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phenol |
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phenol (fē`nōl), C6H5OH, a colorless, crystalline solid that melts at about 41°C;, boils at 182°C;, and is soluble in ethanol and ether and somewhat soluble in water. An aromatic alcohol alcohol, any of a class of organic compounds with the general formula R-OH, where R represents an alkyl group made up of carbon and hydrogen in various proportions and -OH represents one or more hydroxyl groups . ..... Click the link for more information. , it exhibits weak acidic properties and is corrosive and poisonous. Phenol is sometimes called carbolic acid, especially when in water solution. It reacts with strong bases to form salts called phenolates. Phenol is important in industry in the production of certain artificial resins, e.g., Bakelite Bakelite (bā`kəlīt) [for its inventor, L. H. Baekeland ], synthetic thermosetting resin . ..... Click the link for more information. , and in the synthesis of many drugs, dyes, weed killers, insecticides, and explosives (e.g., picric acid picric acid (pĭk`rĭk) or 2,4,6-trinitrophenol ..... Click the link for more information. ). It is the simplest member of a class of hydroxy benzene derivatives, all of which contain a hydroxyl group hydroxyl group (hīdrŏk`sĭl) ..... Click the link for more information. attached to a benzene benzene (bĕn`zēn, bĕnzēn`), colorless, flammable, toxic liquid with a pleasant aromatic odor. It boils at 80. ..... Click the link for more information. ring; these compounds may be thought of as derivatives of phenol and generically are called phenols. phenolAny of a class of organic compounds with a hydroxyl group (−OH; see functional group) attached to a carbon atom in a ring of an aromatic compound. The simplest one, carbolic acid (C6H5OH), is also called phenol; its most important reaction is with formaldehyde, with which it forms widely used polymers called phenol-formaldehyde (phenolic) resins. Phenols are similar to alcohols but form stronger hydrogen bonds (see bonding), so they dissolve more readily in water and boil at higher temperatures. They may be colourless liquids or white solids; many have a sharp, spicy odour. Some are found in essential oils. Phenols with higher molecular weights and phenol derivatives have supplanted phenol itself as industrial antiseptics (germicidal cleaners). See also Leo Baekeland. phenol 1. a white crystalline soluble poisonous acidic derivative of benzene, used as an antiseptic and disinfectant and in the manufacture of resins, nylon, dyes, explosives, and pharmaceuticals; hydroxybenzene. Formula: C6H5OH 2. Chem any of a class of weakly acidic organic compounds whose molecules contain one or more hydroxyl groups bound directly to a carbon atom in an aromatic ring phenol [′fē‚nȯl] (organic chemistry) C6H5OH White, poisonous, corrosive crystals with sharp, burning taste; melts at 43°C, boils at 182°C; soluble in alcohol, water, ether, carbon disulfide, and other solvents; used to make resins and weed killers, and as a solvent and chemical intermediate. Also known as carbolic acid; phenylic acid. A chemical compound based on the substitution product of phenol, for example, ethylphenol (C2H4C4H5OH), the ethyl substitute of phenol. How to thank TFD for its existence? Tell a friend about us, add a link to this page, add the site to iGoogle, or visit webmaster's page for free fun content. |
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