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  • Articles  (8)
  • Physical Chemistry  (8)
  • Gas chromatography
  • Wiley-Blackwell  (8)
  • 1975-1979
  • 1970-1974  (8)
  • 1974  (8)
  • 1
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 6 (1974), S. 245-256 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The kinetics of N-phenylphthalamic acid and of N-phenylphthalimide hydrolysis in aqueous solutions of sulfuric acid has been studied. A reaction mechanism is proposed implying that unreactive forms of the reactant appear by protonization of the amide bond at the carbonyl oxygen and by dissociation of the o-carboxyl group (N-phenylphthalamic acid). Attack of the nonprotonized amide bond by the hydroxonium ion is suggested to be the rate-limiting step.
    Additional Material: 6 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 6 (1974), S. 531-543 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The effect of reactant self-heating or cooling upon rate data is considered, and three approaches to the problem of obtaining valid kinetic parameters are described in detail. A comparison of these approaches emphasises the need to assess and allow for thermal effects during the initial planning of kinetic experiments if satisfactory results are to be acquired. An integrated rate expression is given for use with nonisothermal data, and is used to provide correction factors for rate constants which have been derived without allowance for thermal effects.
    Additional Material: 6 Tab.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 6 (1974), S. 887-891 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The decaying absorption of CH3 radicals at 216.4 nm has been followed over more than three half-lives using a photoelectric split-beam kinetic spectrometer. The rate constant for recombination kr was found to be (5.60 ± 0.76) × 10-11 cm3/molecule·s.
    Additional Material: 3 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 6 (1974), S. 899-920 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Singlet methylene was reacted with cyclopentadiene to give chemically activated bicyclo[3.1.0]hex-2-ene (BCH). The rate of isomerization of BCH to 1,4-cyclohexadiene, 1,3-cyclohexadiene, cis-1,3,5-hexatriene, and l-methylcyclopentadiene is compared with calculated rate constants using the RRKM theory and measured or estimated thermal Arrhenius parameters. Subsequent isomerizations of the C6H8 products are also measured and calculated. These include 1,4-cyclohexadiene to benzene and the reversible reactions between 1,3-cyclohexadiene, cis-1,3,5-hexatriene, and trans-1,3,5-hexatriene. The results provide new data for several of these reactions which have not been observed in thermal studies. Agreement between the observed and calculated rates using the strong collision assumption is satisfactory except for the trans-1,3,5-hexatriene to cis-1,3,5-hexatriene reaction.
    Additional Material: 7 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 6 (1974), S. 383-394 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: An inhibitor method for measuring the initiation rate is proposed for the system Fe3+ + H2O2. C(NO2)4 was used as inhibitor. The number of chains terminated by one C(NO2)4 molecule was estimated in specific photochemical experiments and found to be unity. The initiation appeared to involve two processes. The first is proportional to the first power of ferric ion concentration, and the second to the second power. The rate constants and activation energies of these processes are determined. Allowance for the second initiation process permitted qualitative and quantitative description of various reported data on H2O2 decomposition rates over a wide range of Fe3+, H2O2, and H+ concentrations.
    Additional Material: 4 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 6 (1974), S. 777-786 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Chloroethanes react with aqueous caustic to yield either elimination or substitution products. The reaction rates were measured for the dichloroethanes, trichloroethanes, tetrachloroethanes, and pentachloroethane between 283 and 353°K. The constants of HCl eleminations referring to the rate equation \documentclass{article}\pagestyle{empty}\begin{document}$$r = k[{\rm OH}^{\rm - }][{\rm dissolved \,substrate]}$$\end{document} are given by \documentclass{article}\pagestyle{empty}\begin{document}$${\rm 1,2 - C}_{\rm 2} {\rm H}_{\rm 4} {\rm Cl}_{\rm 2} {\rm }\,k = 10^{10.99 \pm 0.03} \exp (- 23,000 \pm 50RT)$$\end{document} \documentclass{article}\pagestyle{empty}\begin{document}$${\rm 1,1,2 - C}_{\rm 2} {\rm H}_{\rm 3} {\rm Cl}_{\rm 3} {\rm}\,k = 10^{13.99 \pm 0.03} \exp (- 22,400 \pm 50/RT)$$\end{document} \documentclass{article}\pagestyle{empty}\begin{document}$${\rm 1,1,1,2 - C}_{\rm 2} {\rm H}_{\rm 2} {\rm Cl}_{\rm 4} {\rm }\,k = 10^{15.45 \pm 0.14} \exp (- 25,800 \pm 210/RT)$$\end{document} \documentclass{article}\pagestyle{empty}\begin{document}$${\rm 1,1,2,2 - C}_{\rm 2} {\rm H}_{\rm 2} {\rm Cl}_{\rm 4} {\rm }\,k = 10^{16.40 \pm 0.05} \exp (- 22,550 \pm 70/RT)$$\end{document} \documentclass{article}\pagestyle{empty}\begin{document}$${\rm C}_{\rm 2} {\rm HCl}_{\rm 5} {\rm }\,k = 10^{12.50 \pm 0.08} \exp (- 15,200 \pm 110/RT)$$\end{document} all rate constants being in 1./mole·s and R in cal/mole· deg.With ethyl chloride, 1,1-dichloroethane, and 1,1,l-trichloroethane, the elimination is not observed and a slow substitution takes place. The influence of chlorine substituents on both sides of the molecule on mechanism and rate parameters is discussed.
    Additional Material: 4 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 6 (1974), S. 359-370 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The four species in the title were decomposed under VLPP conditions at temperatures in the vicinity of 1100°K. Three model transition states were constructed that fit the low-pressure data thus obtained and that also yield (1) E298 = ΔE298; (2) E1100 = ΔE1100; (3) log A1100 = 16.4 per C-C bond broken. The predictions of these models as to values of the high-pressure rate constants for bond scission and the reverse rate constants (radical combination) are compared with existing data.
    Additional Material: 4 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 6 (1974), S. 617-630 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The reactions \documentclass{article}\pagestyle{empty}\begin{document}$$\begin{array}{*{20}c} {(1)} {{\rm O + HNO}_3 \to {\rm products}}\\ {(2)} {{\rm H + HNO}_{\rm 3} \to {\rm products}} \end{array}$$\end{document} have been studied in a discharge-flow system. Kinetic studies were made using resonance fluorescence for the measurement of atom concentrations. Based on the rates of atom loss, the following upper limits were obtained for the rate constants: \documentclass{article}\pagestyle{empty}\begin{document}$$ k_1 \le 3 \times 10^{ - 17} {\rm cm}^{\rm 3} /{\rm molec - sec} $$\end{document} \documentclass{article}\pagestyle{empty}\begin{document}$$ k_1 \le 2 \times 10^{ - 15} {\rm cm}^{\rm 3} /{\rm molec - sec} $$\end{document} Observed reaction in the H—HNO3 system is at least partially due to an autocatalytic chain removal of both reactants. Diagnostic tests have suggested that OH, NO2, and NO3 are the chain carriers.
    Additional Material: 2 Ill.
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