Predict the product of the hydroboration-oxidation reaction shown below. 1. Вн, THF 2. H2O2/NaOH O a. но O b. HO но. O d.

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**Hydroboration-Oxidation Reaction Product Prediction**

**Question:**
Predict the product of the hydroboration-oxidation reaction shown below.

**Reaction:**
- Starting compound: A cyclohexene derivative with a methyl group attached to the ring.
- Step 1: BH₃, THF
- Step 2: H₂O₂/NaOH

**Possible Products:**
- **Option a**: Cyclohexyl ring with a hydroxyl group (OH) attached to the carbon next to the methyl group.
- **Option b**: Cyclohexyl ring with a hydroxyl group (OH) on the carbon between the methyl and double bond.
- **Option c**: Cyclohexyl ring with two hydroxyl groups (OH) on adjacent carbons.
- **Option d**: Cyclohexyl ring with a hydroxyl group (OH) attached to a carbon adjacent to the methyl group.

**Explanation:**
The hydroboration-oxidation reaction involves an anti-Markovnikov addition of water across the double bond, resulting in the addition of a hydroxyl group at the less substituted carbon of the double bond.
Transcribed Image Text:**Hydroboration-Oxidation Reaction Product Prediction** **Question:** Predict the product of the hydroboration-oxidation reaction shown below. **Reaction:** - Starting compound: A cyclohexene derivative with a methyl group attached to the ring. - Step 1: BH₃, THF - Step 2: H₂O₂/NaOH **Possible Products:** - **Option a**: Cyclohexyl ring with a hydroxyl group (OH) attached to the carbon next to the methyl group. - **Option b**: Cyclohexyl ring with a hydroxyl group (OH) on the carbon between the methyl and double bond. - **Option c**: Cyclohexyl ring with two hydroxyl groups (OH) on adjacent carbons. - **Option d**: Cyclohexyl ring with a hydroxyl group (OH) attached to a carbon adjacent to the methyl group. **Explanation:** The hydroboration-oxidation reaction involves an anti-Markovnikov addition of water across the double bond, resulting in the addition of a hydroxyl group at the less substituted carbon of the double bond.
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