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Which of the compounds below is the major product of the following reaction? Na ether Compound A Compound B Compound C Compound D Compound A Compound C Compound B Compound D

Which of the compounds below is the major product of the following reaction? Na ether Compound A Compound B Compound C Compound D Compound A Compound C Compound B Compound D

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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**Question:** Which of the compounds below is the major product of the following reaction? **Reaction:** Cyclohexanone enolate anion (shown as a ring with an O⁻) with sodium (Na⁺) is reacting with 1-bromo-2-methylpropane in the presence of ether. **Possible Products:** - **Compound A**: Cyclohexanone ring attached to a butyl group. - **Compound B**: Cyclohexanone ring attached to a secondary butyl group. - **Compound C**: An alkene with a propyl group and a methyl group on the alkene carbon. - **Compound D**: A different alkene with a propyl group. **Options:** - ○ Compound A - ○ Compound C - ○ Compound B - ○ Compound D **Explanation of Reaction:** This reaction likely involves the nucleophilic attack of the enolate anion on the bromoalkane leading to substitution or elimination, depending on conditions, to form ether-stabilized products.
Transcribed Image Text:**Question:** Which of the compounds below is the major product of the following reaction? **Reaction:** Cyclohexanone enolate anion (shown as a ring with an O⁻) with sodium (Na⁺) is reacting with 1-bromo-2-methylpropane in the presence of ether. **Possible Products:** - **Compound A**: Cyclohexanone ring attached to a butyl group. - **Compound B**: Cyclohexanone ring attached to a secondary butyl group. - **Compound C**: An alkene with a propyl group and a methyl group on the alkene carbon. - **Compound D**: A different alkene with a propyl group. **Options:** - ○ Compound A - ○ Compound C - ○ Compound B - ○ Compound D **Explanation of Reaction:** This reaction likely involves the nucleophilic attack of the enolate anion on the bromoalkane leading to substitution or elimination, depending on conditions, to form ether-stabilized products.
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