5.1
Alkene Nomenclature
Ethylene
5.2 Structure and Bonding in Alkenes
5.3 Isomerism in Alkenes
5.4 Naming Stereoisomeric Alkenes by the E-Z Notational System
5.5
Physical Properties of Alkenes
5.6 Relative Stabilities of Alkenes
5.7 Sources of Strain in Cycloalkenes
5.8
Preparation of Alkenes: Elimination Reactions
5.9 Dehydration of Alcohols
5.10 Regioselectivity in Alcohol Dehydration: The Zaitsev Rule
5.11 Stereoselectivity in Alcohol Dehydration
5.12 The Mechanism of Acid-Catalyzed Dehydration of Alcohols
5.13 Rearrangements in Alcohol Dehydration
5.14
Dehydrohalogenation of Alkyl Halides
5.15 Mechanism of the Dehydrohalogenation of Alkyl Halides: The E2
Mechanism
5.16 Anti Elimination in E2 Reactions: Stereoelectronic Effects
5.17 A Different Mechanism for Alkyl Halide Elimination: The E1
Mechanism
5.18 Summary
General review of eliminations to produce alkenes: view
LOCK
HAVEN (Chapter 7) and
ILLINOIS,
URBANA,
Discussions of
ELIMINATION
REACTIONS, along with example problems are
here.
Take the quizzes and bring questions to class.
At this
site
is a summary table of
SN1,
SN2, E1, and E2 REACTIONS.
A review of
ALKENE
NOMENCLATURE is provided at this
link.
Here
are demonstrations of
MARKOVNIKOV
and ANTI-MARKOVNIKOV additions that are three dimensional and
interactive. A downloadable movie showing
MARKOVNIKOV
additions is located
here.
Here
is an example of the
SN2
REACTION. The example is in Chime. Select the space filling
display for the best presentation. You can rotate the reacting system
as the reaction proceeds to see how it going!
For a nice overview of
SUBSTITUTION
AND ELIMINATION mechanism try this site.