Study Guides/Chemistry/Potassium Permanganate Oxidizes Ethanol To
Study Guide · Chemistry

What Does Potassium Permanganate Oxidize Ethanol To?

Potassium permanganate (KMnO₄) is a strong oxidizing agent. When it reacts with ethanol (C₂H₅OH), it oxidizes it first to ethanal (acetaldehyde, CH₃CHO) and then further to ethanoic acid (acetic acid, CH₃COOH). In acidic conditions, the oxidation goes all the way to acetic acid. This reaction is important in Class 10 and Class 12 Chemistry.

Question (Click to Flip)

What does potassium permanganate oxidize ethanol to?

Answer

Potassium permanganate (KMnO₄), especially in acidic medium, oxidizes ethanol (C₂H₅OH) to ethanoic acid (acetic acid, CH₃COOH). The oxidation occurs stepwise: ethanol → ethanal (acetaldehyde) → ethanoic acid.

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Key Facts

KMnO₄ oxidizes ethanol (C₂H₅OH) → ethanoic acid (acetic acid, CH₃COOH) in acidic medium.

Oxidation occurs in two steps: ethanol → ethanal → ethanoic acid.

KMnO₄ is purple/violet; it decolorizes on oxidizing ethanol (reduced to Mn²⁺).

K₂Cr₂O₇/H₂SO₄ also oxidizes ethanol to acetic acid.

PCC oxidizes primary alcohol only to aldehyde (stops at ethanal stage).

Tertiary alcohols are not oxidized by KMnO₄ under normal conditions.

Reaction: Ethanol Oxidized by KMnO₄

Step 1 — Ethanol → Ethanal (Acetaldehyde): C₂H₅OH → [O] → CH₃CHO (Primary alcohol → Aldehyde)

Step 2 — Ethanal → Ethanoic Acid (Acetic Acid): CH₃CHO → [O] → CH₃COOH (Aldehyde → Carboxylic acid)

Overall reaction: C₂H₅OH → [KMnO₄/H⁺] → CH₃COOH Ethanol → Acetic acid (Ethanoic acid)

So, potassium permanganate oxidizes ethanol to acetic acid (ethanoic acid).

Conditions for the Reaction

The product depends on the oxidizing conditions:

  1. Acidic KMnO₄ (KMnO₄/H₂SO₄ or KMnO₄/HCl): • Strongly oxidizing conditions • Primary alcohols → Carboxylic acids (all the way) • Ethanol → Ethanoic acid (acetic acid)

  2. Neutral/Alkaline KMnO₄: • Milder conditions • Can give complete oxidation to CO₂ and H₂O

  3. Other oxidizing agents: • K₂Cr₂O₇ / H₂SO₄ (acidified dichromate): also oxidizes ethanol to acetic acid • PCC (Pyridinium chlorochromate): oxidizes primary alcohol to aldehyde only (stops at ethanal)

Observation in the Reaction

Key observation: • KMnO₄ solution is purple/violet in colour • After oxidizing ethanol, the colour decolorizes (turns colourless) • This decolorization is evidence of oxidation • KMnO₄ is reduced from Mn⁷⁺ to Mn²⁺ (colourless manganese ions in acidic medium) or Mn⁴⁺ (brown MnO₂ in neutral medium)

This colour change is used as a test for the presence of reducing agents (alcohols, aldehydes).

General Oxidation of Alcohols

Type of alcohol | With strong oxidant (KMnO₄/H⁺) | With mild oxidant (PCC) Primary (e.g., ethanol) | Aldehyde → Carboxylic acid | Aldehyde only Secondary (e.g., propan-2-ol) | Ketone | Ketone Tertiary (e.g., tert-butanol) | No reaction (no α-H on correct side) | No reaction

Ethanol is a primary alcohol, so it is oxidized all the way to acetic acid by KMnO₄.

Questions and Answers

What does potassium permanganate oxidize ethanol to?+

Potassium permanganate (KMnO₄), especially in acidic medium, oxidizes ethanol (C₂H₅OH) to ethanoic acid (acetic acid, CH₃COOH). The oxidation occurs stepwise: ethanol → ethanal (acetaldehyde) → ethanoic acid.

What is the observation when KMnO₄ reacts with ethanol?+

KMnO₄ is purple/violet in colour. When it oxidizes ethanol, the purple colour decolorizes (becomes colourless in acidic medium) as Mn⁷⁺ is reduced to Mn²⁺. This colour change indicates a positive test for reducing agents.

What is the difference between KMnO₄ and PCC in oxidizing alcohols?+

KMnO₄ (strong oxidant): oxidizes primary alcohols all the way to carboxylic acids (ethanol → acetic acid). PCC (mild oxidant): oxidizes primary alcohols only to aldehydes (ethanol → ethanal/acetaldehyde) — stops at aldehyde stage.

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