ORGANIC CHEMISTRY-ETEXT REG ACCESS
ORGANIC CHEMISTRY-ETEXT REG ACCESS
12th Edition
ISBN: 9781119308362
Author: Solomons
Publisher: WILEY
Question
Book Icon
Chapter 10, Problem 39P
Interpretation Introduction

Interpretation:

The reason for the enhance rate of substitution at C5 in 2,2 dimethyl hexane is to be explained.

Concept Introduction:

The breaking of a covalent bond in a way that each atom takes one electron from the shared pair is called homolytic fission.

Homolytic fission results in the formation of a radical, and the order of stability of the radical is as follows:

1o<2o<3o

Free radical halogenation is a reaction that substitutes a chlorine for a hydrogen on an alkane. This reaction is a photochemical one. That is, it occurs only when performed in the presence of uv light

Free radical reactions are described in three steps: initiation steps, propagation steps, and termination steps

Blurred answer
Students have asked these similar questions
Use the Hammond postulate to explain why (CH3)2C = CH2 reacts faster than CH3CH = CH2 in electrophilic addition of HX.
Are there any types of C-C bond that can be formed from a Friedel-Crafts reaction other than through alkylation? What other kinds of functional groups would they be if so?
1. b) Show the MECHANISM for the POLAR addition of molecular chlorine to cyclopentane. c) The reaction of toluene and ethylbenzene was through the alkyl groups, -CH 3 and -CH 2 CH 3, respectively. Why didn’t xylene, which has TWO methyl groups, react with bromine in the time allotted?
Knowledge Booster
Background pattern image
Similar questions
SEE MORE QUESTIONS
Recommended textbooks for you
Text book image
Organic Chemistry: A Guided Inquiry
Chemistry
ISBN:9780618974122
Author:Andrei Straumanis
Publisher:Cengage Learning
Text book image
Organic Chemistry
Chemistry
ISBN:9781305580350
Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Publisher:Cengage Learning