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  2. Diol - Wikipedia

    en.wikipedia.org/wiki/Diol

    Examples include ethane-1,2-diol or ethylene glycol HO−(CH 2) 2 −OH, a common ingredient of antifreeze products. Another example is propane-1,2-diol, or alpha propylene glycol, HO−CH 2 −CH(OH)−CH 3, used in the food and medicine industry, as well as a relatively non-poisonous antifreeze product.

  3. 1,3-Butanediol - Wikipedia

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

    1,3-Butanediol is an organic compound with the formula CH 3 CH(OH)CH 2 CH 2 OH. With two alcohol functional groups, the molecule is classified as a diol. The compound is also chiral, but most studies do not distinguish the enantiomers. The compound is a colorless, bittersweet, water-soluble liquid. It is one of four common structural isomers of ...

  4. 1,3-Propanediol - Wikipedia

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

    1,3-Propanediol is the organic compound with the formula CH 2 (CH 2 OH) 2. This 3-carbon diol is a colorless viscous liquid that is miscible with water. Products

  5. Resorcinol - Wikipedia

    en.wikipedia.org/wiki/Resorcinol

    Benzene-1,3-diol is the name recommended by the International Union of Pure and Applied Chemistry (IUPAC) in its 1993 Recommendations for the Nomenclature of Organic Chemistry. [29] Resorcinol is so named because of its derivation from ammoniated resin gum, and for its relation to the chemical orcinol. [30]

  6. Acetonide - Wikipedia

    en.wikipedia.org/wiki/Acetonide

    General structure of a 1,2-acetonide. The diol is shown in blue, the acetone part in red. In organic chemistry, an acetonide is the functional group composed of the cyclic ketal of a diol with acetone. The more systematic name for this structure is an isopropylidene ketal. Acetonide is a common protecting group for 1,2- and 1,3-diols. [1]

  7. Butanediol - Wikipedia

    en.wikipedia.org/wiki/Butanediol

    2-methylpropane-1,2-diol; 2-methylpropane-1,3-diol; and one unstable geminal diol: 2-methylpropane-1,1-diol (not a glycol), hydrate of 2-methylpropanal (isobutyraldehyde) These three methylpropanediols are structural isomers of butanediols. They are not chiral.

  8. No. 3 Iowa State posts wire-to-wire win vs. No. 25 Baylor - AOL

    www.aol.com/no-3-iowa-state-posts-213240457.html

    Iowa State never trailed, shot 49 percent (24 of 49) from the field and 47.6 percent (10 of 21) from 3-point range. Baylor shot 29.7 percent (19 of 64) overall and 24.1 percent (7 of 29) from ...

  9. Dihydroxybenzenes - Wikipedia

    en.wikipedia.org/wiki/Dihydroxybenzenes

    In organic chemistry, dihydroxybenzenes ... benzene-1,2-diol benzene-1,3-diol benzene-1,4-diol ... All three isomers have the chemical formula C 6 H 6 O 2.