The reaction of sodium phenoxide with iodomethane yields anisole. What kind of reaction is taking place in this conversion is to be stated. A mechanism for the conversion is to be proposed. Concept introduction: Phenoxide ion is nucleophilic. When it is treated with alkyl iodides a bimolecular nucleophilic displacement (SN 2 ) reaction will occur. Iodine is removed and phenoxy group gets attached to methyl group. To state: The kind of reaction that occurs when phenoxide ion is treated with iodomethane to produce anisole is to be stated. A mechanism for this reaction is also to be proposed. To propose: A mechanism for this conversion.

Question

You are trying to decide if there is a single reagent you can add that will make the following synthesis possible without any other major side products: xi 1. ☑ 2. H₂O хе i Draw the missing reagent X you think will make this synthesis work in the drawing area below. If there is no reagent that will make your desired product in good yield or without complications, just check the box under the drawing area and leave it blank. Click and drag to start drawing a structure. There is no reagent that will make this synthesis work without complications. : ☐ S ☐

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Chapter 17.SE, Problem 77AP

Interpretation Introduction

Interpretation:

The reaction of sodium phenoxide with iodomethane yields anisole. What kind of reaction is taking place in this conversion is to be stated. A mechanism for the conversion is to be proposed.

Concept introduction:

Phenoxide ion is nucleophilic. When it is treated with alkyl iodides a bimolecular nucleophilic displacement (SN²) reaction will occur. Iodine is removed and phenoxy group gets attached to methyl group.

To state:

The kind of reaction that occurs when phenoxide ion is treated with iodomethane to produce anisole is to be stated. A mechanism for this reaction is also to be proposed.

To propose:

A mechanism for this conversion.

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