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In chemistry, vinyl or ethenyl is the functional group −CH=CH2, namely the ethylene molecule (H2C=CH2) minus one hydrogen atom. The name is also used for any compound containing that group, namely R−CH=CH2 where R is any other group of atoms.
Vinyl is one of the alkenyl functional groups. On a carbon skeleton, sp2-hybridized carbons or positions are often called vinylic. Allyls, acrylates and styrenics contain vinyl groups. (A styrenic crosslinker with two vinyl groups is called divinyl benzene.)
Vinyl groups can polymerize with the aid of a radical initiator or a catalyst, forming vinyl polymers. In these polymers, the double bonds of the vinyl monomers turn into single bonds and the different monomers are joined by single bonds. Vinyl groups do not exist in vinyl polymer; the term refers to the precursor. It is sometimes important to ascertain the absence of unreacted vinyl monomer in the final product when the monomer is toxic or reduces the performance of the plastic. The following table gives some examples of vinyl polymers.
|Monomer example||Example of resulting polymer|
|Vinyl chloride||Polyvinyl chloride (PVC)|
|Vinyl fluoride||Polyvinyl fluoride (PVF)|
|Vinyl acetate||Polyvinyl acetate (PVAc)|
- In allyl compounds, where the next carbon is saturated but substituted once, allylic rearrangement and related reactions are observed.
- Allyl Grignard reagents can attack with the vinyl end first.
- If next to an electron-withdrawing group, conjugate addition (Michael addition) occurs.
Vinyl organometallics, e.g. vinyl lithium, participate in coupling reactions such as in Negishi coupling.
- IUPAC Provisional Recommendations 2004 Chapter 5