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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
Transcribed Image Text:**Question:**
What is the major product for the following reaction?
**Reaction Details:**
The starting compound is a structure with an -OTs group (tosylate) and a -CH₃ group. The reaction involves KOH as a reagent.
**Options:**
1. **Option A:** A structure with a double bond between two carbons, forming an alkene, without any additional branches or groups.
2. **Option B:** A structure featuring a -CH₃ branch on the second carbon with an alkene between the first and second carbon.
3. **Option C:** A structure with a -CH₃ branch on the second carbon, featuring an alkene bond between the second and third carbon.
4. **Option D:** A structure with a more complex branching pattern and an alkene.
**Save for Later Button:**
- An option to save the question for later review.
**Explanation:**
The question involves predicting the major product of an elimination reaction with KOH, which typically leads to a formation of an alkene. Understanding the position and type of groups attached is crucial to determine which option is the correct major product based on Zaitsev's rule or other applicable rules.
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