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The thermal decomposition of acetaldehyde, propionaldehyde, n -butyraldehyde and iso-butyraldehyde, as investigated by the static method, is essentially homogeneous, inhibitable by propylene, isobutene and small amounts of nitric oxide, and generally catalyzed at high inhibitor concentrations. The kinetic order of the uninhibited decomposition exhibits little obvious regularity, but that of the maximally inhibited reaction is approximately 1.5 for all three inhibitors. Kates of the uninhibited decomposition do not follow the sequence in the homologous series, and there is no systematic variation in the extent of inhibition from one aldehyde to another. For each aldehyde, the minimum rates for the three inhibitors in general are not identical, nevertheless exhibit a correspondence probably close enough to eliminate chance coincidence. The kinetic and analytical results of the uninhibited decomposition can be approximately described by a Kice-Herzfeld-type mechanism, with the kinetics in each case largely determined by the stability of radicals and their reactions in chain propagation and termination. The question whether the maximally inhibited reaction is a molecular reaction or a chain reaction is surveyed. Although the results cannot be completely accounted for by a molecular reaction alone, a chain mechanism for propylene inhibition involving allyl radicals likewise has only limited success. For nitric-oxide inhibition, it is not certain how far the results are affected by the occurrence of the subsequent catalyzed reaction. No definite conclusion can thus be reached about the nature of the maximally inhibited reaction.

The radiolysis of solid solutions of acrylamide and propionamide yields gaseous products which are mainly H2; CO, CH4, and C2He. The yields of hydrogen can be interpreted on the basis of efficient energy transfer from propionamide to acrylamide or by a protective scavenging of hydrogen atoms by the acrylamide double bonds. At any rate, a protective effect similar to that shown in many liquid mixtures can exist in truly crystalline solids. The yields of the other gaseous products are not explainable by energy transfer or scavenging alone and differences in lattice dimensions are believed to play a significant role.

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