What it covers: Proton transfer — Bronsted-Lowry acids/bases, pH/pOH, weak acid/base equilibria, molecular structure and acid strength, titrations, and buffers.
Exam weight: About 11–15% of the AP Chemistry exam — the second-highest weighted unit.
The big question: How do molecular structure and equilibrium together determine the strength and behavior of acids and bases in solution?
Big Ideas covered: Structure & Properties (SAP), Chemical Effects (CE).
Key topics at a glance
Bronsted-Lowry Acids & Bases
Acid = proton donor. Base = proton acceptor. Conjugate pairs differ by exactly one H⁺.
Strong Acid/Base pH
Complete dissociation — pH calculated directly from initial concentration. No equilibrium needed.
Weak Acid/Base Equilibria
Partial dissociation — use Ka or Kb with an ICE table. Ka × Kb = Kw for a conjugate pair.
Molecular Structure & Strength
More O atoms on an oxoacid = stronger acid. Bond polarity and atomic size also matter.
Strong vs. weak is a calculation difference, not a different chemical concept. Strong = direct calculation; weak = equilibrium calculation.
Molecular structure predicts strength before you ever calculate a number. More electronegative pull (more O atoms, higher electronegativity) means a stronger acid.
A titration curve is a story about equilibrium shifting in real time. Every point on the curve corresponds to a specific Q vs. K relationship.
A buffer's best operating range is near its pKa. Buffer capacity is highest when [acid] ≈ [conjugate base], i.e., near the half-equivalence point.
This unit is equilibrium (Unit 7) with a more specific vocabulary. Every Ka/Kb problem is really just a Unit 7 ICE table problem in disguise.
Common exam traps
Don't use the strong-acid shortcut on a weak acid. Weak acids require an ICE table with Ka — you cannot just divide concentration directly into pH.
The equivalence point of a weak acid/strong base titration is NOT pH 7. It's basic, because the conjugate base of the weak acid hydrolyzes water.
pH = pKa happens at the half-equivalence point, not the equivalence point. Don't confuse these two landmarks on a titration curve.
A buffer doesn't prevent pH change entirely — it resists it. Add enough acid or base and the buffer will eventually be overwhelmed.
Don't forget that water itself contributes H₃O⁺ and OH⁻. This usually doesn't matter except for extremely dilute solutions or very weak acids/bases.