The decomposition of various N-chloroalkylamines and N-chloroalcoholam
ines was investigated kinetically at pH 4-12 and in strongly alkaline
media, The rate of N-chloramine decomposition increased with increasin
g pH above pH 10, remained virtually constant over the pH range 7-10 a
nd again increased with decreasing pH in the acidic zone, The results
are described by a rate equation involving general base catalysis term
s. Experimental evidence suggests that the decomposition of N-haloamin
es proceeds via an elimination mechanism that yields an imine. This be
ta-elimination process is a non-synchronized concerted mechanism where
cleavage of the N-X bond has progressed to a greater extent than that
of the C-a-H by the time the transition state is reached, which is th
erefore 'E1-like' (ia. with a transition state having a certain nitren
ium character).