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In organic chemistry, the acryloyl group is form of enone with structure H2C=CH–C(=O)–; it is the acyl group derived from acrylic acid. The preferred IUPAC name for the group is prop-2-enoyl, and it is also known as acrylyl or simply (and incorrectly) as acryl. Compounds containing an acryloyl group can be referred to as "acrylic compounds".
An acrylic compound is typically an α,β-unsaturated carbonyl compound: it contains a carbon–carbon double bond and a carbon–oxygen double bond (carbonyl) separated by a carbon–carbon single bond, thus possessing properties characteristic for both functional groups :
- at the C=C bond: electrophilic addition of acids and halogens, hydrogenation, hydroxylation and cleavage of the bond
- at the C=O bond: nucleophilic substitution (such as in esters) or nucleophilic addition (such as in ketones). The carboxyl group of acrylic acid can react with ammonia to form acrylamide, or with an alcohol to form an acrylate ester.
In addition, since both double bonds are separated by a single C–C bond, the double bonds are conjugated.
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