The Claisen condensation converts two molecules of an ester into a ß-keto ester. The reaction starts with the ester in an alkoxide/alcohol solution and is worked up with acid to form the neutral ß-keto ester product. 1. "OCH,CH3 / CH3CH,OH 2 2. H3O* Show the curved-arrow mechanism for the Claisen condensation of ethyl ethanoate treated with ethoxide ion. Include all formal charges and nonbonding electrons. In each step, draw only the species that react in that step. If an enolate resonance form is possible, draw only the carbanionic form. If a CH; group is being deprotonated, draw all H's on the reacting site. Tip: always omit ethanol byproducts.
The Claisen condensation converts two molecules of an ester into a ß-keto ester. The reaction starts with the ester in an alkoxide/alcohol solution and is worked up with acid to form the neutral ß-keto ester product. 1. "OCH,CH3 / CH3CH,OH 2 2. H3O* Show the curved-arrow mechanism for the Claisen condensation of ethyl ethanoate treated with ethoxide ion. Include all formal charges and nonbonding electrons. In each step, draw only the species that react in that step. If an enolate resonance form is possible, draw only the carbanionic form. If a CH; group is being deprotonated, draw all H's on the reacting site. Tip: always omit ethanol byproducts.
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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Step 5b: Add curved arrows to show formation of the product

Transcribed Image Text:The Claisen condensation converts two molecules of an ester into a B-keto ester. The reaction starts with the ester in an
alkoxide/alcohol solution and is worked up with acid to form the neutral B-keto ester product.
1. "OCH2CH3/ CH3CH2OH
2. Hо*
Show the curved-arrow mechanism for the Claisen condensation of ethyl ethanoate treated with ethoxide ion. Include all
formal charges and nonbonding electrons. In each step, draw only the species that react in that step. If an enolate
resonance form is possible, draw only the carbanionic form. If a CHx group is being deprotonated, draw all H's on the
reacting site. Tip: always omit ethanol byproducts.
Step 5b: Add curved arrows to show formation of the product.
Select
Draw
Rings
More
Erase
: о :
:0 :
H
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