Ch. 14
14.1 Brønsted-Lowry Acids and Bases
Acid: proton (H+) donor
Base: proton (H+) acceptor
Conjugate Acid-Base Pair: Acid becomes conjugate base after donating H+; base becomes conjugate acid after accepting H+
Amphiprotic: can act as both acid and base (e.g. H2O, HCO3−)
Acid ionization: HA + H2O → H3O+ + A−
Base ionization: B + H2O → BH+ + OH−
Autoionization of water: 2H2O → H3O+ + OH−
Kw = [H3O+][OH−] = 1.0 × 10⁻¹⁴ at 25 °C
14.2 pH and pOH
pH = -log[H3O+]
pOH = -log[OH−]
[H3O+][OH−] = 1.0 × 10⁻¹⁴
pH + pOH = 14 at 25 °C
Acidic: pH < 7, Neutral: pH = 7, Basic: pH > 7
14.3 Relative Strengths of Acids and Bases
Strong acid: complete ionization (Ka ≈ ∞)
Weak acid: partial ionization (Ka measurable)
Ka = [H3O+][A−]/[HA]
Kb = [BH+][OH−]/[B]
Ka × Kb = Kw
Stronger acid → weaker conjugate base
Binary acid strength: Increases down a group, across a period with increasing electronegativity
Oxyacid strength: Increases with electronegativity and oxidation number of central atom
14.4 Hydrolysis of Salts
Cation from weak base (e.g. NH4+): acidic solution
Anion from weak acid (e.g. CH3COO−): basic solution
Neutral ions: conjugates of strong acids/bases (e.g. Na+, Cl−)
Hydrated metal ions (e.g. Al3+): act as weak acids due to polarizing water
14.5 Polyprotic Acids
Monoprotic: 1 ionizable H+ (e.g. HCl)
Diprotic: 2 ionizable H+ (e.g. H2SO4, H2CO3)
Ionization happens stepwise: Ka1 > Ka2
14.6 Buffers
Buffer = weak acid + conjugate base or weak base + conjugate acid
Resists pH change upon small additions of acid/base
Henderson-Hasselbalch equation:
pH = pKa + log([A−]/[HA])
Best buffer: when [A−] ≈ [HA] (pH ≈ pKa)
Buffers are effective within ±1 pH unit of pKa
14.7 Acid-Base Titrations
Titration curve: pH vs. volume of titrant
Equivalence point: moles acid = moles base
Strong acid + strong base: pH = 7 at equivalence
Weak acid + strong base: pH > 7 at equivalence
Indicators: weak acids/bases that change color with pH
Change color over range of pKa ± 1