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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 10 (1978), S. 1019-1041 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The reactions of ozone with propene and isobutene have been studied in the gas phase at 298°K and 530 Pa (4 torr) using a stopped-flow reactor coupled to a photoionization mass spectrometer. Reactant and product concentrations were followed as a function of reaction time. The major reaction products monitored were CH2O, CH3CHO, CO2, and H2O from the propene reaction, and CH2O, (CH3)2CO, CO2, and H2O from the isobutene reaction. The observations were interpreted on the basis of the Criegee mechanism for ozonolysis in solution: for which we find kA≈kB.In the gas phase the carbene peroxy radical is postulated to isomerize and decompose into molecular and free-radical products.
    Additional Material: 14 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 22 (1990), S. 505-512 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Rate constants have been measured by pulse radiolysis for the reactions of the NO3 radical with five cyclic ethers and a series of alcohols. Rate constants ranged from 3.5 × 104 M×1 s×1 for deuterated methanol to 1.1 × 107 M-1 s-1 for tetrahydrofuran. The rate constants for the reactions of NO3 with the alcohols 1-propanol to 1-heptanol were found to be linearly dependent on the number of CH3 groups with a group reactivity of 6.4 × 105 M-1 s-1.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Rate constants for the gas phase reCedex 2, Franceactions of O(3P) atoms with a series of symmetric aliphatic ethers have been determined using the flash photolysis resonance fluorescence technique over the temperature range 240-400 K. The Arrhenius parameters derived from these data are (in units of cm3 molecule -1 s-1): \documentclass{article}\pagestyle{empty}\begin{document}$$ \begin{array}{rcl} {\rm dimethyl ether,}k &=& (5.39 \pm 1.94) \times 10^{ - 12} {\rm exp[(} - {\rm 1320} \pm 120)/T]; \\ {\rm diethyl ether,}k &=& (1.42 \pm 0.18) \times 10^{ - 11} {\rm exp[(} - {\rm 1070} \pm 40)/T]; \\ {\rm di -}n{\rm - propyle ether,}k &=& (1.41 \pm 0.21) \times 10^{ - 11} {\rm exp[(} - {\rm 960} \pm 50)/T]; \\ {\rm di -}n{\rm - butyl ether,}k &=& (1.37 \pm 0.29) \times 10^{ - 11} {\rm exp[(} - {\rm 880} \pm 70)/T]; \\ {\rm di -}n{\rm - pentyl ether,}k &=& (1.26 \pm 0.84) \times 10^{ - 11} {\rm exp[(} - {\rm 780} \pm 200)/T]; \\ \end{array} $$\end{document}The error limits are two standard deviations derived from the least-squares fit. Rate constants for several other ethers were determined only at 298 K. The values obtained were (in units of 10-14 cm3 molecule-1 s-1): tetrahydrofuran (37.5 ± 1.1); 1,4-dioxane 1(6.81 ± 0.46); diethoxymethane (40.4 ± 1.8); ethyl -t-butyl ether (37.0 ± 1.3); and methyl-t-amylether (57.3 ± 2.3).
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 25 (1993), S. 199-203 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Rate constants have been measured in aqueous solutions for the reactions of the carbonate radical, CO3·-, with several saturated alcohols and one cyclic ether as a function of temperature. Arrhenius pre-exponential factors ranged from 2×108 to 1×109 l mol-1 s-1 and activation energies ranged from 16 to 29 kJ mol-1. The results suggest that the reactions are not pure hydrogen abstraction, but involve an additional interaction of the radical with the —OH or —O— linkage. © 1993 John Wiley & Sons, Inc.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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