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CO20. Conjugate Addition-Elimination in Aromatics

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    CO20. Conjugate Addition & Elimination in Aromatics

    In conjugate addition, a carbonyl group turns a neighbouring alkene into an electrophilic site. An enone, such as the one below, has two electrophilic positions.


    A similar situation happens when pi-acceptors such as nitro groups are attached to aromatic rings.


    The key step in the mechanism is the loss of the halide ion, which allows the aromaticity to be restored.


    Problem CO20.2.

    The location of the halogen and the electron-withdrawing group matters. Explain why the reaction occurs if the groups are in the 1 and 2 positions (ortho to each other) or the 1 and 4 positions (para to each other), but not if they are in the 1 and 3 positions (meta to each other).


    Problem CO20.3.

    Explain why the reaction is faster if additional electron-withdrawing groups are present.


    This page titled CO20. Conjugate Addition-Elimination in Aromatics is shared under a CC BY-NC 3.0 license and was authored, remixed, and/or curated by Chris Schaller.

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