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Eric V. Anslyn (born June 9, 1960, Santa Monica, California) is an American chemist , University Distinguished Teaching Professor, and Welch Regents Chair in Chemistry at the University of Texas at Austin. [1] He previously held the Norman Hackerman Professorship [citation needed]. Anslyn is co-author of Modern Physical Organic Chemistry, an ...
In 2005 he published a textbook entitled Modern Physical Organic Chemistry with co-author Eric V. Anslyn. Dougherty is the recipient of multiple teaching awards including the Richard Badger Teaching Award (1992), the ASCIT Excellence in Teaching Award (1987 and 2000), and the Richard P. Feynman Prize for Excellence in Teaching (2010).
A. Kandis Leslie Abdul-Aziz; Linda Abriola; Héctor D. Abruña; Mahdi Abu-Omar; Peter Agre; Joanna Aizenberg; Christopher Alabi; Thomas Albrecht; Millard H. Alexander
Hargrove conducted her graduate work with Professors Eric V. Anslyn and Jonathan L. Sessler at the University of Texas, Austin, and earned her Ph.D. in 2010 for her thesis, Combining recognition motifs for improved sensing and biological activity of oligosaccharides and phosphorylated molecules. [5]
Benson group-increment theory (BGIT), group-increment theory, or Benson group additivity uses the experimentally calculated heat of formation for individual groups of atoms to calculate the entire heat of formation for a molecule under investigation.
Example cheletropic reactions: Case 1: the single atom is the carbonyl carbon (C=O) that ends up in carbon monoxide (C≡O). Case 2: the single atom is the nitrogen atom in the diazenyl group (N=N), which ends up as dinitrogen (N≡N).
At standard ambient temperature and pressure, trifluoroperacetic acid is a colourless liquid with a boiling point of 162 °C. [8] It is soluble in acetonitrile, dichloromethane, diethyl ether, and sulfolane, and readily reacts with water. [5]
Allylic strain in an olefin. Allylic strain (also known as A 1,3 strain, 1,3-allylic strain, or A-strain) in organic chemistry is a type of strain energy resulting from the interaction between a substituent on one end of an olefin (a synonym for an alkene) with an allylic substituent on the other end. [1]