Rate constants have been measured in aqueous solutions for the reactions of the carbonate radical, COs'-, with several saturated alcohols and one cyclic ether as a function of temperature. Arrhenius pre-exponential factors ranged from 2 X lo8 to 1 X lo9 e mol-' s-l and activation energies ranged fr
Rate constants for hydrogen abstraction reactions of the sulfate radical, SO4−. Alkanes and ethers
✍ Scribed by Robert E. Huie; Carol L. Clifton
- Publisher
- John Wiley and Sons
- Year
- 1989
- Tongue
- English
- Weight
- 451 KB
- Volume
- 21
- Category
- Article
- ISSN
- 0538-8066
No coin nor oath required. For personal study only.
✦ Synopsis
Rate constants have been determined for the reactions of SO4with a series of alkanes and ethers. The SO, radical was produced by the laser-flash photolysis of persulfate, SZO: -.
For methane, only an upper limit of 1 x lo6 M-' s-* could be determined. For ethane, propane, and 2-methylpropane, rate constants of 0.44, 4.0, and 10.5 x lo7 M-' s-l were found. For ethyl and n-propyl ether, rate constants of 1.3 x 10' and 2.2 x 10' M-' s-' were found and for 1,4-dioxane and tetrahydrofuran, rate constants of 7.2 x lo7 and 2.8 x 1 0 ' were obtained. The reaction of SO,with ally1 alcohol was also studied and found to have a rate constant of 1.4 x lo9 M-' s-'.
📜 SIMILAR VOLUMES
Absolute rate constants have been measured for the reactions of trichloromethylperoxyl radicals with cyclohexane, cyclohexene, and hexamethylbenzene. The CClsO, radicals were produced by pulse radiolysis of air-saturated CCl, solutions containing various amounts of the hydrocarbons. The rate constan
Rate constants have been measured by pulse radiolysis for the reactions of the NO, radical with five cyclic ethers and a series of alcohols. Rate constants ranged from 3.5 x lo4 M-' 5 -l for deuterated methanol to 1.1 x lo7 M-' 5-l for tetrahydrofuran. The rate constants for the reactions of NO3 wit
An important step in the initial oxidation of hydrocarbons at low to intermediate temperatures is the abstraction of H by hydroperoxyl radical (HO(2)). In this study, we calculate energy profiles for the sequence: reactant + HO(2) → [complex of reactants] → transition state → [complex of products] →
## Abstract Measurements of rates of oxygen absorption and steady‐state peroxy radical concentrations for the autoxidation of tetralin in the presence of __tert__‐butyl hydroperoxide have shown that the rate constant for reaction of the __tert__‐butylperoxy radical with tetralin at 60°C is approxim