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  2. Phenols - Wikipedia

    en.wikipedia.org/wiki/Phenols

    In organic chemistry, phenols, sometimes called phenolics, are a class of chemical compounds consisting of one or more hydroxyl groups (−O H) bonded directly to an aromatic hydrocarbon group. [1] The simplest is phenol, C 6 H 5 OH. Phenolic compounds are classified as simple phenols or polyphenols based on the number of phenol units in the ...

  3. Phenol - Wikipedia

    en.wikipedia.org/wiki/Phenol

    Phenol (also known as carbolic acid, phenolic acid, or benzenol) is an aromatic organic compound with the molecular formula C6H5OH. [ 5 ] It is a white crystalline solid that is volatile. The molecule consists of a phenyl group (−C6H5) bonded to a hydroxy group (−OH).

  4. Category:Phenols - Wikipedia

    en.wikipedia.org/wiki/Category:Phenols

    Category:Phenols. Category. : Phenols. Wikimedia Commons has media related to Phenols. Phenols are aromatic compounds with a hydroxyl functional group. The chemistry of the hydroxyl group in this chemical environment is substantially different than those found in alcohols .

  5. Phenolphthalein - Wikipedia

    en.wikipedia.org/wiki/Phenolphthalein

    Phenolphthalein (/ fɛˈnɒl (f) θəliːn / [citation needed]feh-NOL (F)-thə-leen) is a chemical compound with the formula C 20 H 14 O 4 and is often written as " HIn ", " HPh ", " phph " or simply " Ph " in shorthand notation. Phenolphthalein is often used as an indicator in acid–base titrations. For this application, it turns colorless in ...

  6. Hydroquinone - Wikipedia

    en.wikipedia.org/wiki/Hydroquinone

    Hydroquinone, also known as benzene-1,4-diol or quinol, is an aromatic organic compound that is a type of phenol, a derivative of benzene, having the chemical formula C 6 H 4 (OH) 2. It has two hydroxyl groups bonded to a benzene ring in a para position. It is a white granular solid.

  7. Phenol red - Wikipedia

    en.wikipedia.org/wiki/Phenol_red

    Chemical structure and properties. Phenol red exists as a red crystal that is stable in air. Its solubility is 0.77 grams per liter (g/L) in water and 2.9 g/L in ethanol. [1] It is a weak acid with p Ka = 8.00 at 20 °C (68 °F). A solution of phenol red is used as a pH indicator, often in cell culture.

  8. Picric acid - Wikipedia

    en.wikipedia.org/wiki/Picric_acid

    The name "picric" comes from Greek: πικρός (pikros), meaning "bitter", due to its bitter taste. It is one of the most acidic phenols. Like other strongly nitrated organic compounds, picric acid is an explosive, which is its primary use. It has also been used as medicine (antiseptic, burn treatments) and as a dye.

  9. Ether - Wikipedia

    en.wikipedia.org/wiki/Ether

    Ether. The general structure of an ether. R and R' represent most organyl substituents. In organic chemistry, ethers are a class of compounds that contain an ether group —an oxygen atom bonded to two organyl groups (e.g., alkyl or aryl). They have the general formula R−O−R′, where R and R′ represent the organyl groups.