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The photooxidation of allyl chloride
Author(s) -
Edney Edward O.,
Shepson Paul B.,
Kleindienst Tadeusz E.,
Corse Eric W.
Publication year - 1986
Publication title -
international journal of chemical kinetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.341
H-Index - 68
eISSN - 1097-4601
pISSN - 0538-8066
DOI - 10.1002/kin.550180509
Subject(s) - chemistry , glyoxal , reaction rate constant , formaldehyde , chloride , acrolein , nitrate , allyl chloride , photochemistry , molecule , kinetics , organic chemistry , catalysis , physics , quantum mechanics
The photooxidation of allyl chloride was studied by irradiation either in 100‐L Teflon bags or in a 22.7‐m 3 Teflon smog chamber in the presence of added NO x . In the absence of added hydrocarbons, the reaction involves a Cl atom chain, which leads to a highly reactive system. A reaction mechanism is presented to account for the following photooxidation products: chloroacetaldehyde, formaldehyde, 1,3‐dichloroacetone, 3‐chloroacrolein, acrolein, glyoxal, chloroperoxyacetyl nitrate, and peroxypropenyl nitrate. The rate constant for OH reaction with allyl chloride at 298 K was measured by a relative rate method under conditions where the Cl atom chain length was small and was found to be k OH = 1.7 × 10 −11 cm 3 molecule −1 s −1 . The rate constant for O 3 reaction with allylchloride at 298 K was found to be k O3 = 1.5 × 10 −18 cm 3 molecule −1 s −1 .

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