Bordwell pKa Table - Organic Chemistry Data
Oct 27, 2017 · This page by Professor Hans Reich (UW-Madison) provides a collection of common structural motifs in Organic Chemistry and their corresponding pKa values.
4-Amino-1-methoxypyridinium perchlorate >11 67. 2-Aminopyridine 1-oxide 2.67 67. 2-Dimethylaminopyridine 1-oxide. 2.27 67. 8.3 Acetophenone oxime 11.48 Acetoxime 11.42 Isonitrosoacetone (INA) 8.3 Salicyclaldoxime (SA) 9.2 1,2,3-Cyclohexanetrionetrioxime 8.0.
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Equilibrium pKa Table (DMSO Solvent and Reference) Hydrocarbons 20.117 21.822 22.522 17.317 Ph 18.019 26.122 Fluorenes X X = H 22.61 Me 22.31 Ph 17.91 tBu 24.421 SiMe3 21.5 26 SiPh3 18.6 26 = Fl-X
NMR Spectroscopy - Organic Chemistry Data
Feb 14, 2020 · This set of pages originates from Professor Hans Reich (UW-Madison) "Structure Determination Using Spectroscopic Methods" course (Chem 605). It describes Nuclear Magnetic Resonance (NMR) in details relevant to Organic Chemistry.
Nomenclature in Organic Chemistry
4 days ago · A very general and useful rule: if the last part of your name is an actual compound then you are using substituent nomenclature (e.g., benzene, methane, butane, biphenyl, stannane, phosphine are compounds). Your name will be be one word.
Pericyclic Reactions - Organic Chemistry Data
This set of pages originates from Professor Hans Reich (UW-Madison) "Advanced Organic Chemistry" course (Chem 547). It describes chemistry of pericyclic reactions, including mechanisms and examples.
A-8 of chiral lithium amides” Arvidsson, P. I.; Hilmersson, G.; Ahlberg, P. J. Am. Chem. Soc. 1999, 121, 1883-1887. (j) “Composition of the activated complex in ...
Reduction and Oxidation - Organic Chemistry Data
Oct 13, 2024 · This set of pages originates from Professor Hans Reich (UW-Madison) "Advanced Organic Chemistry" course (Chem 547). It describes common reduction and oxidation in Organic Chemistry including typical reducing and oxidizing reagents, their usages, references, and examples in Total Synthesis.
Carbonyl Chemistry - Organic Chemistry Data
This set of pages originates from Professor Hans Reich (UW-Madison) "Advanced Organic Chemistry" course (Chem 547). It describes chemistry of carbonyl compounds, including but not limited to these topics: enolates as nucleophiles; enolate equivalents with higher and lower reactivity; carbonyl groups as electrophiles; and controlling reactivity, regioselectivity, and …