ORGANIC CHEMISTRY-OWL V2 ACCESS
ORGANIC CHEMISTRY-OWL V2 ACCESS
8th Edition
ISBN: 9781305582422
Author: Brown
Publisher: CENGAGE L
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Chapter 22, Problem 22.14P

(a)

Interpretation Introduction

Interpretation:

Resonance contributor for the cation formed during electrophilic aromatic substitution has to be given for the given ortho-para directing -OH group.

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:

Resonance contributor for the cation formed during electrophilic aromatic substitution has to be given for the given ortho-para directing -OC(O)CH3 group.

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.

(c)

Interpretation Introduction

Interpretation:

Resonance contributor for the cation formed during electrophilic aromatic substitution has to be given for the given ortho-para directing -N(CH3)2 group.

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.

(d)

Interpretation Introduction

Interpretation:

Resonance contributor for the cation formed during electrophilic aromatic substitution has to be given for the given ortho-para directing -NHC(O)CH3 group.

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.

(e)

Interpretation Introduction

Interpretation:

Resonance contributor for the cation formed during electrophilic aromatic substitution has to be given for the given ortho-para directing phenyl group.

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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Chapter 22 Solutions

ORGANIC CHEMISTRY-OWL V2 ACCESS

Ch. 22 - What product do you predict from the reaction of...Ch. 22 - Other groups besides H+ can act as leaving groups...Ch. 22 - Prob. 22.14PCh. 22 - Prob. 22.15PCh. 22 - Prob. 22.16PCh. 22 - Prob. 22.17PCh. 22 - Suggest a reason why the nitroso group, N=O, is...Ch. 22 - Prob. 22.19PCh. 22 - Prob. 22.20PCh. 22 - The following molecules each contain two aromatic...Ch. 22 - Prob. 22.22PCh. 22 - Prob. 22.23PCh. 22 - The insecticide DDT is prepared by the following...Ch. 22 - Prob. 22.25PCh. 22 - Prob. 22.26PCh. 22 - Prob. 22.27PCh. 22 - Prob. 22.28PCh. 22 - Prob. 22.29PCh. 22 - Prob. 22.32PCh. 22 - Show how to prepare each compound from...Ch. 22 - Prob. 22.34PCh. 22 - Show reagents and conditions to bring about the...Ch. 22 - Prob. 22.36PCh. 22 - Propose a synthesis for each compound from...Ch. 22 - The first widely used herbicide for the control of...Ch. 22 - The first widely used herbicide for the control of...Ch. 22 - Prob. 22.40PCh. 22 - Prob. 22.41PCh. 22 - Prob. 22.42PCh. 22 - Prob. 22.43PCh. 22 - Cancer of the prostate is the second leading cause...Ch. 22 - Prob. 22.45PCh. 22 - Prob. 22.46PCh. 22 - Prob. 22.47PCh. 22 - When certain aromatic compounds are treated with...Ch. 22 - Prob. 22.49PCh. 22 - Following is the structure of miconazole, the...Ch. 22 - Prob. 22.51PCh. 22 - Prob. 22.52PCh. 22 - Prob. 22.53PCh. 22 - Show how the antidepressant venlafaxine (Effexor)...Ch. 22 - Prob. 22.57PCh. 22 - Given this retrosynthetic analysis, propose a...Ch. 22 - Prob. 22.59PCh. 22 - Prob. 22.60PCh. 22 - Prob. 22.61PCh. 22 - A newer generation of antipsychotics, among them...Ch. 22 - Prob. 22.63P
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