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OB O C O A A. OD Which of the following is the most likely structure of the following cation after rearrangement? B.

OB O C O A A. OD Which of the following is the most likely structure of the following cation after rearrangement? B.

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 following is the most likely structure of the following cation after rearrangement? **Diagram:** The image displays a pentagon (cyclopentane ring) with a cation (+) symbol on a carbon atom connected to a methyl group, as the "following cation" that needs to be rearranged. **Options:** A. Cyclopentane ring with a cation (+) on a carbon next to where the methyl group was initially attached. B. Cyclopentane ring with a cation (+) on the same carbon where the methyl group is attached. C. Cyclopentane ring with a cation (+) on the carbon two positions away from where the methyl group is attached. D. Cyclohexane ring with a cation (+) on one of the carbons (after ring expansion). **Choices:** - ○ B - ○ C - ○ A - ○ D --- This question references the concept of carbocation rearrangements, which is a topic commonly covered in organic chemistry. Carbocations may undergo rearrangement to achieve a more stable carbocation formation, such as moving from a less stable 1° to 2° or 3° carbocation or through ring expansions like 5 to 6 member cyclical compounds.
Transcribed Image Text:**Question:** Which of the following is the most likely structure of the following cation after rearrangement? **Diagram:** The image displays a pentagon (cyclopentane ring) with a cation (+) symbol on a carbon atom connected to a methyl group, as the "following cation" that needs to be rearranged. **Options:** A. Cyclopentane ring with a cation (+) on a carbon next to where the methyl group was initially attached. B. Cyclopentane ring with a cation (+) on the same carbon where the methyl group is attached. C. Cyclopentane ring with a cation (+) on the carbon two positions away from where the methyl group is attached. D. Cyclohexane ring with a cation (+) on one of the carbons (after ring expansion). **Choices:** - ○ B - ○ C - ○ A - ○ D --- This question references the concept of carbocation rearrangements, which is a topic commonly covered in organic chemistry. Carbocations may undergo rearrangement to achieve a more stable carbocation formation, such as moving from a less stable 1° to 2° or 3° carbocation or through ring expansions like 5 to 6 member cyclical compounds.
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