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  • Physics Chemistry  (51)
  • Wiley-Blackwell  (51)
  • American Institute of Physics (AIP)
  • Springer Nature
  • 1970-1974  (51)
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Publisher
  • Wiley-Blackwell  (51)
  • American Institute of Physics (AIP)
  • Springer Nature
Years
  • 1970-1974  (51)
Year
  • 1
    ISSN: 0538-8068
    Keywords: Chemistry ; Physics Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The gas-phase dehydrogenation of cyclopentene to cyclopentadiene catalyzed by iodine in the range 178-283°C has been found to obey a rate law consistent with the slow rate-determining step, \documentclass{article}\pagestyle{empty}\begin{document}$ {\rm I} + {\rm c} - {\rm C}_5 {\rm H}_8 \stackrel{4}{\rightarrow}{\rm HI} + {\rm c} - {\rm C}_5 {\rm H}_7 $\end{document}, log [k4/(1 mole-1 sec-1)] = 10.25 ± 0.08 - (12.26 ± 0.18)/θ, where θ = 2.303RT in kcal/mole. Surface effects are not important. This value of E4 leads to a value of DHf2980 = 82.3 ± 1 kcal/mole and ΔHf298 = 38.4 ± 1 kcal/mole. From difference in bond strengths in the alkane and the alkene, the allylic resonance stabilization in the cyclopentenyl radical is 12.6 ± 1.0 kcal/mole, in excellent agreement with the value for the butenyl radical.Arrhenius parameters for the other steps in the mechanism are evaluated. The low value of A4 (compared with A4 for cyclopentane) suggests a “tighter” transition state for H-atom abstraction from alkenes than from alkanes.
    Additional Material: 2 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 2 (1970), S. 1-10 
    ISSN: 0538-8068
    Keywords: Chemistry ; Physics Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Reinvestigation of the gas phase thermal reaction of 1,1,2,2-tetramethylcyclopropane (699-759°K) gave for the unimolecular disappearance of reactant, k(TMC) = 1015.27-63.93/θ sec-1, in good agreement with the original results of Frey and Marshall. However, evidence for a high activation energy (E = 79 ± 5 kcal/mole), competitive unimolecular decomposition to 2,3-dimethyl-1 and -2-butenes was also obtained. It is proposed that the serious discrepancy noted [1] between the experimentally observed Arrhenius parameters for the overall reaction kinetics, and those predicted by transition state calculations assuming a biradical mechanism for the isomerization reactions (previously believed to be the only primary reaction mode) can be explained in terms of the increasing importance of the decomposition reactions at higher reaction temperatures.
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 2 (1970), S. 65-68 
    ISSN: 0538-8068
    Keywords: Chemistry ; Physics Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 2 (1970), S. 23-36 
    ISSN: 0538-8068
    Keywords: Chemistry ; Physics Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Dilute mixtures of 4-methyl-l-pentyne have been pyrolyzed in a single-pulse shock tube. The decomposition process involves bond breaking: \documentclass{article}\pagestyle{empty}\begin{document}$$ {\rm HC} \equiv {\rm C} - {\rm CH}_2 ({\rm i - C}_{\rm 3} {\rm H}_{\rm 7} )\stackrel{k_B}{\longrightarrow}{\rm HC} \equiv {\rm C} - {\rm CH}_2 \cdot ({\rm propynyl}) + {\rm i - C}_{\rm 3} {\rm H}_{\rm 7} \cdot $$\end{document} as well as a molecular reaction: \documentclass{article}\pagestyle{empty}\begin{document}$$ {\rm HC}\equiv {\rm C} - {\rm CH}_{\rm 2} ({\rm \rm i - C}_{\rm 3} {\rm H}_{\rm 7} )\stackrel{k_M}{\rightarrow}{\rm C}_{\rm 3} {\rm H}_4 ({\rm allene}) + {\rm C}_3 {\rm H}_6 . $$\end{document} The rate parameters are: \documentclass{article}\pagestyle{empty}\begin{document}$$k_{\bf B} = 10^{15.56} \exp {\rm (} - 34,940/T){\rm (sec}^{ - {\rm 1}}) $$ $$\begin{array}{*{20}c} k_{\rm M} = 10^{13.1} \exp {\rm (} - {\rm 29,670/}T){\rm (sec}^{ - {\rm 1}})&{\rm 1100}^ \circ {\rm K, 1}{\rm .5} - 5{\rm atm}\end{array}$$\end{document} The heat of formation of propynyl radical is thus ΔHf300 = 338 kJ mol-1 (80.7 kcal mol-1)· This leads to a propynyl resonance energy of 40 kJ mol-1 (9.6 kcal mol-1).
