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The functional group of alkenes is the carbon-carbon double bond. This double bond is responsible for the unsaturation in alkenes, making them more reactive than alkanes. Alkenes are commonly involved in addition reactions due to the presence of this functional group.
The functional group in lycopene is a series of conjugated double bonds, which are responsible for its characteristic red color and antioxidant properties.
is alkene's functional group. NOTE the double bond between the two carbon atoms.
The functional group in myrcene is an alkene group, which consists of a carbon-carbon double bond.
The prefix "cis-" is used in the name of a stereoisomer to indicate that the functional groups are on the same side of the double bond. This is in contrast to the prefix "trans-" which indicates that the functional groups are on opposite sides of the double bond.
The prefix "cis-" is used in the name of a stereoisomer to indicate that the functional groups are on the same side of the double bond.
Vinylic functional groups have a double bond directly attached to a carbon atom, while allylic functional groups have a double bond attached to a carbon atom that is next to a carbon-carbon double bond. This difference affects their reactivity and stability in organic reactions.
An ene-one molecule must have both an alkene (ene) and a ketone (one) functional group. The alkene functional group is characterized by a carbon-carbon double bond, while the ketone functional group consists of a carbon double-bonded to an oxygen and attached to two other carbon groups.
nitrogen base
A carbonyl group (C=O) is the functional group found in a ketone. It consists of a carbon atom double-bonded to an oxygen atom.