Et

Acid Insights

Acid strength · pKa, Ka and conjugate bases

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CH3COOH

Ethanoic 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