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 2 (1970), S. 185-189 
    ISSN: 0538-8068
    Keywords: Chemistry ; Physics Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: O(1D), produced from the photolysis of N2O at 2139 Å, reacts with N2O in accord with: \documentclass{article}\pagestyle{empty}\begin{document} $$ \begin{array}{*{20}c} {(2)} & {{\rm O}(^1 D) + N_2 {\rm O} \to {\rm N}_2 + {\rm O}_2 } \\ \end{array} $$ \end{document}\documentclass{article}\pagestyle{empty}\begin{document} $$ \begin{array}{*{20}c} {(3)} & { \to 2{\rm NO}} \\ \end{array} $$ \end{document}We have used the method of chemical difference to obtain an accurate measure of k2/k3 = 0.59 ± 0.01. Furthermore, the quantum yield of production of O(3P), either on direct photolysis or on deactivation of O(1D) by N2O, is less than 0.02 and probably zero.
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 2 (1970), S. 175-184 
    ISSN: 0538-8068
    Keywords: Chemistry ; Physics Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A method for constructing potential energy surfaces previously proposed by the author has been extended to hydrogen transfer reactions between halide, oxygen, and carbon atoms. A qualitative relation was found between the repulsive energy and the number of anti-bonding electrons. In general, the calculated kinetic isotope effect is in satisfactory agreement with observed values and the contributions by H-atom tunneling to the rate of reaction is smaller than that obtained from other surfaces.
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 2 (1970), S. 265-280 
    ISSN: 0538-8068
    Keywords: Chemistry ; Physics Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The kinetics of the nitric oxide catalyzed, homogeneous, gas-phase isomerization of 1,trans-3,trans-5-heptatriene have been studied for temperatures ranging between 130°C and 241°C. The very clean reaction involves exclusive geometrical isomerization about the 5,6-π-bond. The observed rate constants for \documentclass{article}\pagestyle{empty}\begin{document}$ {\rm NO} + trans - {\rm 3,}trans{\rm - 5}\stackrel{1}{\rightarrow}trans - 3,cis - 5 + {\rm NO} $\end{document} can be represented (with standard errors) by log k1 = (7.18 ± 0.06) - (16.75 ± 0.12)/θ, where θ = 2.303 RT in kcal/mole. The consecutive-step reaction mechanism involves addition of NO to the double bond (Ka, b = ka/kb), followed by rotation of the 5,6-C—C bond in the adduct radical (kc.)Analysis of the observed activation parameters shows, that kc is rate-controlling and consequently k1 = kcKa, b. Estimates of kc and Ka, b lead to a value of k1 in good agreement with experiment.Comparing our data with those previously obtained for the similar 1,3-pentadiene system results in a value for the extra stabilization energy generated in the 1,3-heptadienyl radical of 18.5 ± 1.7 kcal/mole. This value is discussed in view of comparable data in the literature.
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 2 (1970), S. 299-309 
    ISSN: 0538-8068
    Keywords: Chemistry ; Physics Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Arrhenius parameters have been measured for the abstraction of hydrogen from the C Si, Ge, and Sn tetramethyls: \documentclass{article}\pagestyle{empty}\begin{document}$$ \begin{array}{*{20}c} {k({\rm ml m}^{ - {\rm 1}} {\rm s}^{ - {\rm 1}} )} \hfill & {{\rm for}} \hfill & {{\rm C}({\rm CH}_{\rm 3} )_4 = {{10^{12.0} {\rm e}^{ - 8370} } \mathord{\left/ {\vphantom {{10^{12.0} {\rm e}^{ - 8370} } {RT}}} \right. \kern-\nulldelimiterspace} {RT}}} \hfill \\ {k({\rm ml m}^{ - {\rm 1}} {\rm s}^{ - {\rm 1}} )} \hfill & {{\rm for}} \hfill & {{\rm Si(CH}_{\rm 3} {\rm )}_{\rm 4} = {{10^{11.9} {\rm e}^{ - 7300} } \mathord{\left/ {\vphantom {{10^{11.9} {\rm e}^{ - 7300} } {RT}}} \right. \kern-\nulldelimiterspace} {RT}}} \hfill \\ {k({\rm ml m}^{ - {\rm 1}} {\rm