Essential Concepts in Organic Chemistry: Reactions and Mechanisms
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Core Concepts in Organic Chemistry
Nucleophilic Substitution Reactions
SN1 Reaction: Unimolecular Substitution
SN1 stands for Substitution Nucleophilic Unimolecular reaction. It proceeds in two steps:
- Slow Step: Dissociation of the substrate to form a carbocation intermediate.
- Fast Step: The carbocation combines with the attacking nucleophile.
Characteristics of SN1 reactions:
- More stable carbocation leads to a faster reaction.
- Favored by polar solvents.
- Mostly given by tertiary alkyl halides.
- Occurs with racemization.
- Follows 1st-order kinetics: Rate = k[R-X].
SN2 Reaction: Bimolecular Substitution
SN2 stands for Substitution Nucleophilic Bimolecular reaction. It proceeds in a single step, which is the rate-determining step.
Characteristics of SN2 reactions:... Continue reading "Essential Concepts in Organic Chemistry: Reactions and Mechanisms" »