15.S: Alkenes - Reactions and Synthesis (Summary)

Last updated
Save as PDF

Page ID: 452175

\( \newcommand{\vecs}[1]{\overset { \scriptstyle \rightharpoonup} {\mathbf{#1}} } \) \( \newcommand{\vecd}[1]{\overset{-\!-\!\rightharpoonup}{\vphantom{a}\smash {#1}}} \)\(\newcommand{\id}{\mathrm{id}}\) \( \newcommand{\Span}{\mathrm{span}}\) \( \newcommand{\kernel}{\mathrm{null}\,}\) \( \newcommand{\range}{\mathrm{range}\,}\) \( \newcommand{\RealPart}{\mathrm{Re}}\) \( \newcommand{\ImaginaryPart}{\mathrm{Im}}\) \( \newcommand{\Argument}{\mathrm{Arg}}\) \( \newcommand{\norm}[1]{\| #1 \|}\) \( \newcommand{\inner}[2]{\langle #1, #2 \rangle}\) \( \newcommand{\Span}{\mathrm{span}}\) \(\newcommand{\id}{\mathrm{id}}\) \( \newcommand{\Span}{\mathrm{span}}\) \( \newcommand{\kernel}{\mathrm{null}\,}\) \( \newcommand{\range}{\mathrm{range}\,}\) \( \newcommand{\RealPart}{\mathrm{Re}}\) \( \newcommand{\ImaginaryPart}{\mathrm{Im}}\) \( \newcommand{\Argument}{\mathrm{Arg}}\) \( \newcommand{\norm}[1]{\| #1 \|}\) \( \newcommand{\inner}[2]{\langle #1, #2 \rangle}\) \( \newcommand{\Span}{\mathrm{span}}\)\(\newcommand{\AA}{\unicode[.8,0]{x212B}}\)

Concepts & Vocabulary

8.1 Preparing Alkenes: A Preview of Elimination Reactions (CHM 223)

Alkenes can be prepared by either E1 or E2 elimination reactions of alkyl halides.

8.2 Halogenation of Alkenes: Addition of X₂

Halogen molecules can react as electrophiles due to polarization of the halogen-halogen bond.
During electrophilic addition of halogens to pi bonds, an intermediate halonium ion is formed.
During electrophilic halogenation, ring opening of the halonium intermediate causes anti stereochemistry of the halogen atoms in the dihalide product.

8.3 Halohydrins from Alkenes: Addition of HOX

Halohydrins have a halogen and a hydroxide on adjacent carbon atoms. Bromohydrin and chlorohydrin are the specific types of halohydrins where the halogen is bromine or chlorine respectively.
In halohydrin formation a carbocation intermediate is formed on the more substituted carbon (when available). This causes the hydroxide to be added to the more substituted carbon of the original alkene and the halogen to add to the less substituted carbon.

8.4 Hydration of Alkenes: Addition of H₂O by Oxymercuration

Electrophilic hydration is the addition of water to an alkene with one carbon adding a hydrogen and the other carbon a hydroxide.
The mechanism begins with addition of a proton, yielding the more substituted carbocation.
Carbocations can undergo hydride shifts and alkyl shifts to form a more stable carbocation when possible.
Markovnikov addition through acid and water or oxymercuration-demercuration yields the more substituted alcohol product (when the two sides of the alkene are not equally substituted).
Oxymercuration-demercuration avoids carbocation rearrangements through mercurinium ion bridge.

8.5 Hydration of Alkenes: Addition of H₂O by Hydroboration

Hydroboration-oxidation proceeds through anti-Markovnikov addition of water to an alkene, yielding the less substituted alcohol.

8.6 Reduction of Alkenes: Hydrogenation

Hydrogenation reactions increase the number of carbon-hydrogen bonds, therefore are reduction reactions.
Addition of hydrogen to carbon-carbon pi bonds is called hydrogenation.
Hydrogenation requires a catalyst to lower the activation energy allowing the reaction to proceed (commonly nickel, palladium or platinum).
Hydrogenation reactions occur primarily with syn addition of the two hydrogen atoms, though potential for isomerization makes this uncertain.

8.7 Oxidation of Alkenes: Epoxidation and Hydroxylation

Epoxidation can be carried out by reacting an alkene with a peroxy acid such as MCPBA.
Anti dihydroxylation is achieved by ring opening an epoxide with water under acidic or basic conditions.
Vicinal diols have hydroxy groups on adjacent carbon atoms.
Syn dihydroxylation occurs through reaction with osmium tetraoxide, followed by reduction of the intermediate with sulfur compounds.

8.8 Oxidation of Alkenes: Cleavage to Carbonyl Compounds (CHM 223)

Ozonolysis is the cleavage of an alkene resulting in carbonyls at each carbon of the alkene.
Alkenes can be cleaved by potassium permanganate, which also results in carbonyls at each alkene carbon, though potassium permanganate will oxidize every carbon-hydrogen bonds on the alkene to a carbon-oxygen bond.

8.9 Addition of Carbenes to Alkenes: Cyclopropane Synthesis (CHM 321)

Organic molecules that have a carbon with only two bonds and a lone pair of electrons are called carbenes.
Most carbenes are highly reactive and short-lived and are often created in situ.
Carbenes can be formed from diazo compounds by reacting wtih a copper catalyst.
Carbenes will react with alkenes to form cyclopropane rings.

8.10 Radical Addition to Alkenes: Chain-Growth Polymers (reference only)

Monomers are units that repeat to form a polymer.
In radical polymerization, the polymer chain reaction is initiated by a radical.
Polymer chain reactions occur through a series of steps beginning with initiation, continuing through propagation, and ending in termination.

8.11 Biological Additions of Radicals to Alkenes (reference only)

8.12 Reaction Stereochemistry: Addition of H₂O to an Achiral Alkene

Since addition of water to an alkene proceeds through a planar carbocation intermediate, achiral alkenes lead to a racemic mixture of alcohol products.

8.13 Reaction Stereochemistry: Additon of H₂O to a Chiral Alkene

Addition of water to alkenes which also contain a stereocenter does not lead to a 50:50 mixture of R and S products as the chiral center can reduce reactivity from one side of the carbocation. The products of this type of reaction will be diastereomers, since the original stereocenter will not change and the product will have an additional stereocenter.

Skills to Master

Skill 15.1 Draw accurate Electrophilic Addition Mechanisms incorporating halonium intermediates.
Skill 15.2 Draw accurate Electrophilic Addition Mechanisms incorporating carbocation intermediates.
Skill 15.3 Draw Markovnikov products of alkene additions based on the most substituted carbocation intermediate.
Skill 15.4 Draw hydrogenation products of alkenes.
Skill 15.5 Draw appropriate epoxidation products including sterechemistry.
Skill 15.6 Describe how to prepare syn and anti diols from alkenes.