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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. Ether cleavage - Wikipedia

    en.wikipedia.org/wiki/Ether_cleavage

    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.

  4. Carbocation - Wikipedia

    en.wikipedia.org/wiki/Carbocation

    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]

  5. Reaction intermediate - Wikipedia

    en.wikipedia.org/wiki/Reaction_intermediate

    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 ...

  6. Vinyl group - Wikipedia

    en.wikipedia.org/wiki/Vinyl_group

    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.

  7. Hammond's postulate - Wikipedia

    en.wikipedia.org/wiki/Hammond's_postulate

    However, the BEP principle cannot justify why the energy is lower. Using Hammond's postulate, the lower energy of the tertiary transition state means that its structure is relatively closer to its reactants R(tertiary)-X than to the carbocation product when compared to the secondary case.

  8. The following article contains mild spoilers from the Season 2 premiere of Unstable, now streaming on Netflix. For a light-hearted workplace comedy, the first season of Netflix’s Unstable left ...

  9. Carbenium ion - Wikipedia

    en.wikipedia.org/wiki/Carbenium_ion

    The tert-butyl cation is a relatively stable carbenium ion. [1]A carbenium ion is a positive ion with the structure RR′R″C +, that is, a chemical species with carbon atom having three covalent bonds, and it bears a +1 formal charge.