#30 help ### Reaction Transformation Exercise**Objective:** Draw the major product of the given chemical reaction. Omit any inorganic byproducts and the amine side product.#### Reaction Details:- **Starting Material:** A molecule containing an amide functional group is shown, represented with a carbonyl group (C=O) attached to a nitrogen atom (N). - **Reaction Conditions:** 1. **Reagent:** NaOH (sodium hydroxide) 2. **Condition:** Heat is applied. 3. **Subsequent Step:** Neutralizing work-up is performed.**Instructions:** Using the provided reaction conditions, predict and draw the major organic product of the reaction focusing primarily on the transformations occurring to the amide group.### Graphical Representation:- An arrow is depicted indicating a transformation from the starting amide structure to the product after the reaction steps.**Important Notes:**- The focus is on the organic product excluding the formation of inorganic salts or minor amine byproducts.- The reaction likely involves hydrolysis of the amide, resulting in conversion to a carboxylate salt, which is then neutralized to form a carboxylic acid. This transcription is intended for educational purposes to help students understand chemical reaction mechanisms and predict reaction outcomes.

Hydrolysis of amide by base to form carboxylic acid.. This reaction involves two steps nucleophilic…

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Chemistry

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Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

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#30 help

### Reaction Transformation Exercise

**Objective:** Draw the major product of the given chemical reaction. Omit any inorganic byproducts and the amine side product.

#### Reaction Details:

- **Starting Material:** A molecule containing an amide functional group is shown, represented with a carbonyl group (C=O) attached to a nitrogen atom (N).

- **Reaction Conditions:**
1. **Reagent:** NaOH (sodium hydroxide)
2. **Condition:** Heat is applied.
3. **Subsequent Step:** Neutralizing work-up is performed.

**Instructions:** Using the provided reaction conditions, predict and draw the major organic product of the reaction focusing primarily on the transformations occurring to the amide group.

### Graphical Representation:

- An arrow is depicted indicating a transformation from the starting amide structure to the product after the reaction steps.

**Important Notes:**
- The focus is on the organic product excluding the formation of inorganic salts or minor amine byproducts.
- The reaction likely involves hydrolysis of the amide, resulting in conversion to a carboxylate salt, which is then neutralized to form a carboxylic acid.

This transcription is intended for educational purposes to help students understand chemical reaction mechanisms and predict reaction outcomes.

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