Choose the reagent(s) that would be most likely to complete this reaction. LL K H A B D E BH3-THF H2O2, NaOH tBuOK CHCI 3 CH₂I2 Zn/Cu mCPBA 1. Hg(OAc)2, H₂O 2. NaBH4, NaOH

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Chapter1: Chemical Foundations
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### Reaction Completion Problem

**Prompt**: Choose the reagent(s) that would be most likely to complete this reaction.

**Diagram Explanation**:
- **Top Structure**: A molecule with a carbon-carbon double bond, likely representing an alkene.
- **Bottom Structure**: A three-membered carbon ring (cyclopropane) with two hydrogen atoms attached to one of the carbons via wedge bonds, indicating they are coming out of the plane.

**Reagent Options**:
- **A**: BH₃-THF followed by H₂O₂, NaOH
- **B**: tBuOK, CHCl₃
- **C**: CH₂I₂, Zn/Cu
- **D**: mCPBA
- **E**: 
  1. Hg(OAc)₂, H₂O
  2. NaBH₄, NaOH

**Selected Reagent**: **B** - tBuOK and CHCl₃

The selected reagent, **B**, suggests the use of tBuOK and CHCl₃, indicating a reaction pathway that could lead to the formation of a cyclopropane through a base-induced cyclopropanation process known as the Simmons-Smith reaction.
Transcribed Image Text:### Reaction Completion Problem **Prompt**: Choose the reagent(s) that would be most likely to complete this reaction. **Diagram Explanation**: - **Top Structure**: A molecule with a carbon-carbon double bond, likely representing an alkene. - **Bottom Structure**: A three-membered carbon ring (cyclopropane) with two hydrogen atoms attached to one of the carbons via wedge bonds, indicating they are coming out of the plane. **Reagent Options**: - **A**: BH₃-THF followed by H₂O₂, NaOH - **B**: tBuOK, CHCl₃ - **C**: CH₂I₂, Zn/Cu - **D**: mCPBA - **E**: 1. Hg(OAc)₂, H₂O 2. NaBH₄, NaOH **Selected Reagent**: **B** - tBuOK and CHCl₃ The selected reagent, **B**, suggests the use of tBuOK and CHCl₃, indicating a reaction pathway that could lead to the formation of a cyclopropane through a base-induced cyclopropanation process known as the Simmons-Smith reaction.
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