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  2. 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.

  3. Carbocation - Wikipedia

    en.wikipedia.org/wiki/Carbocation

    5, acylium ions RCO +, and vinyl C 2 H + 3 cations. [2] Until the early 1970s, carbocations were called carbonium ions. [3] In the present-day definition given by the IUPAC, a carbocation is any even-electron cation with significant partial positive charge on a carbon atom.

  4. Vinyl neodecanoate - Wikipedia

    en.wikipedia.org/wiki/Vinyl_neodecanoate

    Vinyl neodecanoate (trade name VeoVa 10) is a vinylic monomer that is virtually always used in combination with other monomers to create latices or emulsion polymers. [3] The trade name is an acronym of Vinyl ester of Versatic Acid with the number 10 meaning 10 carbons in the molecule. It has a medium to low glass transition temperature of -3 °C.

  5. Vinylene carbonate - Wikipedia

    en.wikipedia.org/wiki/Vinylene_carbonate

    Since its first description in 1953, [3] ethylene carbonate has been commonly used as starting material for vinylene carbonate. In the first stage, monochlorethylene carbonate is produced in a UV-initiated photochlorination reaction with chlorine or sulfuryl chloride at 60-70 °C in bulk.

  6. Carbenium ion - Wikipedia

    en.wikipedia.org/wiki/Carbenium_ion

    Strongly basic nucleophiles, especially hindered ones, favor elimination over addition. Because even weak nucleophiles will react with carbocations, most can only be directly observed or isolated in non-nucleophilic media like superacids. [6] Relative formation energy of carbocations from computational calculation

  7. Vinylacetylene - Wikipedia

    en.wikipedia.org/wiki/Vinylacetylene

    At one time, chloroprene (2-chloro-1,3-butadiene), an industrially important monomer, was produced via the intermediacy of vinyl acetylene. [7] In this process, acetylene is dimerized to give vinyl acetylene, which is then combined with hydrogen chloride to give 4-chloro-1,2-butadiene via 1,4-addition.

  8. Polyvinylidene fluoride - Wikipedia

    en.wikipedia.org/wiki/Polyvinylidene_fluoride

    It is available in the form of piping products, sheet, tubing, films, plate and an insulator for premium wire. It can be injected, molded or welded and is commonly used in the chemical, semiconductor, medical and defense industries, as well as in lithium-ion batteries.

  9. Category:Carbocations - Wikipedia

    en.wikipedia.org/wiki/Category:Carbocations

    Pages in category "Carbocations" ... Vinyl cation This page was last edited on 31 December 2018, at 21:47 (UTC). Text is available under the Creative ...