Alpha cleavage

Alpha-cleavage (α-cleavage) in organic chemistry refers to the act of breaking the carbon-carbon bond^[1] adjacent to the carbon bearing a specified functional group.^[2]

Mass spectrometry

Generally this topic is discussed when covering tandem mass spectrometry fragmentation and occurs generally by the same mechanisms.^[3][4]

For example, of a mechanism of alpha-cleavage, an electron is knocked off an atom (usually by electron collision) to form a radical cation. Electron removal generally happens in the following order: 1) lone pair electrons, 2) pi bond electrons, 3) sigma bond electrons.

One of the lone pair electrons moves down to form a pi bond with an electron from an adjacent (alpha) bond. The other electron from the bond moves to an adjacent atom (not one adjacent to the lone pair atom) creating a radical. This creates a double bond adjacent to the lone pair atom (oxygen is a good example) and breaks/cleaves the bond from which the two electrons were removed.

Example of alpha cleavage

In molecules containing carbonyl groups, alpha-cleavage often competes with McLafferty rearrangement.

Photochemistry

In photochemistry, it is the homolytic cleavage of a bond adjacent to a specified group.^[4][5]

See also

• Inductive cleavage