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Identify the carbocation intermediates first formed in the following reaction. Will rearrangements possibly occur? What major product is formed? 8 HCI

Identify the carbocation intermediates first formed in the following reaction. Will rearrangements possibly occur? What major product is formed? 8 HCI

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:** Identify the carbocation intermediates first formed in the following reaction. Will rearrangements possibly occur? What major product is formed? **Reaction:** A cyclohexene derivative with a methyl group attached is shown reacting with HCl. **Explanation:** When HCl reacts with the given alkene, the double bond breaks, and a carbocation intermediate is formed. The initial carbocation will likely form at the more stable position. If the initial carbocation is not the most stable form, a rearrangement may occur to form a more stable carbocation. The Cl⁻ ion will then attack the carbocation, resulting in the formation of the major product, which is an alkyl chloride.
Transcribed Image Text:**Question:** Identify the carbocation intermediates first formed in the following reaction. Will rearrangements possibly occur? What major product is formed? **Reaction:** A cyclohexene derivative with a methyl group attached is shown reacting with HCl. **Explanation:** When HCl reacts with the given alkene, the double bond breaks, and a carbocation intermediate is formed. The initial carbocation will likely form at the more stable position. If the initial carbocation is not the most stable form, a rearrangement may occur to form a more stable carbocation. The Cl⁻ ion will then attack the carbocation, resulting in the formation of the major product, which is an alkyl chloride.
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