Draw the product of an SN2 reaction shown below. Use wedge and dash bonds to indicate stereochemistry where appropriate. Ignore inorganic byproducts. NaSCH3. THF Drawing Br

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**Title: Understanding the SN2 Reaction Mechanism**

**Objective:**
Draw the product of an SN2 reaction using the given reactants. Use wedge and dash bonds to indicate stereochemistry where appropriate. Inorganic byproducts should be ignored.

**Reactants:**
- The starting molecule is a bromide compound represented with a straight-chain hydrocarbon skeleton.
- The bromine atom (Br) is attached to the terminal carbon of the chain with a wedge bond, indicating its stereochemistry.

**Reagents:**
- Sodium methanethiolate (NaSCH₃)
- Tetrahydrofuran (THF) as the solvent

**Diagram Explanation:**
The diagram needs to be completed to show the product of the SN2 reaction. Here is a breakdown of components:

1. **Starting Molecule:**
   - A linear hydrocarbon chain with a bromine atom attached at the end. The bromine is depicted with a series of dashes and a wedge to indicate it is a stereocenter.

2. **Reaction Arrow:**
   - A vertical arrow points downward, showing the direction of the reaction from reactants to product.

3. **Product Box:**
   - Below the arrow is a blank space (dashed box) labeled "Drawing," where the reaction product is to be drawn.

**Reaction Mechanism:**
In an SN2 reaction, the nucleophile (NaSCH₃) attacks the electrophilic carbon atom to which the bromine is attached. This results in the inversion of stereochemistry at that carbon center, swapping the position of the bromine with the SCH₃ group in the product.

**Expected Outcome:**
The product should be drawn with the SCH₃ group replacing Br and using wedge and dash bonds to show the inversion of stereochemistry caused by the SN2 reaction mechanism.
Transcribed Image Text:**Title: Understanding the SN2 Reaction Mechanism** **Objective:** Draw the product of an SN2 reaction using the given reactants. Use wedge and dash bonds to indicate stereochemistry where appropriate. Inorganic byproducts should be ignored. **Reactants:** - The starting molecule is a bromide compound represented with a straight-chain hydrocarbon skeleton. - The bromine atom (Br) is attached to the terminal carbon of the chain with a wedge bond, indicating its stereochemistry. **Reagents:** - Sodium methanethiolate (NaSCH₃) - Tetrahydrofuran (THF) as the solvent **Diagram Explanation:** The diagram needs to be completed to show the product of the SN2 reaction. Here is a breakdown of components: 1. **Starting Molecule:** - A linear hydrocarbon chain with a bromine atom attached at the end. The bromine is depicted with a series of dashes and a wedge to indicate it is a stereocenter. 2. **Reaction Arrow:** - A vertical arrow points downward, showing the direction of the reaction from reactants to product. 3. **Product Box:** - Below the arrow is a blank space (dashed box) labeled "Drawing," where the reaction product is to be drawn. **Reaction Mechanism:** In an SN2 reaction, the nucleophile (NaSCH₃) attacks the electrophilic carbon atom to which the bromine is attached. This results in the inversion of stereochemistry at that carbon center, swapping the position of the bromine with the SCH₃ group in the product. **Expected Outcome:** The product should be drawn with the SCH₃ group replacing Br and using wedge and dash bonds to show the inversion of stereochemistry caused by the SN2 reaction mechanism.
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