**Substitution Reaction Task****Objective:**Draw the product of the substitution reaction shown below. Ignore the inorganic byproducts.**Reaction Details:**- **Reactant Structure:** A linear alkyl chain with a bromine atom (Br) attached at the terminal position.- **Reagents Used:** - Sodium acetate (CH₃CO₂Na) - Dimethyl sulfoxide (DMSO)**Instructions:**The arrow indicates the transformation of the starting material to the product in the presence of sodium acetate and DMSO. Draw the resulting product of the substitution reaction, specifically focusing on the replacement of the bromine atom, which is expected to be substituted by the acetate group. **Note:**This reaction setup suggests an SN2 mechanism, where the nucleophile (acetate ion) displaces the leaving group (bromine) in one concerted step.

Given : structure of reactant. Tip : Sn2 reaction is occurring.

Answered: Draw the product of the substitution…

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Draw the product of the substitution reaction shown below. Ignore the inorganic byproducts.

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

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Question

**Substitution Reaction Task**

**Objective:**
Draw the product of the substitution reaction shown below. Ignore the inorganic byproducts.

**Reaction Details:**

- **Reactant Structure:**
A linear alkyl chain with a bromine atom (Br) attached at the terminal position.

- **Reagents Used:**
- Sodium acetate (CH₃CO₂Na)
- Dimethyl sulfoxide (DMSO)

**Instructions:**
The arrow indicates the transformation of the starting material to the product in the presence of sodium acetate and DMSO. Draw the resulting product of the substitution reaction, specifically focusing on the replacement of the bromine atom, which is expected to be substituted by the acetate group.

**Note:**
This reaction setup suggests an SN2 mechanism, where the nucleophile (acetate ion) displaces the leaving group (bromine) in one concerted step.

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