Haloform Reaction
…ACID M. S. Newman and H. L. Holmes Org. Synth. 1937, 17, 65 DOI: 10.15227/orgsyn.017.0065 β,β-DIMETHYLACRYLIC ACID Lee Irvin Smith, W. W. Prichard, and Leo J. Spillane Org. Synth. 1943,…
Read more…ACID M. S. Newman and H. L. Holmes Org. Synth. 1937, 17, 65 DOI: 10.15227/orgsyn.017.0065 β,β-DIMETHYLACRYLIC ACID Lee Irvin Smith, W. W. Prichard, and Leo J. Spillane Org. Synth. 1943,…
Read more…Someday I’ll put together a more comprehensive summary sheet of this stuff – there’s certainly a lot more that could go in. Click for enlarged image, or download the PDF…
Read more…Reactions. IV. The Hydrolysis of Tertiary Enamines in Acidic Medium W. Maas, M. J. Janssen, E. J. Stamhuis, H. Wynberg. Journal of Organic Chemistry, 1967, 32, 1111 DOI: 10.1021/jo01279a056 Detailed…
Read more…SECONDARY AMINES DOUGLAS G. NORTON, VERNON E. HAURY, FRANK C. DAVIS, LLOYD J. MITCHELL, and SEAVER A. BALLARD J. Org. Chem., 1954, 19 (7), 1054-1066 DOI: 10.1021/jo01372a010 An old but…
Read more…what is meant by isopropyl, tert-butyl and more. 2. Isomers and Stereochemistry structural isomers (constitutional isomers) [video] conformational isomers including Newman and Chair Chirality including R/S, D/L, enantiomers, diastereomers, meso…
Read more…order. Instead we look at the ‘m’ in methyl and ‘e’ in ethyl. Since ‘e’ comes before ‘m’ ethyl comes before dimethyl. This also applies ‘tri’, ‘tetra’, etc. The prefix…
Read moreHere’s something I don’t understand. Well, that’s not true – it’s something I understand, but I think is… unwise. Bringing a model kit to an exam and never using it….
Read more…discouraged. HELP PLEASE. Anyone who survived this…..THING….share your wisdom! (I’m….serious……>=( ). Thanks! After scrolling through about 20 different answers (more on that subject in a later post), I hastily scrawled…
Read more…old book. It was “Elements of Organic Chemistry” by Richards, Cram, and Hammond. 1968. I leafed through it. I always *did* like organic chemistry, I thought. “Mind if I borrow…
Read more…fizzing”, said Docherty. 12:10 p.m. “‘Tis Orange!” After warming to room temperature, the reaction had turned orange [color is a parts-per-million phenomenon, so this can often be a misleading indication…
Read more