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Nucleophilic Substitution and Elimination Reactions of Alkyl Halides
SN1 Pathway and Product Chirality
Description
SN1 reactions can change the chirality of a product because the reaction goes through a carbocation intermediate. First, the bond between the electrophilic carbon and the leaving group ionizes. Then the nucleophile attacks the carbocation.
The carbocation formed in an SN1 reaction is sp2 hybridiz...
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Transcript
In nucleophilic substitution reactions, the stereochemical outcome of the product, that is, inversion or retention of configuration, can be studied if substitution occurs in a chiral substrate.
SN2 reactions are stereospecific since the nucleophile directly attacks the substrate from the backside, which invariably results in a...
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