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Which of the following name reactions is not used for introducing a \[COOH\] group?
(A) Cannizzaro reaction
(B) Benzilic acid rearrangement
(C) Baeyer- Villiger oxidation
(D) Iodoform reaction

Last updated date: 20th Jun 2024
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Hint: In the question, four name reactions have been mentioned and we need to choose the reaction which doesn’t introduce a carboxylic acid functional group in the product. Write the general reaction for each of the name reactions and then identify the reaction which does not introduce carboxylic acid in the product.

Complete step by step answer:
- Let’s begin by writing the general reactions of all the name reactions given in the options.
- Cannizzaro reaction is a reaction in which two molecules of carbonyl compounds having absence of $\alpha $-hydrogen atoms undergo disproportionation reaction in the presence of a base and on acid hydrolysis, form an alcohol and a carboxylic acid. One of the examples of this reaction is,
- Benzilic acid rearrangement reaction involves conversion of a 1,2-diketone into $\alpha $-hydroxycarboxylic acid in the presence of a strong base followed by acid hydrolysis.
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- Baeyer- Villiger oxidation is an oxidation reaction in which a ketone is converted into an ester due to addition of one oxygen atom in the chain. Here, m-chloroperoxybenzoic acid is used as an oxidizing agent.
- Iodoform reaction is a reaction in which a compound containing acetyl group is oxidized into salt of acetic acid due to the action of iodine in basic condition. The salt can be acidified to form carboxylic acid.
- Therefore, Baeyer-Villiger rearrangement reaction is the only name reaction in the given options which doesn’t form carboxylic acid. So, the correct answer is “Option C”.

Note: Remember the important name reactions in organic chemistry. Remember to convert ketone to ester, Baeyer-Villiger rearrangement reaction is used. Iodoform reaction will be given by compounds containing methoxy ketone group and ethanol and isopropanol or sec-alcohols which form methoxy ketones on oxidation.