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  2. Isomer - Wikipedia

    en.wikipedia.org/wiki/Isomer

    For example, in the cyclic alcohol inositol (a six-fold alcohol of cyclohexane), the six-carbon cyclic backbone largely prevents the hydroxyl and the hydrogen on each carbon from switching places. Therefore, one has different configurational isomers depending on whether each hydroxyl is on "this side" or "the other side" of the ring's mean plane.

  3. 1-Hexanol - Wikipedia

    en.wikipedia.org/wiki/1-Hexanol

    Two additional straight chain isomers of 1-hexanol, 2-hexanol and 3-hexanol, exist, both of which differing by the location of the hydroxyl group. Many isomeric alcohols have the formula C 6 H 13 OH. It is used in the perfume industry.

  4. Alcohol (chemistry) - Wikipedia

    en.wikipedia.org/wiki/Alcohol_(chemistry)

    The red and white balls represent the hydroxyl group (−OH). The three "R"s stand for carbon substituents or hydrogen atoms. [1] In chemistry, an alcohol (from Arabic al-kuḥl ' the kohl '), [2] is a type of organic compound that carries at least one hydroxyl (−OH) functional group bound to a saturated carbon atom.

  5. Structural isomer - Wikipedia

    en.wikipedia.org/wiki/Structural_isomer

    Another example is the pair ethanol H 3 C–CH 2 –OH (an alcohol) and dimethyl ether H 3 C–O–CH 2 H (an ether). In contrast, 1-propanol and 2-propanol are structural isomers, but not functional isomers, since they have the same significant functional group (the hydroxyl –OH) and are both alcohols.

  6. 2-Butanol - Wikipedia

    en.wikipedia.org/wiki/2-Butanol

    Like other butanols, butan-2-ol has low acute toxicity. The LD 50 is 4400 mg/kg (rat, oral). [6]Several explosions have been reported [7] [8] [9] during the conventional distillation of 2-butanol, apparently due to the buildup of peroxides with the boiling point higher than that of pure alcohol (and therefore concentrating in the still pot during distillation).

  7. Dihydroxybenzenes - Wikipedia

    en.wikipedia.org/wiki/Dihydroxybenzenes

    All three isomers have the chemical formula C 6 H 6 O 2. Similar to other phenols, the hydroxyl groups on the aromatic ring of a benzenediol are weakly acidic. Each benzenediol can lose an H + from one of the hydroxyls to form a type of phenolate ion.

  8. Butanol - Wikipedia

    en.wikipedia.org/wiki/Butanol

    Butanol (also called butyl alcohol) is a four-carbon alcohol with a formula of C 4 H 9 O H, which occurs in five isomeric structures (four structural isomers), from a straight-chain primary alcohol to a branched-chain tertiary alcohol; [1] all are a butyl or isobutyl group linked to a hydroxyl group (sometimes represented as BuOH, sec-BuOH, i-BuOH, and t-BuOH).

  9. 2-Heptanol - Wikipedia

    en.wikipedia.org/wiki/2-Heptanol

    2-Heptanol is a chemical compound which is an isomer of heptanol. It is a secondary alcohol with the hydroxyl on the second carbon of the straight seven-carbon chain. The compound is flammable and irritant, and through inhalation, ingestion or though skin it can enter into the body. [3] 2-Heptanol is chiral, so (R)- and (S)-isomers exist.