CH3O- CH;OH

Chemistry
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ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
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Chapter1: Chemical Foundations
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Please draw the structure of the neutral product formed in the reaction of dimethyl malonate and methyl vinyl ketone, thank you

### Aldol Reaction Mechanism

The image depicts a chemical reaction involving a β-keto ester and an enolate ion (CH₃O⁻) in a base-catalyzed aldol reaction.

#### Reactants:
1. **β-Keto Ester**:
   - Structure: Contains two ester groups (–COO–) connected by a two-carbon chain.
   - Functionality: Acts as an electrophile in the reaction.

2. **Enolate Ion (CH₃O⁻)**:
   - Structure: Methoxide ion.
   - Role: Serves as a base to deprotonate an acidic alpha hydrogen, forming an enolate.

3. **Aldehyde**:
   - Structure: Contains a carbonyl group (C=O) with a vinyl group attached.
   - Reactivity: Acts as an electrophile in the subsequent aldol addition step.

#### Reaction Overview:
- The methoxide ion (CH₃O⁻) deprotonates the acidic hydrogen adjacent to the keto group, forming an enolate ion.
- The enolate ion acts as a nucleophile, attacking the carbonyl carbon of the aldehyde.
- This nucleophilic addition forms a β-hydroxy ester intermediate (not shown in the image).

#### Product:
- **Methanol (CH₃OH)**:
  - The reaction results in the formation of methanol as a byproduct.

This reaction demonstrates crucial concepts in organic chemistry related to carbonyl chemistry and enolate reactivity, aiding in the synthesis of complex molecules.
Transcribed Image Text:### Aldol Reaction Mechanism The image depicts a chemical reaction involving a β-keto ester and an enolate ion (CH₃O⁻) in a base-catalyzed aldol reaction. #### Reactants: 1. **β-Keto Ester**: - Structure: Contains two ester groups (–COO–) connected by a two-carbon chain. - Functionality: Acts as an electrophile in the reaction. 2. **Enolate Ion (CH₃O⁻)**: - Structure: Methoxide ion. - Role: Serves as a base to deprotonate an acidic alpha hydrogen, forming an enolate. 3. **Aldehyde**: - Structure: Contains a carbonyl group (C=O) with a vinyl group attached. - Reactivity: Acts as an electrophile in the subsequent aldol addition step. #### Reaction Overview: - The methoxide ion (CH₃O⁻) deprotonates the acidic hydrogen adjacent to the keto group, forming an enolate ion. - The enolate ion acts as a nucleophile, attacking the carbonyl carbon of the aldehyde. - This nucleophilic addition forms a β-hydroxy ester intermediate (not shown in the image). #### Product: - **Methanol (CH₃OH)**: - The reaction results in the formation of methanol as a byproduct. This reaction demonstrates crucial concepts in organic chemistry related to carbonyl chemistry and enolate reactivity, aiding in the synthesis of complex molecules.
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