Draw the major product of this reaction. Ignore inorganic byproducts and the amine side product. 'N H 1. H3O+, heat 2. Neutralizing work-up O OH D

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Chapter1: Chemical Foundations
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### Reaction Overview

**Objective:**
Draw the major product of the reaction, ignoring inorganic byproducts and the amine side product.

**Starting Material:**
- A cyclic amide (shown in inset diagram) with a six-membered ring with one carbonyl group (C=O) and an NH group.

**Reagents:**
1. \( \text{H}_3\text{O}^+ \), heat
2. Neutralizing work-up

**Product Structure:**
- The major product is benzoic acid, depicted as a benzene ring attached to a carboxyl group (COOH).

### Explanation of Diagrams

- **Starting Material Structure:**
  - The structure depicted within a small box shows a cyclohexanone derivative with an amide group.

- **Arrow Flow Chart:**
  - A downward arrow indicates the reaction's progress leading to the major product after treatment with the given reagents.

### Reaction Conditions and Specified Outcome:

- Acidic hydrolysis under heat converts the cyclic amide to its corresponding carboxylic acid. The results are presented as a benzene ring bonded to a carboxyl group.
Transcribed Image Text:### Reaction Overview **Objective:** Draw the major product of the reaction, ignoring inorganic byproducts and the amine side product. **Starting Material:** - A cyclic amide (shown in inset diagram) with a six-membered ring with one carbonyl group (C=O) and an NH group. **Reagents:** 1. \( \text{H}_3\text{O}^+ \), heat 2. Neutralizing work-up **Product Structure:** - The major product is benzoic acid, depicted as a benzene ring attached to a carboxyl group (COOH). ### Explanation of Diagrams - **Starting Material Structure:** - The structure depicted within a small box shows a cyclohexanone derivative with an amide group. - **Arrow Flow Chart:** - A downward arrow indicates the reaction's progress leading to the major product after treatment with the given reagents. ### Reaction Conditions and Specified Outcome: - Acidic hydrolysis under heat converts the cyclic amide to its corresponding carboxylic acid. The results are presented as a benzene ring bonded to a carboxyl group.
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