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HO' NaOH acetonitrile Br

HO' NaOH acetonitrile Br

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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**Question 8 of 28** **Title:** SN2 Reaction Product **Instructions:** Draw the product of the SN2 reaction shown below. Ignore inorganic byproducts. **Reaction Details:** - **Reactant Structure:** A linear chain with a hydroxyl group (HO) on the left end and a bromine atom (Br) on the right end. - **Reagents:** - NaOH - Acetonitrile **Diagram Details:** There's an arrow pointing downward beneath the reactants and reagents, indicating the direction of the reaction. Below the arrow, there's a red dashed box labeled "Drawing" for where the product should be illustrated. **Guidance:** Recognize the SN2 mechanism involves a backside attack by the nucleophile, leading to the substitution of the bromine atom with the nucleophile. Consider drawing the expected product within the space provided.
Transcribed Image Text:**Question 8 of 28** **Title:** SN2 Reaction Product **Instructions:** Draw the product of the SN2 reaction shown below. Ignore inorganic byproducts. **Reaction Details:** - **Reactant Structure:** A linear chain with a hydroxyl group (HO) on the left end and a bromine atom (Br) on the right end. - **Reagents:** - NaOH - Acetonitrile **Diagram Details:** There's an arrow pointing downward beneath the reactants and reagents, indicating the direction of the reaction. Below the arrow, there's a red dashed box labeled "Drawing" for where the product should be illustrated. **Guidance:** Recognize the SN2 mechanism involves a backside attack by the nucleophile, leading to the substitution of the bromine atom with the nucleophile. Consider drawing the expected product within the space provided.
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