For the given nitration reaction, orientation of the reaction has to be accounted. Concept Introduction: Activating and deactivating groups: The effect of substituents on the reaction rate of aromatic electrophilic substitution is given by activating or deactivating groups. Activating groups – ortho/para directing groups. The rate of reaction is increased by an activating groups (electron donating groups) relative to hydrogen. Deactivating groups – meta directing groups. The rate of reaction is decreased by a deactivating groups (electron withdrawing groups) relative to hydrogen.

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 ☐

Answer 1

Question

Chapter 22, Problem 22.28P

(a)

Interpretation Introduction

Interpretation:

For the given nitration reaction, orientation of the reaction has to be accounted.

Concept Introduction:

Activating and deactivating groups:

The effect of substituents on the reaction rate of aromatic electrophilic substitution is given by activating or deactivating groups.

Activating groups – ortho/para directing groups. The rate of reaction is increased by an activating groups (electron donating groups) relative to hydrogen.

Deactivating groups – meta directing groups. The rate of reaction is decreased by a deactivating groups (electron withdrawing groups) relative to hydrogen.

(b)

Interpretation Introduction

Interpretation:

For the given substitution reaction in step 2, reaction mechanism has to be proposed.

Concept Introduction:

Activating and deactivating groups:

The effect of substituents on the reaction rate of aromatic electrophilic substitution is given by activating or deactivating groups.

Activating groups – ortho/para directing groups. The rate of reaction is increased by an activating groups (electron donating groups) relative to hydrogen.

Deactivating groups – meta directing groups. The rate of reaction is decreased by a deactivating groups (electron withdrawing groups) relative to hydrogen.

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