Wize University Organic Chemistry Textbook > Nucleophilic Substitutions and Elimination Reactions
Stereochemistry in Substitution Reactions
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 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

0:00 / 0:00
Stereochemistry in Substitution Reactions
Stereochemistry only needs to be considered when a chiral product is formed. This is usually a consideration when considering secondary carbon electrophiles.
- the SN2 reaction makes one product with inversion of stereochemistry
- the SN1 reaction makes two (or more) products in a racemic mixture (a 50/50 distribution of enantiomers)