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What is the major product to the following reaction? 1. NaNH2 Br 2.

What is the major product to the following reaction? 1. NaNH2 Br 2.

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:** What is the major product of the following reaction? **Reaction Details:** 1. Starting Material: A molecule featuring an alkyne group attached to a branching alkyl group. 2. Reagents: - Step 1: NaNH₂ - Step 2: A molecule with a bromine atom attached to a branching alkyl group. **Answer Choices:** - Option A: A molecule with an alkene group attached to a branching alkyl group. - Option B: A molecule with a longer carbon chain featuring two branching points and an alkene group. - Option C: A molecule with an alkene group attached at one end to a branching point, forming a shorter chain than Option B. **Explanation:** This question involves using a base (NaNH₂) to generate an acetylide ion from the terminal alkyne, which then participates in a nucleophilic substitution reaction with the alkyl bromide to form a new carbon-carbon bond.
Transcribed Image Text:**Question:** What is the major product of the following reaction? **Reaction Details:** 1. Starting Material: A molecule featuring an alkyne group attached to a branching alkyl group. 2. Reagents: - Step 1: NaNH₂ - Step 2: A molecule with a bromine atom attached to a branching alkyl group. **Answer Choices:** - Option A: A molecule with an alkene group attached to a branching alkyl group. - Option B: A molecule with a longer carbon chain featuring two branching points and an alkene group. - Option C: A molecule with an alkene group attached at one end to a branching point, forming a shorter chain than Option B. **Explanation:** This question involves using a base (NaNH₂) to generate an acetylide ion from the terminal alkyne, which then participates in a nucleophilic substitution reaction with the alkyl bromide to form a new carbon-carbon bond.
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