CH3 CH3 2 C 6 H 5 Mg Br H₂0+ О CH3

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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What is the product
This image represents a chemical reaction involving a ketone and a Grignard reagent. 

**Chemical Equation:**

1. **Reactant:** A ketone with the structure (CH₃)₂C=O (acetone).

2. **Reagents:**
   - 2 equivalents of phenylmagnesium bromide (C₆H₅MgBr)
   - Water (H₂O)

**Reaction Description:**

- The image shows an arrow indicating the reaction direction with the reagents listed above the arrow.
- The ketone undergoes nucleophilic addition, where the Grignard reagent (phenylmagnesium bromide) adds to the carbonyl carbon of acetone.
- After the addition, hydrolysis with water typically follows, leading to the formation of an alcohol.

**Note:**
- Grignard reactions are a staple in organic chemistry, widely used to form carbon-carbon bonds.
Transcribed Image Text:This image represents a chemical reaction involving a ketone and a Grignard reagent. **Chemical Equation:** 1. **Reactant:** A ketone with the structure (CH₃)₂C=O (acetone). 2. **Reagents:** - 2 equivalents of phenylmagnesium bromide (C₆H₅MgBr) - Water (H₂O) **Reaction Description:** - The image shows an arrow indicating the reaction direction with the reagents listed above the arrow. - The ketone undergoes nucleophilic addition, where the Grignard reagent (phenylmagnesium bromide) adds to the carbonyl carbon of acetone. - After the addition, hydrolysis with water typically follows, leading to the formation of an alcohol. **Note:** - Grignard reactions are a staple in organic chemistry, widely used to form carbon-carbon bonds.
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