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Addition–elimination reaction

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This is an old revision of this page, as edited by DMacks (talk | contribs) at 13:51, 6 September 2019 (overhaul (NB is was not really correct to call the amine+Schiff "alkylimino-de-oxo-bisubstitution")). The present address (URL) is a permanent link to this revision, which may differ significantly from the current revision.

In chemistry, an addition-elimination reaction is a two-stage reaction process of an addition reaction followed by an elimination reaction. This gives an overall effect of substition, and is the mechanism of the common nucleophilic acyl substitution often seen with esters, amides, and related structures.[1]

Another common type of addition–eliminiation is the reversible reaction of amines with carbonyls to form imines in the alkylimino-de-oxo-bisubstitution reaction, and the analogous reaction of interconversion imines with alternate amine reactants.

The hydrolysis of nitriles to carboxylic acids is also a form of addition-elimination.

References

  1. ^ Reaction-Map of Organic Chemistry Murov, Steven. J. Chem. Educ. 2007, 84, 1224 Abstract