ORGANIC CHEMISTRY GGC>CUSTOM<-TEXT
ORGANIC CHEMISTRY GGC>CUSTOM<-TEXT
2nd Edition
ISBN: 9781119288510
Author: Klein
Publisher: WILEY
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Chapter 9.3, Problem 5ATS

(a)

Interpretation Introduction

Interpretation:

Mechanism should be drawn for the given hydro halogenation reaction and needed to explain the product possibility.

Concept introduction:

  • Hydro halogenation reaction: In hydro halogenation reaction hydrogen halide added across the unsaturated bond (alkene). In this addition reaction chloride ion added to the most substituted carbon position of the alkene, which follows the Markovnikov’s rule.
  • Markovnikov’s rule: In addition reactions negatively addendum goes to most substituted carbon position in alkene.
  • Anti-Markovnikov’s product is possible if the carbocation is stabilized through strong electron donating group at less substituted carbon position.

To draw: the mechanism for given hydro halogenation reaction.

(b)

Interpretation Introduction

Interpretation:

Mechanism should be drawn for the given hydro halogenation reaction and needed to explain the product possibility.

Concept introduction:

  • Hydro halogenation reaction: In hydro halogenation reaction hydrogen halide added across the unsaturated bond (alkene). In this addition reaction chloride ion added to the most substituted carbon position of the alkene, which follows the Markovnikov’s rule.
  • Markovnikov’s rule: In addition reactions negatively addendum goes to most substituted carbon position in alkene.
  • Anti-Markovnikov’s product is possible if the carbocation is stabilized through strong electron donating group at less substituted carbon position.

To explain: The stability of the carbocation intermediate in reaction.

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Chapter 9 Solutions

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