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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. Alcohol (chemistry) - Wikipedia

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

    When necessary, the position of the hydroxyl group is indicated by a number between the alkane name and the -ol: propan-1-ol for CH 3 CH 2 CH 2 OH, propan-2-ol for CH 3 CH(OH)CH 3. If a higher priority group is present (such as an aldehyde , ketone , or carboxylic acid ), then the prefix hydroxy- is used, [ 19 ] e.g., as in 1-hydroxy-2 ...

  4. List of carboxylic acids - Wikipedia

    en.wikipedia.org/wiki/List_of_carboxylic_acids

    The systematic IUPAC name is not always the preferred IUPAC name, for example, lactic acid is a common, and also the preferred, name for what systematic rules call 2-hydroxypropanoic acid. This list is ordered by the number of carbon atoms in a carboxylic acid.

  5. Vinyl alcohol - Wikipedia

    en.wikipedia.org/wiki/Vinyl_alcohol

    Vinyl alcohol, also called ethenol (IUPAC name; not ethanol) or ethylenol, is the simplest enol. With the formula C H 2 CH O H , it is a labile compound that converts to acetaldehyde immediately upon isolation near room temperature. [ 1 ]

  6. Homologous series - Wikipedia

    en.wikipedia.org/wiki/Homologous_series

    [1] [2] This can be the length of a carbon chain, [2] for example in the straight-chained alkanes (paraffins), or it could be the number of monomers in a homopolymer such as amylose. [3] A homologue (also spelled as homolog) is a compound belonging to a homologous series. [1]

  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. 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.

  9. 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.