1/17
Looks like no tags are added yet.
Name | Mastery | Learn | Test | Matching | Spaced |
---|
No study sessions yet.
rate = [electrophile]
SN1
rate = [nucleophile][electrophile]
SN2
favored by stronger nucleophile
SN2
favored by weaker nucleophile
SN1
favored by less sterically hindered electrophile (1°)
SN2
favored by more highly substituted substrate (3°)
SN1
favored by polar aprotic solvents
SN2
favored by polar protic solvents
SN1
backside attack
SN2
inversion of stereochemistry
SN2
concerted mechanism
SN2
(bonds breaking and forming at the same time)
generates carbocation
SN1
carbocation rearrangements are possible
SN1
product is a mixture
SN1
if chiral carbocation is formed, product mixture will be diastereomers
SN1
step 1: hydrolysis
step 2: coordination
SN1
1 transition state & 1 elementary step
SN2
2 transition states & 2 elementary steps
SN1