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

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**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.
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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