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  2. C3H6O2 - Wikipedia

    en.wikipedia.org/wiki/C3H6O2

    The molecular formula C 3 H 6 O 2 may refer to: Acids and esters ... Text is available under the Creative Commons Attribution-ShareAlike 4.0 License; additional terms ...

  3. 1,2-Dioxolane - Wikipedia

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

    1,2-Dioxolane is a chemical compound with formula C 3 H 6 O 2, consisting of a ring of three carbon atoms and two oxygen atoms in adjacent positions. Its condensed structural formula is [–( CH 2 ) 3 –O–O–] .

  4. List of carboxylic acids - Wikipedia

    en.wikipedia.org/wiki/List_of_carboxylic_acids

    C 4 H 9 C(CH 3) 2 COOH 2,3-dimethylhexanoic acid C 3 H 7 ... Text is available under the Creative Commons Attribution-ShareAlike 4.0 License; additional terms may apply.

  5. Enantiomer - Wikipedia

    en.wikipedia.org/wiki/Enantiomer

    [16]: pg. 3 Even though a chiral molecule lacks reflection (C s) and rotoreflection symmetries (S 2n), it can have other molecular symmetries, and its symmetry is described by one of the chiral point groups: C n, D n, T, O, or I. For example, hydrogen peroxide is chiral and has C 2 (two-fold rotational) symmetry.

  6. Structural isomer - Wikipedia

    en.wikipedia.org/wiki/Structural_isomer

    [4] For example, butanol H 3 C−(CH 2) 3 −OH, methyl propyl ether H 3 C−(CH 2) 2 −O−CH 3, and diethyl ether (H 3 CCH 2 −) 2 O have the same molecular formula C 4 H 10 O but are three distinct structural isomers. The concept applies also to polyatomic ions with the same total charge. A classical example is the cyanate ion O=C=N − ...

  7. Dioxolane - Wikipedia

    en.wikipedia.org/wiki/Dioxolane

    It is related to tetrahydrofuran (THF) by replacement of the methylene group (CH 2) at the 2-position with an oxygen atom. The corresponding saturated 6-membered C 4 O 2 rings are called dioxanes. The isomeric 1,2-dioxolane (wherein the two oxygen centers are adjacent) is a peroxide. 1,3-dioxolane is used as a solvent and as a comonomer in ...

  8. Valence isomer - Wikipedia

    en.wikipedia.org/wiki/Valence_isomer

    Tricyclo[4,2,0,0 2,5]octa-3,7-diene. The dimer of cyclobutadiene occurs as a cis isomer and a trans isomer. Both isomers convert to COT (symmetry forbidden hence stable) with a half-life of 20 minutes at 140 °C [ 10 ]

  9. Methyl acetate - Wikipedia

    en.wikipedia.org/wiki/Methyl_acetate

    Methyl acetate is produced industrially via the carbonylation of methanol as a byproduct of the production of acetic acid. [6] Methyl acetate also arises by esterification of acetic acid with methanol in the presence of strong acids such as sulfuric acid; this production process is famous [according to whom?] because of Eastman Kodak's intensified process using a reactive distillation.