Results obtained from the photolysis of ketene with acetylene strongly support the formation of C,H, radicals in the title reaction. Stationary state studies are interpreted in terms of the reaction C,H: 5 C,H, + H with a rate constant (log8 s '1 which is compared to RRKM predictions. In pulsed lase
Are HO radicals produced in the reaction of O(3P) with 1-C4H8?
β Scribed by Menachem Luria; R. Simonaitis; Julian Heicklen
- Publisher
- John Wiley and Sons
- Year
- 1973
- Tongue
- English
- Weight
- 160 KB
- Volume
- 5
- Category
- Article
- ISSN
- 0538-8066
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β¦ Synopsis
The reaction of O p P ) with 1-C4Hs was examined in the presence of CO which scavenges HC) radicals to produce CO,. From the CO, quantum yield, an upper limit to the efficiency of HO production in the reaction of O(3P) with I-CdHs was found to be 0.02 at boi h 298" and 473OK.
Since the classic work of Cvetanovid [l], it has been accepted that O ( 3 P ) reacts with olefins exclusively by addition to the double bond. Recently however, Huie et al. have examined the reaction over the temperature range 190-298"K, which extended their previous work 131 done over the temperature range 259493Β°K. When the two sets of data were combined, a nonlinear Arrhenius plot was obtained. Huie et al.
[2] interpreted this nonlinearity to two processes, addition to the double bond and abstraction of an H atom by the O ( 3 P ) atom.
π SIMILAR VOLUMES
## Abstract Pulse radiolysis techniques were used to measure the gas phase UV absorption spectra of the title peroxy radicals over the range 215β340 nm. By scaling to Ο(CH~3~O~2~)~240 nm~ = (4.24 Β± 0.27) Γ 10^β18^, the following absorption cross sections were determined: Ο(HO~2~)~240 nm~ = 1.29 Β± 0
The reaction of (t-BuGaC12)r with Ar'P(H)Li (Ar' = 2,4,6-t-Bu,C6H2) affords the chloride-bridged dimer [t-BuGa(C1)P(H)Ar'I2 (1). The structure of 1 has been established by X-ray crystallography. Compound 1, C44H7RClZGa2P2, crystallizes in the monoclinic space group P2{ln wit? Z = 2, a = 10.468(1), b
The kinetics of the gas-phase reactions of the OH radical with (C,H,O),PO and (CH30)2P(S)C1 and of the reactions of NO, radicals and O3 with (CH,O),P(S)Cl have been studied at room temperature. Using a relative rate technique, the rate constants determined for the reactions of the OH radical with (C