Popular Courses
MCAT
General Course
CHEM 2213
Western University
Organic Chemistry
University Study Guides
Organic Chemistry
General Course
DAT
General Course
CHEM 233
University of British Columbia
CHEM 261
University of Alberta
Organic Chemistry
University Study Guides
CHEM 351
University of Calgary
CHEM 123
University of British Columbia
CHEM 281
Queen's University
CHM 1321
University of Ottawa
CHM136H1
University of Toronto
CHEM 212
McGill University
CHEM 231
University of Victoria
CHEM 2223
Western University
CHM 2120
University of Ottawa
CHEM 353
University of Calgary
CHY 142
Toronto Metropolitan University
CHEM 2401
Dalhousie University

0:00 / 0:00
Molecularity and Rate
The SN2 reaction is bimolecular which means two species are present in the rate equation. Changing the concentration of either species changes the rate!
Wize Concept
SN2 Reactions: Substitution Nucleophilic Bimolecular (2)
Rate = k[substrate][nucleophile]

0:00 / 0:00
Structural Requirements
SN2 reactions occur between a strong nucleophile (NaSEt) and an electrophile with little steric hinderance (Me-I). It is a direct substitution of the leaving group with the nucleophile, in a single step.
Wize Concept
A strong nucleophile is usually negatively charged - watch for sodium (Na) and potassium (K).

0:00 / 0:00
SN2 Mechanism
The SN2 reaction happens in a single step via a crowded transition state.

Wize Concept
Recall: a transition state is something that is formed en route but cannot be spectroscopically observed!
Wize Concept
If you make a chiral product in the SN2 reaction, you will get a single product with inversion of configuration.
Rank the reactivity of the following substrates in the SN2 reaction.
