Ethanoic acid to ethanol
1 step: reduction
Ethanoic acidCH₃COOHCarboxylic acid - Step 1
(i) LiAlH₄ (ii) H₃O⁺
EthanolCH₃CH₂OHAlcohol
Exam answer
- Step 1: Ethanoic acid to ethanol: (i) LiAlH₄ (ii) H₃O⁺.
Alternative routes (4)
- Ethanoic acid → Ethanoyl chloride → Ethanal → Ethanol
- Ethanoic acid to ethanoyl chloride: SOCl₂.
- Ethanoyl chloride to ethanal: H₂, Pd/BaSO₄.
- Ethanal to ethanol: NaBH₄.
- Ethanoic acid → Ethanamide → Ethanamine → Ethanol
- Ethanoic acid to ethanamide: NH₃, then heat.
- Ethanamide to ethanamine: (i) LiAlH₄ (ii) H₂O.
- Ethanamine to ethanol: NaNO₂ + HCl, 273 to 278 K.
- Ethanoic acid → Sodium ethanoate → Ethane → Chloroethane → Ethanol
- Ethanoic acid to sodium ethanoate: NaOH.
- Sodium ethanoate to ethane: electrolysis of the aqueous solution.
- Ethane to chloroethane: Cl₂, UV light.
- Chloroethane to ethanol: aq. NaOH (or aq. KOH).
- Ethanoic acid → Ethanoyl chloride → Ethanamide → Ethanamine → Ethanol
- Ethanoic acid to ethanoyl chloride: SOCl₂.
- Ethanoyl chloride to ethanamide: NH₃.
- Ethanamide to ethanamine: (i) LiAlH₄ (ii) H₂O.
- Ethanamine to ethanol: NaNO₂ + HCl, 273 to 278 K.
Reagent and reason, step by step
- Step 1: Ethanoic acid to ethanol: (i) LiAlH₄ (ii) H₃O⁺ Carboxylic acids are reduced to primary alcohols only by strong agents (LiAlH₄ or B₂H₆), not NaBH₄.
Points to note
- Step 1Carboxylic acids are reduced to primary alcohols only by strong agents (LiAlH₄ or B₂H₆), not NaBH₄.
Ethanoic acid to ethanol: quick answers
How many steps does it take to convert ethanoic acid to ethanol?
1 step: Ethanoic acid, then ethanol.
Which named reaction is used to convert ethanoic acid to ethanol?
None of the steps has a name. They are reduction, so write the reagent and the condition for each step.
What is the reagent for step 1 of ethanoic acid to ethanol?
Ethanoic acid to ethanol: (i) LiAlH₄ (ii) H₃O⁺. Carboxylic acids are reduced to primary alcohols only by strong agents (LiAlH₄ or B₂H₆), not NaBH₄.