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8.3: The Mechanisms of Elimination

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    So far in this chapter, we have seen several examples of carbanion-intermediate (E1cb) beta-elimination reactions, in which the first step was proton abstraction at a carbon positioned ato an electron-withdrawing carbonyl or imine. Elimination reactions are also possible at positions that are isolated from carbonyls or any other electron-withdrawing groups. This type of elimination can be described by two model mechanisms: it can occur in a single concerted step (proton abstraction at Cα occurring at the same time as Cβ-X bond cleavage), or in two steps (Cβ-X bond cleavage occurring first to form a carbocation intermediate, which is then 'quenched' by proton abstraction at the alpha-carbon).


    These mechanisms, termed E2 and E1, respectively, are important in laboratory organic chemistry, but are less common in biological chemistry. As explained below, which mechanism actually occurs in a laboratory reaction will depend on the identity of the R groups (ie., whether the alkyl halide is primary, secondary, tertiary, etc.) as well as on the characteristics of the base.

    Organic Chemistry With a Biological Emphasis by Tim Soderberg (University of Minnesota, Morris)

    • Layne A. Morsch (University of Illinois Springfield)

    This page titled 8.3: The Mechanisms of Elimination is shared under a not declared license and was authored, remixed, and/or curated by Layne Morsch.

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