Title: Ch' 11 Alkynes
1Ch. 11 Alkynes
2Structure and Bonding
3Structure and Bonding
4Naming Alkynes
1. The parent chain must contain the triple bond.
2. Change parent ending to -yne.
3. Give triple bond lowest possible .
6,6-dimethyl-2-heptyne
5What is the correct systematic name?
3-bromo-6-methyl-1-octyne
How many stereoisomers of this compound exist?
6Preparation of Alkynes
Alkynes can be prepared by double eliminations
geminal dihalide
vicinal dihalide
7Preparation of Alkynes
Examples-
8Reactions of Alkynes
Reactions of alkynes and alkenes are similar
can be E or Z
Breaking two p-bonds forms 4 new s-bonds
9Addition Reactions of Alkynes
1. Hydrogen halide addition (HCl, HBr, HI)-
produces geminal dihalides
Example-
geminal dihalide- two halogens located on the
same C atom
Mechanism?
10Addition Reactions of Alkynes
Another example-
Addition follows Markovnikovs rule
11Addition Reactions of Alkynes
2. Halogenation (Cl2, Br2) produces tetrahalides
Examples-
12(No Transcript)
13Addition Reactions of Alkynes
3. H2O Addition produces ketones
Hg2 increases rate, but is not
required Markovnikovs rule is followed
14Addition Reactions of Alkynes
Mechanism is similar to alkene hydration Enol is
produced, tautomerizes to ketone
Enol form (less stable)
Keto form (more stable)
Tautomers constitutional isomers differing in
the placement of a double bond and a hydrogen
atom that are in equilibrium with one another
15Addition Reactions of Alkynes
4. Hydroboration-oxidation conversion of
alkynes to carbonyl compounds (aldhydes or
ketones)
Mechanism is similar to alkene hydroboration Term
inal alkynes produce aldehydes (anti-Markovnikov
addition) Enol is formed and undergoes
tautomerization
16III. Hydration of alkynes
17(No Transcript)
18(No Transcript)
19(No Transcript)
20Reactions of Acetylide Anions
Terminal alkynes can be deprotonated to
produce strong nucleophiles
acetylide anion
NaNH2 and NaH are typical bases
21Reactions of Acetylide Anions
The acetylide ions formed may be used as
nucleophiles in SN2 reactions
Example-
Would this one work?
22Reactions of Acetylide Anions
The acetylide ions formed may be used as
nucleophiles in SN2 reactions
23Reactions of Acetylide Anions
2. Reaction with Epoxides strong nucleophile
reacts by SN2 pathway
Why does the attack occur at the top carbon
rather than the bottom one?
24Organic Synthesis
Many complex molecules require multiple steps to
prepare
Tamiflu
25Organic Synthesis
To work synthesis problems, you must- 1)
Understand the reactions 2) Be able to arrange
them in the correct order
26Organic Synthesis
How could this compound be synthesized
from acetylene?
27Organic Synthesis
How could this synthesis be carried out?
28(No Transcript)