Draw the products of the following reactions, indicating both regiochemistry and stereochemistry when appropriate. CH3 1. Hg(OAc)2, H2O 2. NaBH4 • Use wedge and hash bonds ONLY when needed to show reaction stereochemistry. In cases where there is more than one answer, just draw one. Visited opy aste ChemDoodle

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Chapter1: Chemical Foundations
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**Instruction:**

Draw the products of the following reactions, indicating both regiochemistry and stereochemistry when appropriate.

**Chemical Reaction:**

Reactant:
- A benzene ring with a methyl group (CH₃) attached.

Reagents:
1. \( \text{Hg(OAc)}_2, \text{H}_2\text{O} \)
2. \( \text{NaBH}_4 \)

**Guidelines:**

- Use wedge and hash bonds ONLY when needed to show reaction stereochemistry.
- In cases where there is more than one answer, just draw one.

**Diagram Tool:**

A blank ChemDoodle workspace is shown below the instructions, with a toolbar containing various drawing tools and molecular structure components.

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Explanation: This involves an organic reaction starting with a benzene ring with a methyl substituent undergoing a two-step reaction. The process likely involves oxymercuration-demercuration, which adds a hydroxyl group (OH) to the less-substituted carbon, following Markovnikov's rule. Stereochemistry should be indicated using wedge and dashed bonds when necessary.
Transcribed Image Text:Sure, here is a transcription of the image content: --- **Instruction:** Draw the products of the following reactions, indicating both regiochemistry and stereochemistry when appropriate. **Chemical Reaction:** Reactant: - A benzene ring with a methyl group (CH₃) attached. Reagents: 1. \( \text{Hg(OAc)}_2, \text{H}_2\text{O} \) 2. \( \text{NaBH}_4 \) **Guidelines:** - Use wedge and hash bonds ONLY when needed to show reaction stereochemistry. - In cases where there is more than one answer, just draw one. **Diagram Tool:** A blank ChemDoodle workspace is shown below the instructions, with a toolbar containing various drawing tools and molecular structure components. --- Explanation: This involves an organic reaction starting with a benzene ring with a methyl substituent undergoing a two-step reaction. The process likely involves oxymercuration-demercuration, which adds a hydroxyl group (OH) to the less-substituted carbon, following Markovnikov's rule. Stereochemistry should be indicated using wedge and dashed bonds when necessary.
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