Rate coefficients and products for gas-phase reactions of chlorine atoms with cyclic unsaturated hydrocarbons at 298 K

✍ Scribed by A. Sharma; K. K. Pushpa; S. Dhanya; P. D. Naik; P. N. Bajaj

• Publisher: John Wiley and Sons
• Year: 2010
• Tongue: English
• Weight: 145 KB
• Volume: 42
• Category: Article
• ISSN: 0538-8066
• DOI: 10.1002/kin.20467

✦ Synopsis

Abstract

Rate coefficients for the reaction of Cl atoms with cycloalkenes have been determined using the relative rate method, at 298 K and atmospheric pressure of N~2~. Reference molecule was n‐hexane, and the concentrations of the organics were followed by gas chromatographic analysis. Cl atoms were prepared by photolysis of trichloroacetyl chloride at 254 nm. The relative rates of reactions of Cl atoms with cycloalkenes, with respect to n‐hexane, are measured as 1.12 ± 0.38, 1.31 ± 0.14, and 1.69 ± 0.18 for cyclopentene, cyclohexene, and cycloheptene, respectively. Considering the absolute value of the rate coefficient of the reaction of Cl atom with n‐hexane as 3.03 ± 0.06 × 10^−10^ cm^3^ molecule^−1^ s^−1^, the rate coefficient values for cyclopentene, cyclohexene, and cycloheptene are calculated to be (3.39 ± 1.08) × 10^−10^, (3.97 ± 0.43) × 10^−10^, and (5.12 ± 0.55) × 10^−10^ cm^3^ molecule^−1^ s^−1^, respectively. The experiments for each molecule were repeated six to eight times, and the slopes and the rate coefficients given above are the average values of these measurements, and the quoted error includes 2σ as well as all other uncertainties in the measurement and calculations. The rate coefficient increases linearly with the number of carbon atoms, with an increment per additional CH~2~ group being (8.7 ± 1.6) × 10^−12^ cm^3^ molecule^−1^ s^−1^. Chloroketones and chloroalcohols, along with unsaturated ketones and alcohols, were found to be the major products of Cl‐atom‐initiated oxidation of cycloalkenes in the presence of air. The atmospheric implications of these results are discussed, along with a comparison with the reported structure activity relationships. © 2009 Wiley Periodicals, Inc. Int J Chem Kinet 42: 98–105, 2010