Chemistry Reference
In-Depth Information
Following initial solvolysis of the tosylate, addition of acetic acid to the carbocation
generates an S
N
1 product. Please note that there is no preservation of the stereo-
chemical configuration in this reaction.
E1 elimination applied to the carbocation formed during solvolysis liberates an
olefin.
Please note: Since the carbocation formed during solvolysis is both tertiary and
allylic, it is very stable and migration reactions are not likely to occur.
S
N
2 displacement of the iodide generates an allylic amine.
