IB Chemistry R3.1 R3.1.2

Strong & Weak Acids/Bases

Dissociation extent, experimental distinction, and the ionic product of water Kw.

Reactivity 3.1 SL & HL ⏱️ ~5 min revision

Strong vs Weak: The Ionisation Concept

The strength of an acid or base refers to its extent of ionisation (dissociation) in aqueous solution. not its concentration.

Specification Comparison

Strong vs Weak Acids and Bases

Property Strong Acid / Base Weak Acid / Base
Dissociation100% complete (\(\rightarrow\))Partial equilibrium (\(\rightleftharpoons\))
[H⁺] or [OH⁻]Equal to initial concentration (monoprotic)Much less than initial concentration
Electrical ConductivityHigh (high mobile ion concentration)Low (low mobile ion concentration)
Reaction RateFast (with metals, carbonates)Slow (with same equimolar reagents)

IB Required Lists

Memorise these. Any acid/base not on this list should be treated as weak.

Core Memorisation

Required Strong Acids & Bases

Strong Acids (Must Memorise)
  • Hydrochloric acid: \(\text{HCl}\)
  • Nitric acid: \(\text{HNO}_3\)
  • Sulfuric acid: \(\text{H}_2\text{SO}_4\)
Strong Bases (Must Memorise)
  • Group 1 hydroxides: \(\text{LiOH}, \text{NaOH}, \text{KOH}\)
  • Group 2 soluble hydroxides: \(\text{Ba(OH)}_2\)

Exam Trap: Strength ≠ Concentration

Strength = proportion of molecules that ionise (100% vs partial).
Concentration = amount of solute per unit volume (mol dm⁻³).

It is entirely possible to have a dilute strong acid (e.g. 0.0001 M HCl) and a concentrated weak acid (e.g. 5.0 M CH₃COOH). A dilute strong acid can have a lower pH than a concentrated weak acid because it fully ionises.

The pH Scale

R3.1.2 Strong & Weak Acids/Bases - IB | ChemEasy 0 2 4 6 7 9 11 14 Acidic Neutral Alkaline pH = −log₁₀[H⁺]
Key Formulas

pH and Water Auto-ionisation Formulas

\[\text{pH} = -\log_{10}[\text{H}^+] \quad\Longleftrightarrow\quad [\text{H}^+] = 10^{-\text{pH}}\] \[K_{\text{w}} = [\text{H}^+][\text{OH}^-] = 1.00 \times 10^{-14} \text{ at } 298\text{ K}\] \[\text{pH} + \text{pOH} = 14.00 \text{ (at } 298\text{ K)}\]

Self-Ionisation of Water & Kw

Water is amphiprotic and undergoes auto-ionisation:

H₂O(l) ⇌ H⁺(aq) + OH⁻(aq)

The equilibrium constant for this is the ionic product of water:

Kw = [H⁺][OH⁻] = 1.00 × 10⁻¹⁴ at 25°C

In pure water: [H⁺] = [OH⁻] = 1.0 × 10⁻⁷ mol dm⁻³ → pH = 7.00

HLTemperature Dependence of Kw

Auto-ionisation of water is endothermic (ΔH > 0). By Le Chatelier's principle, increasing temperature shifts equilibrium to the right → more H⁺ and OH⁻ → Kw increases → pH of pure water decreases.

HL Extension

Temperature Dependence of Kw and Water Neutrality

The auto-ionisation of water (\(\text{H}_2\text{O} \rightleftharpoons \text{H}^+ + \text{OH}^-\)) is endothermic (\(\Delta H > 0\)).

  • As temperature rises, equilibrium shifts right → \(K_{\text{w}}\) increases → \([\text{H}^+]\) increases → pH decreases below 7.00.
  • However, water remains strictly neutral because \([\text{H}^+] = [\text{OH}^-]\) always holds for pure water!

HLKa, pKa, Kb, pKb

HL Extension

Acid/Base Dissociation Constants (Ka, Kb)

For weak acid \(\text{HA} \rightleftharpoons \text{H}^+ + \text{A}^-\) and weak base \(\text{B} + \text{H}_2\text{O} \rightleftharpoons \text{BH}^+ + \text{OH}^-\):

\[K_{\text{a}} = \frac{[\text{H}^+][\text{A}^-]}{[\text{HA}]}, \quad \text{p}K_{\text{a}} = -\log K_{\text{a}}\]

Higher \(K_{\text{a}}\) (lower \(\text{p}K_{\text{a}}\)) = stronger acid.

\[K_{\text{b}} = \frac{[\text{BH}^+][\text{OH}^-]}{[\text{B}]}, \quad \text{p}K_{\text{b}} = -\log K_{\text{b}}\]

For conjugate pair: \(K_{\text{a}} \times K_{\text{b}} = K_{\text{w}}\) and \(\text{p}K_{\text{a}} + \text{p}K_{\text{b}} = 14\).

The Conjugate Relationship

For any conjugate acid-base pair:

Ka × Kb = Kw     and     pKa + pKb = pKw = 14.00 (at 25°C)

This means: the stronger an acid, the weaker its conjugate base (and vice versa). A strong acid like HCl has a conjugate base (Cl⁻) so weak it doesn't act as a base in water.

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