Abstract
The relative rates of abstraction by hydrogen atoms of hydrogen and deuterium atoms from propan-2-ol and [2H7]propan-2-ol have been studied, as a function of temperature, in 6 mol dm–3 H2SO4, using both γ-radiation and photolysis of Fe2+ as the source of H. As the temperature is decreased the expected activation control, reflected in an Arrhenius temperature dependence, gives way to diffusion control. Similar behaviour is shown for the same reactions of deuterium atoms in 6 mol dm–3 D2SO4, and for the competition between propan-2-ol and Fe2+ for hydrogen atoms. In all cases, the low temperature behaviour is inadequately described by the diffusional parameters derived in the preceding paper, and a low temperature diffusion process, with an Arrhenius temperature dependence, is proposed to explain the discrepancies. From the competition studies, absolute rate parameters are obtained for the following reactions: (i) H +[2H7]propan-2-ol (abstraction of α-D)A=(6.3 ± 0.5)× 1010 dm3 mol–1 s–1, E= 20 ± 2.6 kJ mol–1, (ii) H +[2H7] propan-2-ol, (abstraction of hydroxylic H)A=(2.5 ± 0.6)× 1010 dm3 mol–1 s–1, E= 23 ± 3 kJ mol–1, (iii) H + Fe2+, A=(1.4 ± 0.6)× 1010 dm3 mol–1 s–1, E= 14 ± 3 kJ mol–1.
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More From: Journal of the Chemical Society, Faraday Transactions 1: Physical Chemistry in Condensed Phases
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