A relationship has been derived between the activation energies E(a) o
f low-temperature non-autocatalyzed thermolysis of nitroparaffins and
their oxygen balances. An analogous relationship has also been found f
or pre-exponents of log A of this thermolysis. The direct relationship
existing between E(a) values and the impact sensitivity of the nitroc
ompounds in a condensed state is confirmed by the first relationship.
From these two relationships, the molecular-structural dependences of
the thermal reactivity of nitroparaffins in both gaseous and liquid st
ates are discussed. For the thermolysis of mononitromethane in the liq
uid state, primary homolytic pseudo-monomolecular fragmentation decomp
osition is hypothesized.