Brønsted–Lowry acids and bases

Section: 7 Equilibria  |  Syllabus: Cambridge AS Level Chemistry (9701)

Common Acids and Alkalis

NameFormulaStrong or Weak?
Hydrochloric acidHClStrong acid
Sulfuric acidH₂SO₄Strong acid
Nitric acidHNO₃Strong acid
Ethanoic acidCH₃COOHWeak acid
Sodium hydroxideNaOHStrong base (alkali)
Potassium hydroxideKOHStrong base (alkali)
AmmoniaNH₃Weak base

The Brønsted–Lowry Theory

Brønsted–Lowry Acid A proton (H⁺) donor - a species that can donate a hydrogen ion to another species. Brønsted–Lowry Base A proton (H⁺) acceptor - a species that can accept a hydrogen ion from another species.

When an acid donates a proton it becomes its conjugate base. When a base accepts a proton it becomes its conjugate acid. These form conjugate acid–base pairs.

Fig 7.7 - Conjugate Acid–Base Pairs

Diagram: The equation HCl + H₂O ⇌ H₃O⁺ + Cl⁻ displayed with curved arrows. HCl is labelled "acid (proton donor)"; Cl⁻ is labelled "conjugate base of HCl". H₂O is labelled "base (proton acceptor)"; H₃O⁺ is labelled "conjugate acid of water". Two coloured brackets highlight conjugate pair 1 (HCl/Cl⁻) and conjugate pair 2 (H₂O/H₃O⁺).

Identifying Conjugate Pairs

Example 1: HCl(aq) + H₂O(l) ⇌ H₃O⁺(aq) + Cl⁻(aq)

Pair 1: HCl (acid) / Cl⁻ (conjugate base)

Pair 2: H₂O (base) / H₃O⁺ (conjugate acid)


Example 2: NH₃(aq) + H₂O(l) ⇌ NH₄⁺(aq) + OH⁻(aq)

Pair 1: NH₃ (base) / NH₄⁺ (conjugate acid)

Pair 2: H₂O (acid) / OH⁻ (conjugate base)

Amphoteric Species Water is amphoteric - it can act as both a Brønsted–Lowry acid (donating H⁺ to form OH⁻) and a Brønsted–Lowry base (accepting H⁺ to form H₃O⁺), depending on what it reacts with.

Strong and Weak Acids and Bases

Strong Acid Fully (completely) dissociates in aqueous solution - essentially an irreversible process:

HCl(aq) → H⁺(aq) + Cl⁻(aq)

A single arrow (→) is used, not a reversible arrow. Weak Acid Only partially dissociates in aqueous solution - an equilibrium is established between the undissociated acid and its ions. A reversible arrow (⇌) must be used:

CH₃COOH(aq) ⇌ CH₃COO⁻(aq) + H⁺(aq) Strong Base Fully dissociates in aqueous solution to produce OH⁻ ions:

NaOH(aq) → Na⁺(aq) + OH⁻(aq) Weak Base Only partially dissociates in aqueous solution:

NH₃(aq) + H₂O(l) ⇌ NH₄⁺(aq) + OH⁻(aq)

Comparing Strong and Weak Acids (same concentration)

PropertyStrong Acid (e.g. HCl)Weak Acid (e.g. CH₃COOH)
DissociationComplete (→)Partial (⇌)
pH at same concentrationLower (more H⁺ ions)Higher (fewer H⁺ ions)
Rate of reaction with MgFasterSlower
Electrical conductivityHigher (more ions present)Lower (fewer ions present)
Universal indicator colourBright redLighter red/orange
Fig 7.8 - Degree of Dissociation: Strong vs Weak Acid

Diagram: Two beakers side by side, both labelled 0.1 mol dm⁻³. Left beaker (HCl): all molecules shown fully dissociated as H⁺ and Cl⁻ ions - no HCl molecules remain. Right beaker (CH₃COOH): mostly intact CH₃COOH molecules with only a few H⁺ and CH₃COO⁻ ions present. pH meter readings displayed: ~1 for HCl and ~3 for CH₃COOH. Caption: "Same concentration - very different [H⁺]."

The pH Scale

Neutralisation and Salt Formation

Neutralisation The reaction between an acid and a base to form a salt and water. The net ionic equation for all neutralisations involving H⁺ and OH⁻ is:

H⁺(aq) + OH⁻(aq) → H₂O(l)

The spectator ions left in solution form the salt:

AcidBase/AlkaliSalt FormedEquation
HClNaOHSodium chloride (NaCl)HCl + NaOH → NaCl + H₂O
H₂SO₄KOHPotassium sulfate (K₂SO₄)H₂SO₄ + 2KOH → K₂SO₄ + 2H₂O
HNO₃NH₃Ammonium nitrate (NH₄NO₃)HNO₃ + NH₃ → NH₄NO₃
CH₃COOHNaOHSodium ethanoate (CH₃COONa)CH₃COOH + NaOH → CH₃COONa + H₂O
Link to Enthalpy The standard enthalpy of neutralisation for a strong acid + strong base is approximately −57 kJ mol⁻¹ per mole of water formed. For weak acid or weak base reactions, the value is less exothermic because energy is required to fully dissociate the weak acid or base.

pH Titration Curves

A pH titration curve plots pH (y-axis) against volume of base added from the burette (x-axis). The shape depends on the strength of the acid and base used.

Fig 7.9 - pH Curves for Four Titration Combinations

Diagram: Four separate pH vs volume graphs arranged in a 2×2 grid. (1) Strong acid + strong base: classic S-shaped curve with a sharp near-vertical section at the equivalence point at pH 7. (2) Weak acid + strong base: gradual rise initially (buffer region), then sharp section with equivalence point at pH 8–9. (3) Strong acid + weak base: sharp section with equivalence point at pH 5–6, then gradual rise. (4) Weak acid + weak base: no sharp section, equivalence point near pH 7. All graphs label the equivalence point and show the volume of base at the equivalence point.

Titration TypeEquivalence Point pHSharp Vertical Section?
Strong acid + strong basepH 7Yes - large and clear
Weak acid + strong basepH 8–9 (alkaline)Yes
Strong acid + weak basepH 5–6 (acidic)Yes
Weak acid + weak base~pH 7No - no sharp section
Why is the equivalence point above or below pH 7? When a weak acid is neutralised by a strong base, the resulting salt (e.g. CH₃COO⁻Na⁺) contains the conjugate base of the weak acid, which is itself a weak base - making the solution slightly alkaline. Conversely, when a weak base is neutralised by a strong acid, the salt is slightly acidic.

Choosing a Suitable Indicator

An indicator must change colour within the sharp vertical section of the titration curve. For weak acid–weak base titrations (no sharp section), no indicator is suitable - a pH meter must be used.

Fig 7.10 - pH Ranges of Common Indicators

Diagram: A horizontal pH scale from 0 to 14. Four coloured bars show the pH transition ranges of: methyl orange (red→orange, pH 3.1–4.4), litmus (red→blue, pH 5–8), phenolphthalein (colourless→pink, pH 8.2–10.0), and thymolphthalein (colourless→blue, pH 9.3–10.5). Vertical dashed lines at pH 5–6, 7, and 8–9 mark the equivalence points of the three titration types, showing which indicator's range overlaps with each equivalence point.

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