what would be the answer? **Claisen Condensation Reaction Analysis**Would you predict that the Claisen condensation reaction shown below would work as written?**Reaction Setup:**The reaction starts with a cyclohexanone compound (a six-membered cyclic ketone) on the left. 1. Reagents: - **LDA, –78 °C** (Lithium diisopropylamide, a strong base, used at low temperature) - The second step introduces an ester with the structure: \[ \text{MeO} \overset{\text{O}}{\vert} \text{C} \text{CH}_2 \text{CH}_2 \text{CH}_3 \]**Expected Product:**The product shown on the right is a β-keto ester:- A ring structure with a ketone and an ester group separated by one CH2 group.**Question:**- Options: - No - YesSelect whether you think the Claisen condensation, with the steps and conditions provided, would successfully yield the expected β-keto ester product.

Claisen condensation is the reaction between an ester and a ketone or between two esters in the presence of a base to form a beta-diketone.When a carbonyl compound reacts with an ester in the presence of a base,we get a beta-diketone which is formed by the removal of proton from beta position of carbonyl and removal of alkoxy group from the ester group. The same is occurring in the given reaction and hence,yes,the given reaction is the same as predicted.

Answered: Would you predict that the Claisen…

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Would you predict that the Claisen condensation reaction shown below would work as written? 1. LDA, –78 °C 2. MeO No Yes

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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