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Mechanism of Nucleophilic Substitution - SN2

The mechanism of nucleophilic substitutions (SN2) is demonstrated.

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Narrative
In SN2 reactions the nucleophile attacks the alkyl halide from the backside of (side opposite) the leaving group.

Discussion
In SN2 (substitution nucleophilic second order) reactions the nucleophile attacks the alkyl halide from the side opposite the leaving group by a direct displacement leading to inversion of configuration. This reaction is very sensitive to steric hindrance and is fastest for primary halides. With tertiary halides, approach of the nucleophile from the backside is blocked.