Organic Chemistry-Package(Custom)
Organic Chemistry-Package(Custom)
4th Edition
ISBN: 9781259141089
Author: SMITH
Publisher: MCG
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Chapter 6, Problem 6.54P
Interpretation Introduction

(a)

Interpretation: The carbon radical which is formed by homolysis of the CHa bond in propylbenzene is to be identified. All reasonable resonance structures for the generated radical is to be drawn.

Concept introduction: The formation of carbocation, carbanion and free radical occur due to the heterolysis or homolysis process. Homolysis is opposite to the heterolysis. It forms radical with an unpaired electron.

Resonance is the delocalisation of π electrons in conjugated position which leads to the formation of more than one structure. These structures are known as resonance structures.

Interpretation Introduction

(b)

Interpretation: The carbon radical which is formed by homolysis of the CHb bond in propylbenzene is to be identified. All reasonable resonance structures for the generated radical is to be drawn.

Concept introduction: The formation of carbocation, carbanion and free radical occur due to the heterolysis or homolysis process. Homolysis is opposite to the heterolysis. It forms radical with an unpaired electron.

Resonance is the delocalisation of π electrons in conjugated position which leads to the formation of more than one structure. These structures are known as resonance structures.

Interpretation Introduction

(c)

Interpretation: The weaker CH bond is to be identified.

Concept introduction: The energy which is released or absorbed in the chemical reactions is referred to as bond dissociation energy. The strength of a bond in the reaction is determinedby bond dissociation energy. The chemical reactions in which energy is released from dissociation during the formation of products are known as exothermic reactions. In endothermic reactions, reactants absorb energy to form the desired products. Exothermic and endothermic reactions are opposite to each other. The value of ΔH° for exothermic and endothermic reactions is positive and negative respectively.

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Chapter 6 Solutions

Organic Chemistry-Package(Custom)

Ch. 6 - Prob. 6.11PCh. 6 - For a reaction with H=40kJ/mol, decide which of...Ch. 6 - For a reaction with H=20kJ/mol, decide which of...Ch. 6 - Draw an energy diagram for a reaction in which the...Ch. 6 - Prob. 6.15PCh. 6 - Prob. 6.16PCh. 6 - Problem 6.19 Consider the following energy...Ch. 6 - Draw an energy diagram for a two-step reaction,...Ch. 6 - Which value if any corresponds to a faster...Ch. 6 - Prob. 6.20PCh. 6 - Problem 6.23 For each rate equation, what effect...Ch. 6 - Prob. 6.22PCh. 6 - Identify the catalyst in each equation. a....Ch. 6 - Draw the products of homolysis or heterolysis of...Ch. 6 - Explain why the bond dissociation energy for bond...Ch. 6 - Classify each transformation as substitution,...Ch. 6 - Prob. 6.27PCh. 6 - Draw the products of each reaction by following...Ch. 6 - Prob. 6.29PCh. 6 - Prob. 6.30PCh. 6 - Prob. 6.31PCh. 6 - Prob. 6.32PCh. 6 - Prob. 6.33PCh. 6 - Prob. 6.34PCh. 6 - Prob. 6.35PCh. 6 - 6.39. a. Which value corresponds to a negative...Ch. 6 - Prob. 6.37PCh. 6 - At 25 C, the energy difference Go for the...Ch. 6 - For which of the following reaction is S a...Ch. 6 - Prob. 6.40PCh. 6 - Prob. 6.41PCh. 6 - 6.44 Consider the following reaction: . Use curved...Ch. 6 - Prob. 6.43PCh. 6 - Draw an energy diagram for the Bronsted-Lowry...Ch. 6 - Prob. 6.45PCh. 6 - Prob. 6.46PCh. 6 - Prob. 6.47PCh. 6 - Prob. 6.48PCh. 6 - The conversion of acetyl chloride to methyl...Ch. 6 - Prob. 6.50PCh. 6 - Prob. 6.51PCh. 6 - 6.54 Explain why is more acidic than , even...Ch. 6 - Prob. 6.53PCh. 6 - Prob. 6.54PCh. 6 - Prob. 6.55PCh. 6 - Although Keq of equation 1 in problem 6.57 does...Ch. 6 - Prob. 6.57P
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