The Reaction of O3 with CCl2CH2

1973 ◽  
Vol 51 (10) ◽  
pp. 1504-1510 ◽  
Author(s):  
Leslie A. Hull ◽  
I. C. Hisatsune ◽  
Julian Heicklen

The gas-phase reaction of O3 with CCl2CH2 at 25 °C was studied by monitoring O3 consumption by ultraviolet absorption and product formation and olefin consumption by infrared absorption. In the absence or presence of excess N2, and for initial olefin-to-O3 ratios, [CCl2CH2]0/[O3]0, in excess of 20 ([O3]0 ~ 1.0 Torr), the rate law is[Formula: see text]with k = 2.4 × 106 M−2 s−1. At lower olefin-to-O3 ratios, the rate is initially more rapid than predicted by the above equation, but follows the equation after the reaction has proceeded for some time. In the presence of excess O2, the rate is markedly reduced, and the rate law becomes[Formula: see text]with k′ = 2.2 M−1 s−1.The products of the reaction are CCl2O, HCOOH, CH2ClCCl(O), CO, O2, HCl, and presumably H2O. In the absence of O2, the CCl2CH2-to-O3 consumption ratio approaches 2, but the CCl2O produced per O3 consumed is between 0.25 and 0.4. With excess O2, the latter ratio becomes unity, but the CCl2CH2-to-O3 consumed approaches 5.The results are interpreted in terms of a chain mechanism with CCl2O2 as the chain carrier. The mechanism developed explains the main features of the reaction.

1971 ◽  
Vol 49 (5) ◽  
pp. 803-806 ◽  
Author(s):  
Nick Demchuk ◽  
H. D. Gesser

The gas phase reaction of hydrogen atoms with carbon suboxide was studied over the temperature range of−96 to 235 °C and was found to proceed via a chain reaction. The products found were CH4, CO, CH2CO, C2H6, (CHO)2, and polymer. A mechanism is proposed and the chain reaction is explained by the intermediate formation of ketene and the formyl radical.


2004 ◽  
Vol 218 (4) ◽  
pp. 391-404 ◽  
Author(s):  
Torsten Berndt ◽  
Olaf Böge

AbstractThe gas-phase reaction of O(3P) atoms with benzene was investigated in a flow system in the pressure range of 50–100mbar and a temperature of 295 ± 2K with a focus on the product formation. O2 concentrations in the carrier gas were in the range of (7.7–84) × 1014 molecule cm−3. The primary stable products detected were phenol, benzene oxide/oxepin and a not identified compound with the probable composition C5H6O. The yields of phenol and benzene oxide/oxepin were 0.12 ± 0.02 and 0.26 ± 0.06, respectively, being not affected by the experimental conditions. For benzene oxide/oxepin, a rapid consecutive reaction with O(3P) atoms was observed with a rate coefficient of k(295K) = (1.1 ± 0.1) × 10−10cm3 molecule−1s−1 measured at a pressure of 100mbar. A substance with the formula C6H6O2 (likely oxepin 4,5-epoxide or oxepin 2,3-epoxide), the isomers of muconaldehyde, as well as formic acid, acrolein and trans-butenedial were identified as products of the reaction of O(3P) atoms with benzene oxide/oxepin.


2019 ◽  
Author(s):  
Javad Noroozi ◽  
William Smith

We use molecular dynamics free energy simulations in conjunction with quantum chemical calculations of gas phase reaction free energy to predict alkanolamines pka values. <br>


2021 ◽  
Vol 330 ◽  
pp. 125002
Author(s):  
Yan-Yu Chen ◽  
Yuki Soma ◽  
Masahito Ishikawa ◽  
Masatomo Takahashi ◽  
Yoshihiro Izumi ◽  
...  

ACS Omega ◽  
2021 ◽  
Vol 6 (3) ◽  
pp. 2410-2419
Author(s):  
Junyao Li ◽  
Narcisse T. Tsona ◽  
Shanshan Tang ◽  
Xiuhui Zhang ◽  
Lin Du

1989 ◽  
Vol 24 (10) ◽  
pp. 3679-3685 ◽  
Author(s):  
C. H. Pai ◽  
K. Koumoto ◽  
S. Takeda ◽  
H. Yanagida

2007 ◽  
Vol 44 (6) ◽  
pp. 447-452 ◽  
Author(s):  
Akira Watanabe ◽  
Motoharu Fujii ◽  
Masayoshi Kawahara ◽  
Takehisa Fukui ◽  
Kiyoshi Nogi

2016 ◽  
Vol 27 (5) ◽  
pp. 927-939 ◽  
Author(s):  
Chongming Liu ◽  
Upul Nishshanka ◽  
Athula B. Attygalle

Sign in / Sign up

Export Citation Format

Share Document