ORGANIC CHEM. VOL.1+2-W/WILEYPLUS
ORGANIC CHEM. VOL.1+2-W/WILEYPLUS
12th Edition
ISBN: 9781119304241
Author: Solomons
Publisher: WILEY C
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Chapter 6, Problem 32P
Interpretation Introduction

Interpretation:

The reason behind the hydrolysis of methyl bromide taking place much faster in the presence of sodium iodide is to be explained.

Concept introduction:

The SN2 reaction is bimolecular nucleophilic substitution reaction, which means two components are involved in the rate determining step.

In the rate determining step, nucleophile approaches the carbon from the side directly opposite to the leaving group.

The SN2 reaction is a concerted reaction as bond formation and bond breaking occur in the same step.

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One of the steps in the mechanism of the above reaction as shown below. Draw the structure of all the products of this reaction. com/mm/takeAssignCourt Rotivity.do?locator assignment-take 1 pt ment Eto O Eto O 3. NaOH, H₂O, heat 4. HCI, H₂O, heat One of the steps in the mechanism of the above reaction is shown below. Draw the structure of all of the products of this reaction. O OEt O 1. Eto Na 2 Å OH You do not have to consider stereochemistry. • Draw enolate anions in their carbanion form. . You should include all products. Ôno P Ć [References) . Include counter-ions, e.g., Na, I, in your submission, but draw them in their own separate sketcher. . Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. . Separate multiple products using the + sign from the drop-down menu. ///-000- IF Previous Email Instructor
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