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  2. Cross-coupling reaction - Wikipedia

    en.wikipedia.org/wiki/Cross-coupling_reaction

    The leaving group X in the organic partner is usually a halide, although triflate, tosylate, pivalate esters, and other pseudohalides have been used. [15] Chloride is an ideal group due to the low cost of organochlorine compounds. Frequently, however, C–Cl bonds are too inert, and bromide or iodide leaving groups are required for acceptable ...

  3. List of unsolved problems in chemistry - Wikipedia

    en.wikipedia.org/wiki/List_of_unsolved_problems...

    Please help improve this article by adding citations to reliable sources. Unsourced material may be challenged and removed. Unsourced material may be challenged and removed. Find sources: "List of unsolved problems in chemistry" – news · newspapers · books · scholar · JSTOR ( December 2014 ) ( Learn how and when to remove this message )

  4. Organic compound - Wikipedia

    en.wikipedia.org/wiki/Organic_compound

    The study of the properties, reactions, and syntheses of organic compounds comprise the discipline known as organic chemistry. For historical reasons, a few classes of carbon-containing compounds (e.g., carbonate salts and cyanide salts), along with a few other exceptions (e.g., carbon dioxide , and even hydrogen cyanide despite the fact it ...

  5. Socratic (Google) - Wikipedia

    en.wikipedia.org/wiki/Socratic_(Google)

    Socratic is an education tech company that offers a mobile app for students. The app uses AI technology to help students with their homework by providing educational resources like videos, definitions, Q&A, links and more.

  6. 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.

  7. 1,6-Methano(10)annulene - Wikipedia

    en.wikipedia.org/wiki/1,6-Methano(10)annulene

    The classical organic synthesis of this compound starts with Birch reduction of naphthalene to isotetralin, which adds dichlorocarbene (prepared in situ from chloroform and potassium tert-butoxide) to form a transannular cyclopropane ring. A second reduction then removes the chloride substituents.