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Nucleophilic Substitution and Elimination Reactions of Alkyl Halides
SN1 Reaction Rate and Unimolecular Step
Description
SN1 reaction rate depends on the substrate, not the nucleophile. This pattern was identified by Sir Christopher Ingold and Edward D. Hughes while they studied nucleophilic substitution reactions of tertiary alkyl halides. A tertiary alkyl halide can still undergo substitution even when the nucleophile is weak.
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Transcript
Rappelons que la vitesse d’une réaction SN2 dépend de la concentration du nucléophile et du substrat. Alors que l’augmentation de la basicité nucléophile augmente le taux de réactions SN2, l’augmentation de l’entrave stérique du substrat diminue la vitesse de réaction.
Cela explique pourquoi les halogénures tertiaire...
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