When alkyl halides undergo nucleophilic bimolecular substitution which phenomenon is involved

Alternately, an SN2 mechanism in which the formation of the amide oxygen-ribose carbon bond is concurrent with the displacement of the nicotinamide group and proceeds through a pentavalent transition state.

From: Methods in Enzymology, 2016

Alkyl halides undergoing substitution nucleophilic bimolecular reaction involves

Options

(a) formation of carbocation (b) racemic mixture (c) inversion of configuration

(d) retention of configuration

Correct Answer:

inversion of configuration

Explanation:

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