Draw the reaction product for the following SN 2 reaction: Br. \SH NaSH What is the best description of the product(s) that form? O single enantiomer O achiral product O pair of enantiomers O pair of diastereomers

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**Title: Understanding SN2 Reactions: A Detailed Overview**

**Text:**

*Draw the reaction product for the following SN2 reaction:*

The image depicts a cyclohexane ring with a bromine (Br) atom attached to one of the carbon atoms and an SH (thiol) group also attached, showing stereochemistry with a wedge bond. Sodium hydrosulfide (NaSH) is indicated as the reagent, leading to the reaction arrow suggesting a nucleophilic substitution reaction.

**Question:**
What is the best description of the product(s) that form?

- ○ single enantiomer
- ● achiral product
- ○ pair of enantiomers
- ○ pair of diastereomers

**Explanation:**

In this specific SN2 reaction, the nucleophile (NaSH) attacks the electrophilic carbon atom attached to the bromine, resulting in the substitution of the bromine with the thiol group. SN2 reactions typically proceed with inversion of configuration, leading to the formation of a potentially achiral product, given the symmetrical nature of the starting material. 

In this case, the correct answer is “achiral product,” as indicated by the selected option.
Transcribed Image Text:**Title: Understanding SN2 Reactions: A Detailed Overview** **Text:** *Draw the reaction product for the following SN2 reaction:* The image depicts a cyclohexane ring with a bromine (Br) atom attached to one of the carbon atoms and an SH (thiol) group also attached, showing stereochemistry with a wedge bond. Sodium hydrosulfide (NaSH) is indicated as the reagent, leading to the reaction arrow suggesting a nucleophilic substitution reaction. **Question:** What is the best description of the product(s) that form? - ○ single enantiomer - ● achiral product - ○ pair of enantiomers - ○ pair of diastereomers **Explanation:** In this specific SN2 reaction, the nucleophile (NaSH) attacks the electrophilic carbon atom attached to the bromine, resulting in the substitution of the bromine with the thiol group. SN2 reactions typically proceed with inversion of configuration, leading to the formation of a potentially achiral product, given the symmetrical nature of the starting material. In this case, the correct answer is “achiral product,” as indicated by the selected option.
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