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  2. Vinyl group - Wikipedia

    en.wikipedia.org/wiki/Vinyl_group

    On a carbon skeleton, sp 2-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 .)

  3. Vinyl cation - Wikipedia

    en.wikipedia.org/wiki/Vinyl_cation

    The vinyl cation is a carbocation with the positive charge on an alkene carbon. Its empirical formula of the parent ion is C 2 H + 3.Vinyl cation are invoked as reactive intermediates in solvolysis of vinyl halides, [1] [2] as well as electrophilic addition to alkynes and allenes.

  4. Allyl group - Wikipedia

    en.wikipedia.org/wiki/Allyl_group

    A site adjacent to the unsaturated carbon atom is called the allylic position or allylic site. A group attached at this site is sometimes described as allylic. Thus, CH 2 =CHCH 2 OH "has an allylic hydroxyl group". Allylic C−H bonds are about 15% weaker than the C−H bonds in ordinary sp 3 carbon centers and are thus more reactive.

  5. Vinylogy - Wikipedia

    en.wikipedia.org/wiki/Vinylogy

    The vinylogous enolate reacts at the terminal position of the double bond system (the γ-carbon), rather than the α-carbon immediately adjacent to the carbonyl, as would a simple enolate. Allylic electrophiles often react by vinylogous attack of a nucleophile rather than direct addition. Vinylogous aldol reaction. Cf. the simple aldol reaction.

  6. Vinyl - Wikipedia

    en.wikipedia.org/wiki/Vinyl

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  7. Vinylation - Wikipedia

    en.wikipedia.org/wiki/Vinylation

    In organic chemistry, vinylation is the process of attaching a vinyl group (CH 2 =CH−) to a substrate.Many organic compounds contain vinyl groups, so the process has attracted significant interest, especially since the reaction scope includes substituted vinyl groups.

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  9. Kumada coupling - Wikipedia

    en.wikipedia.org/wiki/Kumada_coupling

    In organic chemistry, the Kumada coupling is a type of cross coupling reaction, useful for generating carboncarbon bonds by the reaction of a Grignard reagent and an organic halide. The procedure uses transition metal catalysts, typically nickel or palladium, to couple a combination of two alkyl, aryl or vinyl groups.