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What is/are the possible product(s) of dehydrohalogenation of cis-1-bromo-2-ethylcyclohexane? Et NaOMe Br A. В. C. D.

What is/are the possible product(s) of dehydrohalogenation of cis-1-bromo-2-ethylcyclohexane? Et NaOMe Br A. В. C. 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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### Dehydrohalogenation of cis-1-bromo-2-ethylcyclohexane **Question:** What is/are the possible product(s) of dehydrohalogenation of cis-1-bromo-2-ethylcyclohexane? **Provided Reaction:** Reactant: A cyclohexane ring with a bromo (Br) and ethyl (Et) group attached, forming 1-bromo-2-ethylcyclohexane in the cis configuration. Reagent: NaOMe (sodium methoxide) **Possible Products:** A. ![Option A](cyclohexene1.png) B. ![Option B](cyclohexene2.png) C. ![Option C](cyclohexene3.png) D. ![Option D](cyclohexene4.png) **Options for Answer:** - ◯ C - ◯ B - ◯ D - ◯ A **Explanation of Possible Products:** 1. **Product A:** A cyclohexane ring with a double bond between the carbon atoms 3 and 4, with an ethyl group at position 1. 2. **Product B:** A cyclohexane ring with a double bond between the carbon atoms 1 and 2, with an ethyl group at position 1. 3. **Product C:** A cyclohexane ring with a double bond between the carbon atoms 1 and 6, with an ethyl group at position 1. 4. **Product D:** Two structures, one cyclohexane ring with a double bond between the carbon atoms 1 and 2 with an ethyl group at position 1, and another cyclohexane ring with a double bond between carbon atoms 1 and 6. **Task:** Select the correct option representing the possible product(s) of the reaction. --- This transcription and explanation provide clarity on determining the result of the dehydrohalogenation reaction of cis-1-bromo-2-ethylcyclohexane with sodium methoxide (NaOMe).
Transcribed Image Text:### Dehydrohalogenation of cis-1-bromo-2-ethylcyclohexane **Question:** What is/are the possible product(s) of dehydrohalogenation of cis-1-bromo-2-ethylcyclohexane? **Provided Reaction:** Reactant: A cyclohexane ring with a bromo (Br) and ethyl (Et) group attached, forming 1-bromo-2-ethylcyclohexane in the cis configuration. Reagent: NaOMe (sodium methoxide) **Possible Products:** A. ![Option A](cyclohexene1.png) B. ![Option B](cyclohexene2.png) C. ![Option C](cyclohexene3.png) D. ![Option D](cyclohexene4.png) **Options for Answer:** - ◯ C - ◯ B - ◯ D - ◯ A **Explanation of Possible Products:** 1. **Product A:** A cyclohexane ring with a double bond between the carbon atoms 3 and 4, with an ethyl group at position 1. 2. **Product B:** A cyclohexane ring with a double bond between the carbon atoms 1 and 2, with an ethyl group at position 1. 3. **Product C:** A cyclohexane ring with a double bond between the carbon atoms 1 and 6, with an ethyl group at position 1. 4. **Product D:** Two structures, one cyclohexane ring with a double bond between the carbon atoms 1 and 2 with an ethyl group at position 1, and another cyclohexane ring with a double bond between carbon atoms 1 and 6. **Task:** Select the correct option representing the possible product(s) of the reaction. --- This transcription and explanation provide clarity on determining the result of the dehydrohalogenation reaction of cis-1-bromo-2-ethylcyclohexane with sodium methoxide (NaOMe).
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