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  • 1
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 16 (1984), S. 1161-1166 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The reaction \documentclass{article}\pagestyle{empty}\begin{document}${\rm Br} + {\rm CH}_3 {\rm CHO}\buildrel1\over\rightarrow{\rm HBr} + {\rm CH}_3 {\rm CO}$\end{document} has been studied by VLPR at 300 K. We find k1 = 2.1 × 1012 cm3/mol s in excellent agreement with independent measurements from photolysis studies. Combining this value with known thermodynamic data gives k-1 = 1 × 1010 cm3/mol s. Observations of mass 42 expected from ketene suggest a rapid secondary reaction: \documentclass{article}\pagestyle{empty}\begin{document}$${\rm Br} + {\rm CH}_3 {\rm CO}\buildrel2\over\rightarrow[{\rm CH}_3 {\rm COBr}]^* \buildrel3\over\rightarrow{\rm HBr} + {\rm CH}_2 {\rm CO}$$\end{document} in which step 2 is shown to be rate limiting under VLPR conditions and k2 is estimated at 1012.6 cm3/mol s from recent theoretical models for radical recombination. It is also shown that 0 ≤ E1 ≤ 1.4 kcal/mol using theoretical models for calculation of A1 and is probably closer to the lower limit. Reaction -1 is negligible under conditions used.
    Zusätzliches Material: 1 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 2
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 16 (1984), S. 995-1008 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The very low pressure reactor (VLPR) technique has been used to measure the bimolecular rate constant of the title reaction at 300 K. The rate constant is given by log k1 (1/mol s) = (11.6 ± 0.4) - (5.9 ± 0.6)/θ the equilibrium constant has also been measured at the same temperature and is given by K1 = (5.6 ± 1) × 10-3 and hence log k-1 (1/mol s) = 9.5 ± 0.1. The results show that the reaction Br + t—C4H9 → HBr + i—C4H8 is unimportant under the present experimental conditions. Assigning the entropy of t-butyl radical to be 74 ± 2 eu which is in the possible range, the value of K1 gives ΔH°f (t-butyl) = 9.1 ± 0.6 kcal/mol-1. This yields for the bond dissociation, DH° (t-butyl-H) = 93.4 ± 0.6 kcal/mol. Both of these values are found to be in good agreement with recent VLPP studies.
    Zusätzliches Material: 2 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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