enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  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. File:1,2-Dioxane.svg - Wikipedia

    en.wikipedia.org/wiki/File:1,2-Dioxane.svg

    Main page; Contents; Current events; Random article; About Wikipedia; Contact us; Pages for logged out editors learn more

  6. 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]

  7. 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 ...

  8. 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;

  9. 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]