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  2. Acyl group - Wikipedia

    en.wikipedia.org/wiki/Acyl_group

    The acyls are between the hydrocarbyls and the carboxylic acids. The hydrocarbyl group names that end in -yl are not acyl groups, but alkyl groups derived from alkanes (methyl, ethyl, propyl, butyl), alkenyl groups derived from alkenes (propenyl, butenyl), or aryl groups .

  3. Alkyl group - Wikipedia

    en.wikipedia.org/wiki/Alkyl_group

    Alkyl groups that contain one ring have the formula −C n H 2n−1, e.g. cyclopropyl and cyclohexyl. The formula of alkyl radicals are the same as alkyl groups, except the free valence "−" is replaced by the dot "•" and adding "radical" to the name of the alkyl group (e.g. methyl radical •CH 3).

  4. Plasmalogen - Wikipedia

    en.wikipedia.org/wiki/Plasmalogen

    Glycerophospholipids of biochemical relevance are divided into three subclasses based on the substitution present at the sn-1 position of the glycerol backbone: acyl, alkyl and alkenyl. [4] Of these, the alkyl and alkenyl moiety in each case form an ether bond, which makes for two types of ether phospholipids , plasmanyl (alkyl moiety at sn-1 ...

  5. Acetyl group - Wikipedia

    en.wikipedia.org/wiki/Acetyl_group

    The carbonyl center of an acyl radical has one non-bonded electron with which it forms a chemical bond to the remainder (denoted with the letter R) of the molecule. The acetyl moiety is a component of many organic compounds , including acetic acid , the neurotransmitter acetylcholine , acetyl-CoA , acetylcysteine , acetaminophen (also known as ...

  6. Acyl halide - Wikipedia

    en.wikipedia.org/wiki/Acyl_halide

    Acyl halides are rather reactive compounds often synthesized to be used as intermediates in the synthesis of other organic compounds. For example, an acyl halide can react with: water, to form a carboxylic acid. This hydrolysis is the most heavily exploited reaction for acyl halides as it occurs in the industrial synthesis of acetic acid.

  7. Allyl group - Wikipedia

    en.wikipedia.org/wiki/Allyl_group

    Structure of the allyl group. In organic chemistry, an allyl group is a substituent with the structural formula −CH 2 −HC=CH 2.It consists of a methylene bridge (−CH 2 −) attached to a vinyl group (−CH=CH 2).

  8. Acylation - Wikipedia

    en.wikipedia.org/wiki/Acylation

    In chemistry, acylation is a broad class of chemical reactions in which an acyl group (R−C=O) is added to a substrate. The compound providing the acyl group is called the acylating agent. The substrate to be acylated and the product include the following: alcohols, esters; amines, amides; arenes or alkenes, [1] ketones

  9. α,β-Unsaturated carbonyl compound - Wikipedia

    en.wikipedia.org/wiki/Α,β-Unsaturated_carbonyl...

    α,β-Unsaturated carbonyl compounds featuring a carbonyl conjugated to an alkene that is terminal, or vinylic, contain the acryloyl group (H 2 C=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 ...