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Substitution reactions of some aromatic fluoro compounds /Ho, Ka-cheuk. January 1965 (has links)
Thesis (M. Sc.)--University of Hong Kong, 1966. / Typewritten.
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Effects of substituents containing sulphur and phosphorus atom on aromatic nucleophilic substitution reactions /Wan, Kai-yan. January 1966 (has links)
Thesis (M. Sc.)--University of Hong Kong, 1966. / Typewritten.
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Conformational characterization of abiotic secondary structure based on aromatic stacking /Zych, Andrew John, January 2001 (has links)
Thesis (Ph. D.)--University of Texas at Austin, 2001. / Vita. Includes bibliographical references (leaves 193-199). Available also in a digital version from Dissertation Abstracts.
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Persistence of aromatic compounds in soils and sediments : a molecular perspective /Keiluweit, Marco. January 1900 (has links)
Thesis (M.S.)--Oregon State University, 2010. / Printout. Includes bibliographical references (leaves 62-77). Also available on the World Wide Web.
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Some substitution reactions in rings containing more than one hetero atom陳天樂, Chan, Tin-lok. January 1963 (has links)
published_or_final_version / Chemistry / Master / Master of Science
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Estimating adsorption equilibria of organic compounds on synthetic resinsGroff, Kimberly A. 05 1900 (has links)
No description available.
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Reaction of hydroxyl radical with aromatic hydrocarbonsBenzinger, Stephen B. 24 July 2012 (has links)
Hydroxyl Radical (HO·) is a highly reactive radical species which is an important member of a class of chemical species known as Reactive Oxygen Species (ROS). Hydroxyl radical typically has an extremely short lifetime under most conditions and its highly reactive nature makes it hard to detect by conventional methods used for study of free radical kinetics. In this study we propose and develop an alternative method for relative reactivities and regioselectivities of hydroxyl radical reactions with aromatic compounds in organic solvents. Hydroxyl radical is generated by the thermolysis of a tert-butyl azohydroperoxide which dissociates to yield hydroxyl and tert-butyl radicals, nitrogen, and acetone. TMIO is used to trap the tert-butyl radical, but is less likely to trap hydroxyl radical, which is free to react with the target arene to yield a hydroxycyclohexadienyl species. These species undergo hydrogen abstraction with TMIO to yield phenols, which may be derivatized with an appropriate silylating agent (in this case BTFSA), and analyzed using gas chromatography with detection by flame ionization (GC-FID) and mass spectrometry (GC-MS). The reactivity and selectivity of reaction of hydroxyl radical with various aromatic compounds is determined at different temperatures to obtain relative reaction rates. In this work, the reactivities and selectivities for HO• reactions with simple arenes, such as toluene and naphthalene are investigated. / Department of Chemistry
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Reactivity studies of arene-cis-diols in cycloadditions and potassium permanganate oxidations : synthesis of the corresponding arene-trans-diols and an approach to the synthesis of (+)-pancratistatin /McKibben, Bryan P. January 1994 (has links)
Thesis (Ph. D.)--Virginia Polytechnic Institute and State University, 1994. / Vita. Abstract. Includes bibliographical references (leaves 157-164). Also available via the Internet.
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Biodegradation of BTEX under electron acceptor and nutrient limiting conditions /Cummings, Lorie January 1900 (has links)
Thesis (M. App. Sc.)--Carleton University, 2002. / Includes bibliographical references (p. 166-174). Also available in electronic format on the Internet.
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Toward the synthesis of polycyclic aromatic compounds as nano-carbon cagesZhang, Ruoxin, January 2008 (has links)
Thesis (M.S.)--West Virginia University, 2008. / Title from document title page. Document formatted into pages; contains vii, 45 p. : ill. Includes abstract. Includes bibliographical references (p. 24-26).
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