What order of reagents should be used to synthesize the following product from methylcyclopentane? (A) Br2 (B) Br2, hv (C) КОН, Һeat Br (racemic) Br C, then B, then A B, then A, then C C, then A, then B O B, then C, then A O A, then B, then C O A, then C, then B
What order of reagents should be used to synthesize the following product from methylcyclopentane? (A) Br2 (B) Br2, hv (C) КОН, Һeat Br (racemic) Br C, then B, then A B, then A, then C C, then A, then B O B, then C, then A O A, then B, then C O A, then C, then B
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 order of reagents should be used to synthesize the following product from methylcyclopentane?
**Reagents:**
(A) Br₂
(B) Br₂, hv
(C) KOH, heat
**Diagram Explanation:**
- The starting material is methylcyclopentane, depicted as a cyclopentane ring with a methyl group.
- The product is a brominated cyclopentane with two bromine atoms attached, indicated as a racemic mixture with one bromine atom on each side of the ring.
**Options:**
- ○ C, then B, then A
- ○ B, then A, then C
- ○ C, then A, then B
- ● B, then C, then A
- ○ A, then B, then C
- ○ A, then C, then B
**Correct Answer:**
B, then C, then A
In this synthesis, initiating with bromination using light (Br₂, hv) introduces bromine radicals, followed by elimination with KOH and heat, and concluding with the addition of Br₂ creates the final dibromide product.
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