s}^{ - {\rm 1}} )} \hfill & {{\rm for}} \hfill & {{\rm Ge(CH}_{\rm 3} {\rm )}_{\rm 4} = {{10^{11.7} {\rm e}^{ - 7370} } \mathord{\left/ {\vphantom {{10^{11.7} {\rm e}^{ - 7370} } {RT}}} \right. \kern-\nulldelimiterspace} {RT}}} \hfill \\ {k({\rm ml m}^{ - {\rm 1}} {\rm s}^{ - {\rm 1}} )} \hfill & {{\rm for}} \hfill & {{\rm Sn(CH}_{\rm 3} {\rm )}_{\rm 4} = {{10^{11.7} {\rm e}^{ - 7250} } \mathord{\left/ {\vphantom {{10^{11.7} {\rm e}^{ - 7250} } {RT}}} \right. \kern-\nulldelimiterspace} {RT}}} \hfill \\ \end{array} $$\end{document} The rate constants correlate with the proton chemical shift, which is related to a polar effect. In all cases except carbon, a hot-molecule β-fluorine rearrangement-elimination reaction occurs following radical combination: \documentclass{article}\pagestyle{empty}\begin{document} $$ ({\rm CF}_3 {\rm CH}_2 {\rm M}({\rm CH}_3 )_3 )^* \to {\rm CF}_2 {\rm CH}_2 + {\rm FM}({\rm CH}_3 )_3 $$ \end{document} We suggest the occurrence of a radical exchange reaction for the Si, Sn, and Ge systems, \documentclass{article}\pagestyle{empty}\begin{document}$$ {\rm CF}_3 + {\rm M}({\rm CH}_3 )_4 \rightleftharpoons{\rm CF}_3 {\rm M}({\rm CH}_3 )_4 \to {\rm CH}_3 + {\rm CF}_3 {\rm M}({\rm C}{\rm H}_3 )_3 $$\end{document} with kexchange (CF3 + Sn(Me)4) ∼ 107 ml m-1 s-1.
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 2 (1970), S. 311-323 
    ISSN: 0538-8068
    Keywords: Chemistry ; Physics Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A check of the data from comparative rate single-pulse shock tube experiments have been carried out through the use of a new standard reaction, the decyclization reaction of ethylcyclobutane. The rate expressions for cyclohexene and 2,2,3-trimethylbutane have been found to be \documentclass{article}\pagestyle{empty}\begin{document}$$ \begin{array}{l} k({\rm C}_{\rm 6} {\rm H}_{{\rm 10}} \to 1,3 - {\rm C}_4 {\rm H}_6 + {\rm C}_2 {\rm H}_4 ) = 10^{15.3} \exp ( - 33,690/T)\sec ^{ - 1} ,950^ \circ - 1100^ \circ {\rm K,2} - {\rm 6atm} \\ k(t{\rm C}_4 {\rm H}_9 - {\rm iC}_3 {\rm H}_7 \to t{\rm C}_{\rm 4} {\rm H}_{\rm 9} \cdot + {\rm iC}_{\rm 3} {\rm H}_7 \cdot ) = 10^{16.5} {{\exp ( - 36,830} \mathord{\left/ {\vphantom {{\exp ( - 36,830} T}} \right. \kern-\nulldelimiterspace} T})\sec ^{ - 1} ,1000^ \circ - 1100^ \circ {\rm K,2} - {\rm 6atm} \\ \end{array} $$\end{document} in excellent agreement with previously published results. Most of the small discrepancy that does exist is apparently due to the differences between the present and earlier (decomposition of isopropyl bromide) "standard" reaction. For the latter process, the present study yields \documentclass{article}\pagestyle{empty}\begin{document}$$ k({\rm iC}_{\rm 3} {\rm H}_7 {\rm Br} \to {\rm C}_{\rm 3} {\rm H}_6 + {\rm HBr}) \to 10^{13.73} {\rm exp(}{{ - 23,970} \mathord{\left/ {\vphantom {{ - 23,970} {T\sec ^{ - 1} ,800^ \circ - 1000^ \circ {\rm K,2} - {\rm 6}}}} \right. \kern-\nulldelimiterspace} {T\sec ^{ - 1} ,800^ \circ - 1000^ \circ {\rm K,2} - {\rm 6}}}{\rm atm)} $$\end{document} These results confirm the correctness of previously published comparative rate single-pulse shock tube experiments. They demonstrate once again that for the decomposition of paraffin hydrocarbons, calculated preexponential factors are at least an order of magnitude higher than the directly measured number and that the accepted value of the heat of formation of t-butyl radicals ΔHf300(tC4H9·) = 29 kJ (6.8 kcals) is at least 10 kJ too low. Finally, attention is called to recent studies on neopentane decomposition in flow and static systems which are in complete agreement with the present conclusions.
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 2 (1970) 
    ISSN: 0538-8068
    Keywords: Chemistry ; Physics Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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