium. Only use equilibrium concentrations in Kc!
Misapplying Le Chatelier for pressure Students forget pressure only affects gases. Count moles of gas on each side—solids/liquids don’t count!

EXAM TRAPS

TRAP HOW TO SPOT IT HOW TO AVOID IT
Q vs. K questions The question gives non-equilibrium concentrations. Calculate Q first, then compare to K to predict shift.
Units in Kp The question gives pressures in kPa but expects atm. Convert all pressures to the same unit (usually atm).
Temperature changes in Kc/Kp The question asks how Kc/Kp changes with temperature. Kc/Kp only changes with temperature—state if it increases or decreases.

1-MINUTE RECAP

"Here’s the night-before cheat sheet:
1.
Kc/Kp: Products over reactants, raised to coefficients. Only equilibrium values!
2.
Le Chatelier: Concentration? Oppose the change. Pressure? Fewer gas moles. Temperature? Absorb heat. Catalyst? No shift.
3.
Acid-base: Ka = [H⁺][A⁻]/[HA]. pH = -log[H⁺]. Buffers? Henderson-Hasselbalch: pH = pKa + log([A⁻]/[HA]).
4.
Common mistakes: Forgetting coefficients, using initial concentrations, ignoring units.
5.
Exam traps: Q vs. K, pressure units, temperature effects on K.

Write out one Kc and one buffer problem tonight. You’ve got this!