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S1.1 - Introduction to the particulate nature of matter S1.2 - The nuclear atom S1.3 - Electron configurations S1.4 - Counting particles by mass - The mole S1.5 - Ideal gases S2.1 - The ionic model S2.2 - The covalent model S2.3 - The metallic model S2.4 - From models to materials S3.1 - The periodic table - Classification of elements S3.2 - Functional groups - Classification of organic compounds R1.1 - Measuring enthalpy changes R1.2 - Energy cycles in reactions R1.3 - Energy from fuels R1.4 - Entropy and spontaneity AHL R2.1 - How much? The amount of chemical change R2.2 - How fast? The rate of chemical change R2.3 - How far? The extent of chemical change R3.1 - Proton transfer reactions R3.2 - Electron transfer reactions R3.3 - Electron sharing reactions R3.4 - Electron-pair sharing reactions

R2.3 - How far? The extent of chemical change

2.3.1 Dynamic Equilibrium 2.3.2 Equilibrium Constant, K 2.3.3 Understanding Ether Value of K 2.3.4 Le Chatelier Principle 2.3.5 Reaction Quotient, Q (AHL) 2.3.6 Solving Equilibrium Problems (AHL) 2.3.7 ∆G and the Equilibrium Constant, K (AHL)

Le Châtelier’s Principle

Specification Reference R2.3.4

Quick Notes:

  • Le Châtelier’s Principle: if a system at equilibrium is subjected to a change, the equilibrium shifts to oppose the change.
  • Factors affecting equilibrium position:
    • Concentration: Increasing reactants shifts equilibrium right and increasing products shifts equilibrium left.
    • Pressure (gases): Increasing pressure shifts equilibrium to the side with fewer gas molecules.
    • Temperature:
      • Endothermic (+ΔH) forward direction : Increasing temperature shifts equilibrium right.
      • Exothermic (−ΔH) forward direction: Increasing temperature shifts equilibrium left. .
    • Catalysts:Do not shift equilibrium, but increase the rate of both forward and reverse reactions equally.
  • K changes only with temperature, not with concentration or pressure.
  • Applies to homogeneous and heterogeneous equilibria.

Full Notes:

What Is Le Châtelier’s Principle?

Le Châtelier’s Principle states:

"If a system at equilibrium is subjected to a change, the position of equilibrium will shift to oppose that change."

This helps predict how a system reacts qualitatively to external changes.

Factors Affecting Equilibrium Position

Changing Concentration

Example Haber Process

Adding more N2 shifts equilibrium right, producing more NH3.

Changing Pressure (for Gaseous Equilibria)

Example Haber Process and Pressure

4 moles (N2 + 3H2) ⇌ 2 moles (NH3)

IB Chemistry Haber process diagram showing effect of pressure, with fewer moles of gas on the product side shifting equilibrium to the right at high pressure.

Higher pressure shifts equilibrium right, increasing NH3 yield.

Changing Temperature

Example Haber Process and Temperature

Forward reaction is exothermic (−ΔH).

IB Chemistry Haber process energy profile showing forward reaction as exothermic and reverse as endothermic.

Catalysts and Equilibrium

A catalyst speeds up both the forward and reverse reactions by providing an alternative route with a lower activation energy.

Heterogeneous Equilibria

Le Châtelier’s Principle also applies to equilibria involving different phases.

Example Gas–solution equilibrium

X(g) ⇌ X(aq)

Summary

Linked Course Question

Reactivity 2.2 — Linked Course Question

Why do catalysts have no effect on the value of K or on the equilibrium composition?

Catalysts speed up both the forward and reverse reactions equally, so they help the system reach equilibrium faster, but they do not shift the position of equilibrium. Since the equilibrium constant (K) depends only on temperature, and not on reaction speed, a catalyst has no effect on the value of K or the final equilibrium composition.