Propanone on oxidation gives:

Correct answer: B. Formic acid + Acetic acid

  • A. Acetic acid
  • B. Formic acid + Acetic acid
  • C. Formic acid
  • D. Propionic acid

Explanation

The correct answer is B) Formic acid (HCOOH) and Acetic acid (CH3COOH). When propanone (acetone) is oxidized, it gives a mixture of formic acid and acetic acid as the products. The overall reaction can be represented as follows: CH3COCH3 + 2O2 → HCOOH + CH3COOH The oxidation of propanone involves the breaking of a carbon-carbon bond, leading to the formation of both formic acid and acetic acid.

Written and checked by , M.Phil ChemistryLast updated
Report an error

The more specific you are, the faster it gets fixed. A source beats an opinion.

Prefer email? [email protected]

About Carboxylic Acids

Carboxylic acids are named and studied through the combined effects of the carbonyl and hydroxyl groups, their preparation, acidity and hydrogen bonding. Reactions include neutralisation, esterification, reduction and conversion into acid chlorides, anhydrides, esters and amides, with emphasis on how these derivatives interconvert.

Practise Carboxylic Acids

550 free Carboxylic Acids MCQs from Chemistry, each with the correct answer and an explanation. Unlimited attempts, no account needed.

Discussion

Stuck on an option, or know a faster way to get there? Ask or explain it here.

No comments yet. Be the first to explain this one.

Exams that ask Chemistry questions like this

Chemistry is on 14 papers prepared for on TestUstad, and all of them draw the same bank, so this question is worth knowing for every one of them.

More Carboxylic Acids questions