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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.
However, reactions that would require the formation of unstable carbocations (methyl, vinyl, aryl or primary carbon) proceed via S N 2 mechanism. The hydrohalic acid also plays an important role, as the rate of reaction is greater with hydroiodic acid than with hydrobromic acid. Hydrochloric acid only reacts under more rigorous conditions.
A carbocation is an ion with a positively charged carbon atom. Among the simplest examples are the methenium CH + 3, methanium CH + 5, acylium ions RCO +, and vinyl C 2 H + 3 cations. [2] Until the early 1970s, carbocations were called carbonium ions. [3]
This forms a carbocation intermediate, and the X then bonds to the positive carbon that is available, as in the following two-step reaction. [4] CH 2 CH 2 + HX → CH 2 CH + 3 + X − CH 2 CH + 3 + X − → CH 2 XCH 3. Similarly, in an H 2 O addition reaction, the pi bond of an alkene acts as a nucleophile and bonds with the proton of an [H 3 ...
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In organic chemistry, a vinyl group (abbr. Vi; [1] IUPAC name: ethenyl group [2]) is a functional group with the formula −CH=CH 2. It is the ethylene (IUPAC name: ethene) molecule ( H 2 C=CH 2 ) with one fewer hydrogen atom.