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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).
In chemistry, the effective molarity (denoted EM) [1] is defined as the ratio between the first-order rate constant of an intramolecular reaction and the second-order rate constant of the corresponding intermolecular reaction (kinetic effective molarity) [1] [2] or the ratio between the equilibrium constant of an intramolecular reaction and the equilibrium constant of the corresponding ...
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]
A. Kandis Leslie Abdul-Aziz; Linda Abriola; Héctor D. Abruña; Mahdi Abu-Omar; Peter Agre; Joanna Aizenberg; Christopher Alabi; Thomas Albrecht; Millard H. Alexander
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).
A non-bonding orbital, also known as non-bonding molecular orbital (NBMO), is a molecular orbital whose occupation by electrons neither increases nor decreases the bond order between the involved atoms.
The Taft equation is a linear free energy relationship (LFER) used in physical organic chemistry in the study of reaction mechanisms and in the development of quantitative structure–activity relationships for organic compounds. It was developed by Robert W. Taft in 1952 [2] [3] [4] as a modification to the Hammett equation. [5]