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3 2. 강 H+ acidic work-up

3 2. 강 H+ acidic work-up

Chemistry
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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In the image, a chemical reaction is depicted. The starting material is cyclopentanone. The reaction involves two steps: 1. Cyclopentanone reacts with pyrrolidine in the presence of an acid catalyst (H⁺). 2. The intermediate product is then reacted with acetyl chloride. The reaction involves an acidic work-up to yield the final product, denoted as compound J. This is likely an example of an amine-catalyzed acylation reaction, which involves forming an iminium ion intermediate followed by nucleophilic acyl substitution. The final product structure is not shown.
Transcribed Image Text:In the image, a chemical reaction is depicted. The starting material is cyclopentanone. The reaction involves two steps: 1. Cyclopentanone reacts with pyrrolidine in the presence of an acid catalyst (H⁺). 2. The intermediate product is then reacted with acetyl chloride. The reaction involves an acidic work-up to yield the final product, denoted as compound J. This is likely an example of an amine-catalyzed acylation reaction, which involves forming an iminium ion intermediate followed by nucleophilic acyl substitution. The final product structure is not shown.
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