Br MgBr (1 eq.), Et₂O

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
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Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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This image is a representation of a chemical reaction involving a Grignard reagent. The starting material is a bromo ketone, specifically:

- The left side of the equation depicts a molecule with a bromine (Br) attached to a 4-carbon aldehyde with a ketone (C=O) group.

The reaction conditions and reagents are as follows:

- The Grignard reagent is ethylmagnesium bromide (EtMgBr) at 1 equivalent.
- The solvent used is diethyl ether (Et₂O).

Arrow indicating the transformation:
- The arrow points from the reactants to the right, indicating the progression of the reaction where the Grignard reagent will react with the ketone, leading to the formation of a new alcohol product. This reaction is typically a nucleophilic addition.

Overall, this setup is aimed at demonstrating the reaction of a Grignard reagent with a ketone to form an alcohol, a common and essential type of reaction in organic synthesis.
Transcribed Image Text:This image is a representation of a chemical reaction involving a Grignard reagent. The starting material is a bromo ketone, specifically: - The left side of the equation depicts a molecule with a bromine (Br) attached to a 4-carbon aldehyde with a ketone (C=O) group. The reaction conditions and reagents are as follows: - The Grignard reagent is ethylmagnesium bromide (EtMgBr) at 1 equivalent. - The solvent used is diethyl ether (Et₂O). Arrow indicating the transformation: - The arrow points from the reactants to the right, indicating the progression of the reaction where the Grignard reagent will react with the ketone, leading to the formation of a new alcohol product. This reaction is typically a nucleophilic addition. Overall, this setup is aimed at demonstrating the reaction of a Grignard reagent with a ketone to form an alcohol, a common and essential type of reaction in organic synthesis.
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