CH3COOHEthanoic acid (acetic)
Vinegar — the reference weak acid of every syllabus
PKA4.76
KA1.74 × 10^-5
CONJUGATE BASECH3COO⁻
Moderately weak acidOrganic acid
Bar shows relative strength across the whole pKa scale (−25 to 50).
WHY THIS STRENGTHThe CH₃ group pushes electrons in, destabilising the ethanoate ion.
WHERE IT IS USEDVinegar, buffers, ester synthesis
MOST SEARCHED ACID STRENGTHS
STRENGTH LADDER — STRONGEST FIRST
RULES WORTH MEMORISING
- The lower the pKa, the stronger the acid — each unit is a factor of 10.
- Strong acids (HCl, HNO₃, H₂SO₄, HClO₄, HBr, HI) ionise completely; weak acids reach an equilibrium.
- Ka = 10^(−pKa); pH of a weak acid ≈ ½(pKa − log c).
- Electron-withdrawing groups (Cl, F, NO₂) strengthen an acid; alkyl groups weaken it.
- A stronger acid always has a weaker conjugate base.
- Carboxylic acids (pKa ≈ 4–5) ≫ phenols (≈10) ≫ alcohols (≈16).
- Down a group acidity rises (HF < HCl < HBr < HI); across a period it also rises (CH₄ < NH₃ < H₂O < HF).
75 acids and bases with measured pKa values