Identify species as Brønsted–Lowry acids, bases, and/or conjugate acid–base pairs, based on proton transfer involving those species.
By definition, a Brønsted–Lowry acid is a proton donor and a Brønsted–Lowry base is a proton acceptor. Everything in Unit 8 rests on that pair of sentences.
Water plays a special role in aqueous solutions: its molecular structure allows it to both accept protons from and donate protons to dissolved species. A substance that can act as either an acid or a base is amphiprotic. Water, HCO₃⁻, HSO₄⁻, and H₂PO₄⁻ are the standard examples.
When an acid or base ionizes in water, the conjugate acid–base pairs can be identified and their relative strengths compared. A conjugate pair differs by exactly one H⁺ — and therefore by exactly one unit of charge.
HA + H₂O ⇌ A⁻ + H₃O⁺
acid base conjugate base conjugate acid
Every proton-transfer reaction has two conjugate pairs: here HA/A⁻ and H₃O⁺/H₂O.
The inverse-strength relationship. The stronger an acid, the weaker its conjugate base. HCl is a strong acid, so Cl⁻ is such a weak base that it is essentially inert in water. Acetic acid is weak, so acetate is a meaningfully basic species. Quantitatively this is Ka × Kb = Kw (see 8.3).
For the reaction HCO₃⁻(aq) + HF(aq) ⇌ H₂CO₃(aq) + F⁻(aq), identify the acid, base, and the two conjugate acid–base pairs. Then explain why HCO₃⁻ is described as amphiprotic.
HF is the acid — it donates a proton, becoming F⁻.
HCO₃⁻ is the base — it accepts that proton, becoming H₂CO₃.
Conjugate pairs:
HF / F⁻ (acid / conjugate base)
H₂CO₃ / HCO₃⁻ (conjugate acid / base)
Amphiprotic: HCO₃⁻ acts as a base here by accepting a proton to form H₂CO₃. But it can also act as an acid by donating its own proton:
HCO₃⁻ + OH⁻ → CO₃²⁻ + H₂O
Because it can both donate and accept a proton, HCO₃⁻ is amphiprotic — which is exactly why the carbonate/bicarbonate system buffers blood.