'Dienes' are
hydrocarbons which contain two
double bonds. Dienes are intermediate between
alkenes and
polyenes.
Classes
Dienes can be divided into three classes:
#'Unconjugated dienes' have the double bonds separated by two or more single bonds.
#'Conjugated dienes' have
conjugated double bonds separated by one single bond. They are also the most stable.
#'Cumulated dienes' have the double bonds sharing a common atom as in a group of compounds called
allenes.
'Classes of Dienes' 1,5-Cyclooctadiene, an unconjugated diene. Notice that each double bond is two carbons away from the other. |  Isoprene, also known as 2-methyl-1,3-butadiene, is one of the simplest conjugated dienes. |  Propan-1,2-diene, also known as allene, is the simplest cumulated diene. |
In
organic chemistry a conjugated diene is also a
functional group. With a general formula of C
nH
n. a classic
organic reaction for the synthesis of dienes is the
Whiting reaction.
Reactions with dienes
The 1,3 configuration of double bonds found in 1,3-butadiene (conjugated double bonds) make these types of dienes capable of participating in more reaction types than is the case for
molecules with either just a single
alkene functional group or with multiple, but non-alternating, alkene groups. One possible reaction for such dienes is the
Diels-Alder reaction for example
Danishefsky’s diene.