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  2. Samarium (II) iodide - Wikipedia

    en.wikipedia.org/wiki/Samarium(II)_iodide

    Samarium(II) iodide. Samarium(II) iodide is an inorganic compound with the formula SmI 2. When employed as a solution for organic synthesis, it is known as Kagan's reagent. SmI 2 is a green solid and forms a dark blue solution in THF. [1] It is a strong one-electron reducing agent that is used in organic synthesis.

  3. Reductions with samarium(II) iodide - Wikipedia

    en.wikipedia.org/wiki/Reductions_with_samarium...

    Since that time, samarium(II) iodide has been employed in a variety of contexts in organic synthesis for both functional group manipulation and carbon-carbon bond formation. Samarium(II) iodide is a one-electron reductant, and typically effects reduction through a series of electron transfer and proton transfer (from protic solvent) steps.

  4. Group 2 organometallic chemistry - Wikipedia

    en.wikipedia.org/wiki/Group_2_organometallic...

    Group 2 organometallic chemistry refers to the organic derivativess of any group 2 element. It is a subtheme to main group organometallic chemistry . [ 2 ] [ 3 ] By far the most common group 2 organometallic compounds are the magnesium-containing Grignard reagents which are widely used in organic chemistry .

  5. 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.

  6. 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]

  7. 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 ...