The effect of ultrasound on the rates of homogeneous heterolytic react
ions not switched to a free radical pathway can be explained by the pe
rturbation of the molecular organization of or the solvation in the re
acting system. A quantitative analysis of the sonochemical acceleratio
n on the basis of the microreactor concept was carried out. It was fou
nd that (1) the Diels-Alder reaction cannot be accelerated by ultrasou
nd except when SET or free radical processes are promoted, (2) the rec
tified diffusion during cavitation cannot be responsible for the accel
eration of reactions, and (3) the sonochemical acceleration of polar h
omogeneous reactions takes place in the bulk reaction medium. This imp
lies the presence of a 'sound-field' sonochemistry besides the 'hot-sp
ot' sonochemistry. The occurrence of a sonochemical deceleration effec
t can be predicted. (C) 1997 Elsevier Science B.V.