Elimination Reactions of Alkyl Halides

ELIMINATION REACTIONS
OF ALKYL HALIDES
Introduction
Elimination reactions of alkyl halides are important
reactions that compete with substitution reactions.
In an elimination reaction:
The fragments of some molecule (YZ) are removed
(eliminated) from adjacent atoms of the reactant
This elimination leads to the creation of a multiple bond
Dehydrohalogenation
Method for synthesizing alkenes : the elimination of HX
from adjacent atoms of an alkyl halide
Dehydrohalogenation
Dehydrohalogenation : The elements of a hydrogen

halide are eliminated from a haloalkane
as in SN1 and SN2 reactions, there is a leaving group and
an attacking Lewis base that possesses an electron pair
Dehydrohalogenation
Alpha () carbon atom : the carbon atom that bears the leaving
group (e.g., the halogen atom)
Beta () carbon atom : any carbon atom adjacent to alpha ()
carbon atom
hydrogen atom : a hydrogen atom attached to the carbon atom
Since the hydrogen atom that is eliminated in dehydrohalogenation
is from the carbon atom, these reactions are often called
eliminations. They are also often referred to as 1,2 eliminations.
Bases Used in Dehydrohalogenation
The conjugate base of an alcohol (an alkoxide: EtONa & t-
BuOK) prepared by treating an alcohol with an alkali metal
Sodium alkoxides : an alcohol react with sodium hydride

(NaH)
The E2 Reaction
The reaction rate depends on the concentration of isopropyl

bromide and the concentration of ethoxide ion : The reaction
must be bimolecular
Mechanism for the E2 Reaction
The E2 Reaction
In the E2 reaction the electron pair of the C-H bond pushes

the leaving group away from the opposite side as the base
removes the hydrogen.
The E1 Reaction
The formation of a tert-butyl cation as a common intermediate

the rate-determining step for both reactions unimolecular
SN2 versus E2
Relative steric hindrance in the substrate (class of alkyl

halide)
Temperature,
Size of the base/nucleophile (EtONa versus t-BuOK)
The effects of basicity and polarizability
SN2 versus E2 - Substrate
Primary Substrate
When the substrate is a primary halide and the base is
strong and unhindered, like ethoxide ion, substitution is
highly favored because the base can easily approach
the carbon bearing the leaving group
Secondary Substrate
With secondary halides, a strong base favors
elimination because steric hindrance in the substrate
makes substitution more difficult
Tertiary Substrate
With tertiary halides, steric hindrance in the substrate is severe and
an SN2 reaction cannot take place.
Elimination is highly favored, especially when the reaction is carried
out at higher temperatures.
Any substitution that occurs must take place through an SN1
mechanism
SN2 versus E2 - Temperature
Increasing the reaction temperature favors

elimination (E1 and E2) over substitution.
Elimination reactions have greater free energies
of activation than substitution reactions because
more bonding changes occur during elimination.
SN2 versus E2 - Size of the Base/Nucleophile
a strong sterically hindered base such as the tert-
butoxide ion influencing an elimination reaction of an
alkyl halide.
The relatively unhindered methoxide ion reacts with
octadecyl bromide primarily by substitution
The bulky tert-butoxide ion gives mainly elimination
SN2 versus E2 - Basicity and Polarizability
a weakly basic ion such as a
a strong, slightly polarizable
chloride ion (Cl-) or an
base such as hydroxide ion, acetate ion (CH3CO2-) or a
amide ion (NH2-), or alkoxide weakly basic and highly
ion (especially a hindered polarizable one such as Br-,
one) tends to increase the I-, or RS- increases the
likelihood of elimination likelihood of substitution
(E2). (SN2).
Tertiary Halides: SN1 versus E1
In most unimolecular reactions the SN1 reaction is favored

over the E1 reaction, especially at lower temperatures
If an elimination product is desired from a tertiary substrate,
it is advisable to use a strong base so as to encourage an
E2 mechanism over the competing E1 and SN1
mechanisms
Summary
Solved Problem
Give the product (or products) that you would expect to be

formed in each of the following reactions (i.e., would the
product be the only product, the major product, or a minor
product?).
Solved Problem
Solved Problem

Elimination Reactions of Alkyl Halides

Uploaded by

Copyright:

Available Formats

Elimination Reactions of Alkyl Halides

Uploaded by

Document Information

Original Description:

Original Title

Copyright

Available Formats

Share this document

Share or Embed Document

Sharing Options

Did you find this document useful?

Is this content inappropriate?

Copyright:

Available Formats

Elimination Reactions of Alkyl Halides

Uploaded by

Copyright:

Available Formats

ELIMINATION REACTIONS

Dehydrohalogenation : The elements of a hydrogen

Sodium alkoxides : an alcohol react with sodium hydride

The reaction rate depends on the concentration of isopropyl

In the E2 reaction the electron pair of the C-H bond pushes

The formation of a tert-butyl cation as a common intermediate

Relative steric hindrance in the substrate (class of alkyl

Increasing the reaction temperature favors

In most unimolecular reactions the SN1 reaction is favored

Give the product (or products) that you would expect to be

You might also like