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  2. Diethyl ether (data page) - Wikipedia

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

    Download as PDF; Printable version; In other projects ... Table data obtained from CRC Handbook of Chemistry ... Vapor-liquid Equilibrium for Diethyl Ether/Methanol ...

  3. List of boiling and freezing information of solvents - Wikipedia

    en.wikipedia.org/wiki/List_of_boiling_and...

    Toggle the table of contents. ... Download as PDF; Printable version; In other projects ... Diethyl ether: 0.713 34.5 2.16 –116.3 –1.79

  4. 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 .

  5. Template:Periodic table (with pictures) - Wikipedia

    en.wikipedia.org/wiki/Template:Periodic_table...

    Toggle the table of contents. Template: ... Download as PDF; Printable version; ... element has not been isolated in macroscopic amounts in pure form:

  6. 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 ...

  7. Di-tert-butyl ether - Wikipedia

    en.wikipedia.org/wiki/Di-tert-butyl_ether

    Download as PDF; Printable version; In other projects ... Diethyl ether; Diisopropyl ether; References ... Toggle the table of contents.

  8. 1,4-Dioxane - Wikipedia

    en.wikipedia.org/wiki/1,4-Dioxane

    1,4-Dioxane (/ d aɪ ˈ ɒ k s eɪ n /) is a heterocyclic organic compound, classified as an ether. It is a colorless liquid with a faint sweet odor similar to that of diethyl ether. The compound is often called simply dioxane because the other dioxane isomers (1,2-and 1,3-) are rarely encountered.

  9. 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 .