Scribd
Upload
15 views6 pages

Chapter 8 Alkenes

Uploaded by

forschooldocuments2004
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
Available Formats
Download as PDF, TXT or read online on Scribd
15 views6 pages

Chapter 8 Alkenes

Uploaded by

forschooldocuments2004
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
Available Formats
Download as PDF, TXT or read online on Scribd
You are on page 1/ 6

Chapter 8

Addition Reactions

*A variety reagents will react with alkenes to provide products


from addition reactions.

(1)

Hydrogenation, Section 8.1

*Hydrogen adds across alkenes and this can provide alkanes.


This chemistry is usually done in the presence of a transition
metal catalyst. Both hydrogen atoms add to the same side of the
double bond (this is called syn addition).

(2)

*When a substance has C-C double bonds, it is called an


unsaturated compound. With addition of hydrogen, it becomes a
saturated compound (i.e., it is saturated with hydrogen).

(3)

*D gas may be used to incorporate the hydrogen isotope.


2

(4)

*With plant oils (triglycerides), polyunsaturated fats have


multiple C-C double bonds. Reaction with hydrogen converts
the oils to saturated fats.
*As described in the previous chapter, hydrogenation of
isomeric alkenes provides a means of estimating alkene
stabilities. The more stable structures release less heat upon
hydrogenation.

(5)

Hydrohalogenation, section 8.4

*HCl and HBr will add to an alkene to provide an alkyl halide.


H
(6) #I

*This is a two-step reaction involving:


1. Transfer of the proton to the alkene, forming a
carbocation.
2. Nucleophilic halide attack at the carbocation

~
Brt) Attack

~
=Br
: cuis At ether

(7) 3 Side of carbuncation

*The proton is an electrophile, or electronic seeking/loving


species.

*For unsymmetrical alkenes, the reaction always goes through


the more highly substituted carbocation. This is called the
Markovnikov’ rule.

(8)
#
Hi

Location ~itOct
*When a chirality center is formed, both enantiomers are
typically generated.
ch3mistry
Follows

(9) m Rule
.

Hydration, section 8.6

*Water will also add to alkenes to provide alcohols. The


chemistry is acid-catalyzed and it follows Markovnikov’s rule.
Similar mechanism to hydrohalogenation.
Withexcept
#EAs a
·

ou

(10)
WithHo My t
·

H He

*Again, both enantiomers are formed if a chirality center is


generated due to planar carbocation.

(11) ↓ - UniFinished
*This chemistry is the reverse of alcohol dehydration.

*The water addition can be favored by use of an excess of water.

*A similar addition reaction is possible with alcohol additions to


alkenes.
* Always go for most stable CATALYSIS

o
CH]

(12) Like
i
F

Hydroboration, section 8.8,9

*Boron hydrides will add across alkene double bonds to give


alkyl boranes. The hydrogen is more electronegative than the
boron, so the boron is the electrophile. With three reactive B-H
bonds, three alkenes may add.
= HO
(13)7
B
=

ou

*In a second step, the carbon-boron bond is oxidatively cleaved


to provide an alcohol. Note that this provides an “anti-
Markovnikov” addition type of addition product (different from
acid-catalyzed hydration of alkenes.

(14)

*The addition of boron hydride occurs in a syn manner, which is


evident with product formation.
Compart
(15)
E
Halogenation, section 8.10

*Br and Cl add across alkenes to give 1,2-dihalide products.


2 2

The addition occurs in an anti manner (opposite sides of double


bond).

(16) t
Why ANTI ?
"I

of Halonium ION
Ring-opening

*The anti addition occurs due to the formation of a halonium ion


intermediate. Ring opening of the halonium ion occurs by
nucleophilic attack from the backside of the bond orbital – much
like the Sn2 transformation. With backside attack (and inversion
of the carbon) the anti-addition product is formed.

(17)

*The stereochemistry of the alkene is retained in the product.

(18)
*More highly substituted alkenes tend to react faster. This is due
to higher electron density in the double bond (remember, alkyl
groups are electron donating).

(19)

*If water or alcohols are introduced in the mixture, the water or


alcohol can act as the nucleophiles and the halohydrin (or ether)
is formed.

(20)

*When unsymmetrical alkenes react, the halonium ion deposits


positive charge on the highly substituted carbon. Thus,
nucleophilic attack tends to occur at the more highly substituted
position.

(21)

Epoxides, section 8.11

*Peroxy acids react with alkenes to give epoxides. The most


common reagent is meta-chloroperoxy benzoic acid (MCPBA).
(22)

*Alkene stereochemistry is also retained in this reaction.


Insertion of the oxygen atom occurs in one step.

(23)

*Epoxides may also be prepared by intramolecular reactions of


halohydrins.

(24)

Ozonolysis, Section 8.12

*When alkenes react with ozone, O , the ozone essentially


3

inserts into the double bond and reaction with a reducing agent
(dimethyl sulfide or Zn, HCl) provides two carbonyl “halves.”

(25)

*This can also lead to ring opening.

(26)

You might also like