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3. Treatment of 1-phenyl-2-propenone with a strong base such as LDA does not yield an anion, even though it contains a hydrogen on the carbon atom next to the carbonyl group. Explain. H CH₂ 1-Phenyl-2-propenone

3. Treatment of 1-phenyl-2-propenone with a strong base such as LDA does not yield an anion, even though it contains a hydrogen on the carbon atom next to the carbonyl group. Explain. H CH₂ 1-Phenyl-2-propenone

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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3. Treatment of 1-phenyl-2-propenone with a strong base such as LDA does not yield an anion, even though it contains a hydrogen on the carbon atom next to the carbonyl group. Explain. (a) Ethyl pentanoate H Ethyl 2-methylbutanoate CH₂ . Which of the following compounds can be prepared by a malonic ester synthesis? Show the alkyl halide you would use in each case. 1-Phenyl-2-propenone (b) Ethyl 3-methylbutanoate (d) Ethyl 2,2-dimethylpropanoate
Transcribed Image Text:3. Treatment of 1-phenyl-2-propenone with a strong base such as LDA does not yield an anion, even though it contains a hydrogen on the carbon atom next to the carbonyl group. Explain. (a) Ethyl pentanoate H Ethyl 2-methylbutanoate CH₂ . Which of the following compounds can be prepared by a malonic ester synthesis? Show the alkyl halide you would use in each case. 1-Phenyl-2-propenone (b) Ethyl 3-methylbutanoate (d) Ethyl 2,2-dimethylpropanoate
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