The products of the gas-phase reactions of the OH radical with n-butyl methyl ether and 2-isopropoxyethanol in the presence of NO have been investigated at 298 ฯฎ 2 K and 740 Torr total pressure of air by gas chromatography and in situ atmospheric pressure ionization tandem mass spectrometry. The pro
Formation of ring-retaining products from the OH radical-initated reactions of o-, m-, and p-xylene
โ Scribed by Roger Atkinson; Sara M. Aschmann; Janet Arey
- Publisher
- John Wiley and Sons
- Year
- 1991
- Tongue
- English
- Weight
- 1007 KB
- Volume
- 23
- Category
- Article
- ISSN
- 0538-8066
No coin nor oath required. For personal study only.
๐ SIMILAR VOLUMES
## Abstract We have carried out relative rate experiments (__T__ = 294 ยฑ 2 K, atmospheric pressure) to investigate the OHโoxidation of __o__โ, __m__โ, and __p__โethyltoluene and __n__โnonane (__k__~1~, __k__~2~, __k__~3~, and __k__~4~ respectively). The experiments were performed in a 2โm^3^ smog c
Rate constants for the gas-phase reactions of 0 3 with the sesquiterpenes a-cedrene, a-copaene, P-caryophyllene, a-humulene, and longifolene, and with the monoterpenes limonene, terpinolene, a-phellandrene, and a-terpinene, have been measured using a relative rate technique at 296 5 2 K and atmosphe
Rate constants for the gas-phase reactions of the four oxygenated biogenic organic compounds cis-3hexen-1-01, cis-3-hexenylacetate, trans-2-hexenal, and linalool with OH radicals, NO3 radicals, and O3 have been determined at 296 2 2 K and atmospheric pressure of air using relative rate methods. The