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  2. Diethyl ether - Wikipedia

    en.wikipedia.org/wiki/Diethyl_ether

    Diethyl ether, or simply ether, is an organic compound with the chemical formula (CH 3 CH 2) 2 O, sometimes abbreviated as Et 2 O. [ a ] It is a colourless, highly volatile , sweet-smelling ("ethereal odour"), extremely flammable liquid .

  3. 2-Cumaranone - Wikipedia

    en.wikipedia.org/wiki/2-Cumaranone

    The Ozonolysis of 2-allylphenol obtained by the alkylation of phenol with 3-bromopropene to produce phenylallyl ether and subsequently its Claisen rearrangement, gives rise to 2-hydroxyphenylacetic acid, which, through water splitting, yields 2-coumaranone. Despite this method having good yields, its economic and safety considerations make it ...

  4. Diethyl ether (data page) - Wikipedia

    en.wikipedia.org/wiki/Diethyl_ether_(data_page)

    Upload file; Special pages ... Get shortened URL; Download QR code; Print/export Download as PDF; Printable version ... Vapor-liquid Equilibrium for Diethyl Ether ...

  5. Oxamide - Wikipedia

    en.wikipedia.org/wiki/Oxamide

    This white crystalline solid is soluble in ethanol, slightly soluble in water and insoluble in diethyl ether. Oxamide is the diamide derived from oxalic acid , and the hydrate of cyanogen . Preparation

  6. Williamson ether synthesis - Wikipedia

    en.wikipedia.org/wiki/Williamson_ether_synthesis

    The Williamson ether synthesis is an organic reaction, forming an ether from an organohalide and a deprotonated alcohol . This reaction was developed by Alexander Williamson in 1850. [ 2 ] Typically it involves the reaction of an alkoxide ion with a primary alkyl halide via an S N 2 reaction .

  7. Mitsunobu reaction - Wikipedia

    en.wikipedia.org/wiki/Mitsunobu_reaction

    The order of addition of the reagents of the Mitsunobu reaction can be important. Typically, one dissolves the alcohol, the carboxylic acid, and triphenylphosphine in tetrahydrofuran or other suitable solvent (e.g. diethyl ether), cool to 0 °C using an ice-bath, slowly add the DEAD dissolved in THF, then stir at room temperature for several hours.

  8. Acetic oxalic anhydride - Wikipedia

    en.wikipedia.org/wiki/Acetic_oxalic_anhydride

    Acetic oxalic anhydride is an unstable colorless crystalline solid, soluble in diethyl ether, that decomposes at about −3 °C into acetic anhydride (H 3 C-(C=O)-) 2 O, carbon dioxide (CO 2) and carbon monoxide (CO). It is hydrolyzed by water into acetic and oxalic acids. [1]

  9. Transition metal ether complex - Wikipedia

    en.wikipedia.org/wiki/Transition_metal_ether_complex

    In chemistry, a transition metal ether complex is a coordination complex consisting of a transition metal bonded to one or more ether ligand. The inventory of complexes is extensive. [2] Common ether ligands are diethyl ether and tetrahydrofuran. Common chelating ether ligands include the glymes, dimethoxyethane (dme) and diglyme, and the crown ...