Kinetics and Mechanism of Chlorine-Atom-Initiated Oxidation of Allyl Alcohol, 3-Buten-2-ol, and 2-Methyl-3-buten-2-ol

• Published in: The journal of physical chemistry. A, Molecules, spectroscopy, kinetics, environment, & general theory Vol. 114; no. 12; pp. 4224 - 4231
• Main Authors: Takahashi, Kenshi, Xing, Jia-Hua, Hurley, Michael D, Wallington, Timothy J
• Format: Journal Article
• Language: English
• Published: United States American Chemical Society 01.04.2010
• Subjects: A: Atmospheric, Environmental and Green Chemistry; Acetaldehyde - analogs & derivatives; Acetaldehyde - chemistry; Acetone - chemistry; Butanols - chemistry; Carbon - chemistry; Chlorine - chemistry; Formaldehyde - chemistry; Kinetics; Lasers; Oxidation-Reduction; Pentanols - chemistry; Photolysis; Propanols - chemistry; Spectroscopy, Fourier Transform Infrared
• DOI: 10.1021/jp908104r
• ISSN: 1089-5639

The gas-phase reactions of Cl atoms with allyl alcohol (k 1), 3-buten-2-ol (k 2), and 2-methyl-3-buten-2-ol (k 3) at 296 ± 2 K have been investigated using absolute and relative rate methods in 1−700 Torr of N2 diluent. Absolute rate studies were performed using pulsed laser photolysis/vacuum ultraviolet laser-induced fluorescence spectroscopy techniques. Relative rate studies were performed using smog chamber/Fourier transform infrared spectroscopy techniques. The absolute and relative rate studies gave consistent results. The kinetics of the reactions are dependent on pressure over the range studied. Molar yields for HCl production in 700 Torr of N2 for reactions of chlorine atoms with allyl alcohol, 3-buten-2-ol, and 2-methyl-3-buten-2-ol were measured to be 0.26 ± 0.03, 0.23 ± 0.03, and 0.12 ± 0.02, respectively. The chlorine-atom-initiated oxidation of 2-methyl-3-buten-2-ol in 700 Torr of air gave the following products (molar yields): acetone (47 ± 4%), chloroacetaldehyde (47 ± 5%), and HCHO (7.2 ± 0.6%). The observation of substantial and indistinguishable yields of acetone and chloroacetaldehyde products indicates that a major fraction of the reaction proceeds via addition of chlorine atoms to the terminal carbon atom. The results are discussed with respect to the literature data.