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  2. 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.

  3. Open Yale Courses - Wikipedia

    en.wikipedia.org/wiki/Open_Yale_Courses

    Open Yale Courses provides free access to a selection of introductory courses, and uses a Creative Commons Attribution-Noncommercial-Share Alike license. Open Yale Courses launched in December 2007 with seven courses from various departments. The project now includes 40 courses from a broad range of introductory courses taught at Yale college. [1]

  4. Saturated and unsaturated compounds - Wikipedia

    en.wikipedia.org/wiki/Saturated_and_unsaturated...

    For organic compounds containing heteroatoms (other than C and H), the list of unsaturated groups is long but some common types are: carbonyl , e.g. ketones , aldehydes , esters , carboxylic acids (unsaturated) vs alcohol or ether (saturated)

  5. 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]

  6. Free-radical addition - Wikipedia

    en.wikipedia.org/wiki/Free-radical_addition

    In organic chemistry, free-radical addition is an addition reaction which involves free radicals. These reactions can happen due to the free radicals having an ...

  7. Mannich reaction - Wikipedia

    en.wikipedia.org/wiki/Mannich_reaction

    In organic chemistry, the Mannich reaction is a three-component organic reaction that involves the amino alkylation of an acidic proton next to a carbonyl (C=O) functional group by formaldehyde (H−CHO) and a primary or secondary amine (−NH 2) or ammonia (NH 3). [1] The final product is a β-amino-carbonyl compound also known as a Mannich base.

  8. Beilstein database - Wikipedia

    en.wikipedia.org/wiki/Beilstein_database

    The Beilstein database is a database in the field of organic chemistry, in which compounds are uniquely identified by their Beilstein Registry Number.The database covers the scientific literature from 1771 to the present and contains experimentally validated information on millions of chemical reactions and substances from original scientific publications.

  9. Organocatalysis - Wikipedia

    en.wikipedia.org/wiki/Organocatalysis

    When the organocatalyst is chiral an avenue is opened to asymmetric catalysis; for example, the use of proline in aldol reactions is an example of chirality and green chemistry. [10] Organic chemists David MacMillan and Benjamin List were both awarded the 2021 Nobel Prize in chemistry for their work on asymmetric organocatalysis. [11]

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