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

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

Chemistry
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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**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.
Transcribed Image Text:**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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