A Mechanism for the Reduction Reaction
The Dissolving Metal Reduction of an Alkyne
CC CC
R
R
Li + R R CC
R
R
H
− H
NHEt
Radical anion Vinylic radical
A lithium atom donates an electron to
the π bond of the alkyne. An electron
pair shifts to one carbon as the
hybridization states change to sp^2.
The radical anion acts as
a base and removes a
proton from a molecule
of the ethylamine.
−
CC
R
R H H H
Li CC
R
R
CC
R
R
H NHEt H
Vinylic radical trans-Vinylic anion trans-Alkene
A second lithium atom
donates an electron to
the vinylic radical.
The anion acts as a base and
removes a proton from a second
molecule of ethylamine.
(^)
7.16 MOLECULAR FORMULAS OF HYDROCARBONS:
THE INDEX OF HYDROGEN DEFICIENCY
- 1-Hexene and cyclohexane have the same molecular formula (C 6 H 12 ):
CH 2 =CHCH 2 CH 2 CH 2 CH 3
1-Hexene Cyclohexane
1) Cyclohexane and 1-hexene are constitutional isomers.
- Alkynes and alkenes with two double bonds (alkadienes) have the general formula
CnH2n–2.
- Hydrocarbons with one triple bond and one double bond (alkenynes) and alkenes