Essential Organic Chemistry Study Guide & Solution Manual, Books a la Carte Edition
Essential Organic Chemistry Study Guide & Solution Manual, Books a la Carte Edition
3rd Edition
ISBN: 9780134255644
Author: Bruice, Paula Yurkanis
Publisher: PEARSON
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Chapter 14, Problem 16P

(a)

Interpretation Introduction

Interpretation:

Preparation of 2-bromo-2-methyl from 2-methylpropane has to be shown.

Concept Introduction:

Radical or free radical: The unpaired valence electron of an atom, molecule, or ion is called as radical.

In a halogenation reaction, one or more halogen atoms are introduced into an organic compound. Generally, these reactions are initiated in the presence of light or heat.

Bromination:

Essential Organic Chemistry Study Guide & Solution Manual, Books a la Carte Edition, Chapter 14, Problem 16P , additional homework tip  1

(b)

Interpretation Introduction

Interpretation:

Preparation of 2-methyl-1- propene from 2-methylpropane has to be shown.

Concept Introduction:

Radical or free radical: unpaired valence electron of an atom, molecule, or ion is called as radical.

In a halogenation reaction, one or more halogen atoms are introduced into an organic compound. Generally, these reactions are initiated in the presence of light or heat.

Bromination:

Essential Organic Chemistry Study Guide & Solution Manual, Books a la Carte Edition, Chapter 14, Problem 16P , additional homework tip  2

(c)

Interpretation Introduction

Interpretation:

Preparation of 2-Iodo-2-methylpropane form 2-methylpropane has to be shown.

Concept Introduction:

Radical or free radical: unpaired valence electron of an atom, molecule, or ion is called as radical.

In a halogenation reaction, one or more halogen atoms are introduced into an organic compound. Generally, these reactions are initiated in the presence of light or heat.

Bromination:

Essential Organic Chemistry Study Guide & Solution Manual, Books a la Carte Edition, Chapter 14, Problem 16P , additional homework tip  3

Markovnikov’s rule:

Alkene undergoes hydro halogenation using hydrogen halide through breaking of carbon to carbon double bond, followed by the electrophilic addition of a hydrogen atom and halogen. The halide ion will add to the more substituted carbon in the alkene.

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