Please draw the mechanism for the following reaction. The first step in the reaction mechanism is the formation of a carbocation intermediate (shown), followed by a carbocation rearrangement. Which bond moves in the carbocation rearrangement? Which compound shown below has that appropriate bond in pink? A H₂SO4 H₂O Carbocation intermediate H B OH

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The image describes a chemical reaction mechanism involving the formation of a carbocation intermediate and its subsequent rearrangement.

Text:
"Please draw the mechanism for the following reaction. The first step in the reaction mechanism is the formation of a carbocation intermediate (shown), followed by a carbocation rearrangement. Which bond moves in the carbocation rearrangement? Which compound shown below has that appropriate bond in pink?"

Diagrams:
- **Structure A** (reactant):
  - Features a cycloheptene ring with a methyl substituent.
  - Reaction conditions include H₂SO₄ and H₂O, suggesting an acid-catalyzed hydration reaction.

- **Structure B** (product):
  - Shows a cycloheptane ring with an alcohol (OH) group and a methyl substituent.

- **Carbocation Intermediate**:
  - Highlights a seven-membered ring with a positively charged carbon (carbocation) and an adjacent hydrogen.

The reaction demonstrates the transformation of a double bond into an alcohol via addition, showcasing a rearrangement to stabilize the carbocation intermediate, a key concept in organic chemistry mechanisms.
Transcribed Image Text:The image describes a chemical reaction mechanism involving the formation of a carbocation intermediate and its subsequent rearrangement. Text: "Please draw the mechanism for the following reaction. The first step in the reaction mechanism is the formation of a carbocation intermediate (shown), followed by a carbocation rearrangement. Which bond moves in the carbocation rearrangement? Which compound shown below has that appropriate bond in pink?" Diagrams: - **Structure A** (reactant): - Features a cycloheptene ring with a methyl substituent. - Reaction conditions include H₂SO₄ and H₂O, suggesting an acid-catalyzed hydration reaction. - **Structure B** (product): - Shows a cycloheptane ring with an alcohol (OH) group and a methyl substituent. - **Carbocation Intermediate**: - Highlights a seven-membered ring with a positively charged carbon (carbocation) and an adjacent hydrogen. The reaction demonstrates the transformation of a double bond into an alcohol via addition, showcasing a rearrangement to stabilize the carbocation intermediate, a key concept in organic chemistry mechanisms.
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