…comparison to other similar reactions, and experimental procedures. UNDECYL ISOCYANATE F. H. Allen and Alan Bell Org. Synth. 1944, 24, 94 DOI: 10.15227/orgsyn.024.0094 An old but reproducible and tested procedure…
Read moreDescription: Addition of strong base to an alkyl halide results in elimination to form a new C–C π bond. The rest of this page is available to MOC Members only….
Read more…bonding of actual organic compounds. The simplest organic compound is methane, CH4. So let’s bring four hydrogen atoms into the picture and try to apply what we’ve learned to come…
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Read more…to amines. 3. The “Hofmann Degradation” Back in 1851, not many techniques for analyzing complex molecules were available. One method for determining the structure of an unknown compound was to…
Read more…that there is free rotation about sigma bonds, so we say, “s-cis” and “s-trans” to distinguish it from “cis” and “trans” configurations which are locked. As we’ll soon see, in…
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Read moreThese practice questions will test you on recognizing conjugated dienes, comparing the reactivity of dienes in the Diels-Alder reaction, providing the major products of Diels-Alder reactions, understanding how to apply…
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Read more…pyranose versus furanose, and all the other most commonly encountered carbohydrate-related terms in a typical second-semester organic chemistry course. [This reference document from IUPAC was extremely helpful in the preparation…
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