Chemoselectivity
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Please Take Over This Page and Apply to be Editor-In-Chief for this topic: There can be one or more than one Editor-In-Chief. You may also apply to be an Associate Editor-In-Chief of one of the subtopics below. Please mail us [1] to indicate your interest in serving either as an Editor-In-Chief of the entire topic or as an Associate Editor-In-Chief for a subtopic. Please be sure to attach your CV and or biographical sketch. Chemical reactions are defined usually in small contexts (only up to a small number of neighbouring atoms), such generalizations are a matter of utility. The preferential outcome of one instance of a generalized reaction over a set of other plausible reactions, is defined as chemoselectivity.
Practicing chemists typically try to predict whether or not an instance of a particular generalized reaction will yield product based on the molecular connectivity alone. Such predictions based on connectivity are generally considered plausible, but the physical outcome of the actual reaction is ultimately dependent on a number of factors that are practically impossible to predict to any useful accuracy (solvent, atomic orbitals etc.).
As such, chemoselectivity can be difficult to predict but observing selective outcomes in cases where many reactions are plausible, is common. Examples include the selective organic reduction of 4-nitro-2-chlorobenzonitrile to the corresponding aniline, 4-amino-2-chlorobenzonitrile and the greater relative chemoselectivity of sodium borohydride reduction vs. lithium aluminium hydride reduction.
References
IUPAC Gold Book definition for chemoselectivity[2].
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