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  2. 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.

  3. File:Binary phase diagram dioxane-water.svg - Wikipedia

    en.wikipedia.org/wiki/File:Binary_phase_diagram...

    Printable version; Page information; ... Binary vapor-liquid diagram for the system 1,4-dioxane/water ... Version 1.2 or any later version published by the Free ...

  4. File:1-4-Dioxane.svg - Wikipedia

    en.wikipedia.org/wiki/File:1-4-Dioxane.svg

    The following other wikis use this file: Usage on ar.wikipedia.org 4،1-ديوكسان; Usage on be.wikipedia.org Дыаксан; Простыя эфіры

  5. 1,3-Dioxane - Wikipedia

    en.wikipedia.org/wiki/1,3-dioxane

    1,3-Dioxane or m-dioxane is an organic compound with the molecular formula (CH 2) 4 O 2. It is a saturated six-membered heterocycle with two oxygen atoms in place of carbon atoms at the 1- and 3- positions. 1,4-Dioxane, which is of greater commercial value, is an isomer. Both dioxanes are colorless liquids. [1]

  6. 1,2-Dioxane - Wikipedia

    en.wikipedia.org/wiki/1,2-dioxane

    Print/export Download as PDF; Printable version; In other projects Wikidata item; ... 1,2-Dioxane or o-dioxane is an organic compound with the molecular formula ...

  7. Dioxane (compounds) - Wikipedia

    en.wikipedia.org/wiki/Dioxane_(compounds)

    Printable version; In other projects Wikidata item; Appearance. move to sidebar hide ... Dioxane may refer to the following chemical compounds: 1,2-dioxane; 1,3-dioxane;

  8. Prins reaction - Wikipedia

    en.wikipedia.org/wiki/Prins_reaction

    in green: capture of the carbocation by additional carbonyl reactant. In this mode the positive charge is dispersed over oxygen and carbon in the resonance structures 8a and 8b. Ring closure leads through intermediate 9 to the dioxane 10. An example is the conversion of styrene to 4-phenyl-m-dioxane. [6]

  9. Newman projection - Wikipedia

    en.wikipedia.org/wiki/Newman_projection

    Butane molecule represented on a staggered and eclipsed Newman projection down a carbon-carbon bond Butane molecule and all of its possible Newman conformations represented on a relative energy diagram. The diagram takes staggered and eclipsed conformations, as well as gauche and anti interactions into account.