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  2. Open Yale Courses - Wikipedia

    en.wikipedia.org/wiki/Open_Yale_Courses

    Open Yale Courses is a project of Yale University to share full video and course materials from its undergraduate courses. Open Yale Courses provides free access to a selection of introductory courses, and uses a Creative Commons Attribution-Noncommercial- Share Alike license.

  3. Outline of organic chemistry - Wikipedia

    en.wikipedia.org/wiki/Outline_of_organic_chemistry

    The following outline is provided as an overview of and topical guide to organic chemistry: Organic chemistry is the scientific study of the structure, properties, composition, reactions, and preparation (by synthesis or by other means) of carbon-based compounds, hydrocarbons, and their derivatives.

  4. Organic chemistry - Wikipedia

    en.wikipedia.org/wiki/Organic_chemistry

    Organic chemistry is a subdiscipline within chemistry involving the scientific study of the structure, properties, and reactions of organic compounds and organic materials, i.e., matter in its various forms that contain carbon atoms. [1]

  5. 1 Course description Toggle the table of contents Wikipedia : United States Education Program/Courses/Advanced Organic Chemistry (Sarjit Kaur)/Course description

  6. Cascade reaction - Wikipedia

    en.wikipedia.org/wiki/Cascade_reaction

    Cascade reactions are often key steps in the efficient total synthesis of complex natural products. The key step in Heathcock's synthesis of dihydroprotodaphniphylline features a highly efficient cascade involving two aldehyde/amine condensations, a Prins-like cyclization, and a 1,5-hydride transfer to afford a pentacyclic structure from an acyclic starting material.

  7. Hapticity - Wikipedia

    en.wikipedia.org/wiki/Hapticity

    This reaction is degenerate and, in the jargon of organic chemistry, it is an example of a sigmatropic rearrangement. [citation needed] A related example is Bis(cyclooctatetraene)iron, in which the η 4 - and η 6-C 8 H 8 rings interconvert. Case 2, typically: complexes containing cyclic polyhapto ligands with maximized hapticity. Such ligands ...

  8. Zaytsev's rule - Wikipedia

    en.wikipedia.org/wiki/Zaytsev's_rule

    In organic chemistry, Zaytsev's rule (or Zaitsev's rule, Saytzeff's rule, Saytzev's rule) is an empirical rule for predicting the favored alkene product(s) in elimination reactions. While at the University of Kazan , Russian chemist Alexander Zaytsev studied a variety of different elimination reactions and observed a general trend in the ...

  9. Physical organic chemistry - Wikipedia

    en.wikipedia.org/wiki/Physical_organic_chemistry

    Physical organic chemistry is the study of the relationship between structure and reactivity of organic molecules.More specifically, physical organic chemistry applies the experimental tools of physical chemistry to the study of the structure of organic molecules and provides a theoretical framework that interprets how structure influences both mechanisms and rates of organic reactions.