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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 11 (1979), S. 1271-1278 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Experimental evidence is presented for a unimolecular gas-phase Wagner-Meerwein shift in neopentyl chloride pyrolysis. In the decomposition of α,α-neopentyl chloride-d2 at 445°C, maximally inhibited by cyclohexene, the initial products were isotopically pure 2-methyl-1-butene-d2 and 2-methyl-2-butene-d1. Rearrangement, accompanied by loss of either α- or γ-hydrogen in the formation of hydrogen chloride, is consistent with an incipient ion-pair type of transition state. The cyclohexene maximally inhibited pyrolysis of neopentyl chloride was also examined over the temperature range 424-478°C and Arrhenius parameters of E, 258.7 kJ/mole and logA/sec-1, 13.78, were determined.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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