What is the name of the product of this reaction? CH3 2 Mg H3C H,0 H3C. Br 2.

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### What is the name of the product of this reaction?

The chemical reaction depicted involves the following steps:

1. **Starting Compound**: The reaction begins with 1-bromopropane (CH3CH2CH2Br).

2. **Reagent**: The first step involves the use of magnesium (Mg), likely forming a Grignard reagent.

3. **Intermediate**: The reaction continues with the Grignard reagent interacting with a ketone, shown as:
   \[
   \text{CH}_3\text{C(O)OCH}_3
   \]
   This represents a methyl ester.

4. **Acid Workup**: The final step involves an acid workup using hydronium ion (\( \text{H}_3\text{O}^+ \)).

### Explanation

- **First Step**: Formation of a Grignard reagent (R-Mg-Br) from the alkyl bromide with Mg.
- **Second Step**: Grignard addition to the carbonyl carbon of the ester to form an intermediate alcohol.
- **Third Step**: Protonation (via the acid workup) to yield the final alcohol product.

The reaction sequence demonstrates the conversion of an alkyl bromide to an alcohol, showcasing the functionality of Grignard reagents in forming carbon-carbon bonds and transforming functional groups.

The final product of this reaction would typically be termed based on IUPAC naming for alcohols, following the formation of a new carbon chain linked by the Grignard addition.
Transcribed Image Text:### What is the name of the product of this reaction? The chemical reaction depicted involves the following steps: 1. **Starting Compound**: The reaction begins with 1-bromopropane (CH3CH2CH2Br). 2. **Reagent**: The first step involves the use of magnesium (Mg), likely forming a Grignard reagent. 3. **Intermediate**: The reaction continues with the Grignard reagent interacting with a ketone, shown as: \[ \text{CH}_3\text{C(O)OCH}_3 \] This represents a methyl ester. 4. **Acid Workup**: The final step involves an acid workup using hydronium ion (\( \text{H}_3\text{O}^+ \)). ### Explanation - **First Step**: Formation of a Grignard reagent (R-Mg-Br) from the alkyl bromide with Mg. - **Second Step**: Grignard addition to the carbonyl carbon of the ester to form an intermediate alcohol. - **Third Step**: Protonation (via the acid workup) to yield the final alcohol product. The reaction sequence demonstrates the conversion of an alkyl bromide to an alcohol, showcasing the functionality of Grignard reagents in forming carbon-carbon bonds and transforming functional groups. The final product of this reaction would typically be termed based on IUPAC naming for alcohols, following the formation of a new carbon chain linked by the Grignard addition.
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