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phenol

phenol

phenol Sentence Examples

  • In order to obtain the phenol from this distillate, it is treated with caustic soda, which dissolves the phenol and its homologues tegether with a certain quantity of naphthalene and other hydrocarbons.

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  • This layer is separated, and the phenol recovered by a process of fractional distillation.

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  • In order to obtain the phenol from this distillate, it is treated with caustic soda, which dissolves the phenol and its homologues tegether with a certain quantity of naphthalene and other hydrocarbons.

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  • This layer is separated, and the phenol recovered by a process of fractional distillation.

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  • He recommended that yeast should be purified by cultivating it in a solution of sugar containing tartaric acid, or, in wort containing a small quantity of phenol.

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  • It has a characteristic smell, and a biting taste; it is poisonous, and acts as a powerful antiseptic. It dissolves in water, 15 parts of water dissolving about one part of phenol at 16-17° C., but it is miscible in all proportions at about 70° C.; it is volatile in steam, and is readily soluble in alcohol, ether, benzene, carbon bisulphide, chloroform and glacial acetic acid.

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  • When phenol is passed through a red-hot tube a complex decomposition takes place, resulting in the formation of benzene, toluene, naphthalene, &c. (J.

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  • Chromium oxychloride reacts violently on phenol, producing hydroquinone ether, O(C 6 H 4 OH)2; chromic acid gives phenoquinone, and potassium permanganate gives paradiphenol, oxalic acid, and some salicylic acid (R.

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  • The hydrogen of the hydroxyl group in phenol can be replaced by metals, by alkyl groups and by acid radicals.

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  • The metallic derivatives (phenolates, phenates or carbolates) of the alkali metals are obtained by dissolving phenol in a solution of a caustic alkali, in the absence of air.

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  • The alkyl derivatives may be obtained by heating phenol with one molecular proportion of a caustic alkali and of an alkyl iodide.

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  • O CH 3, is prepared either by the above method or by the action of diazomethane on phenol, C6HSOH+CH2N2=N2+C6H5.

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  • O Coch 3, a colourless liquid of boiling point 193° C., may be prepared by heating phenol with acetamide.

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  • When heated with aniline it yields phenol and acetanilide.

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  • O COC 6 H 5, prepared from phenol and benzoyl chloride, crystallizes in monoclinic prisms, which melt at 68-69° C. and boil at 314° C.

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  • Phenol is characterized by the readiness with which it forms substitution products; chlorine and bromine, for example, react readily with phenol, forming orthoand parachlorand -bromphenol, and, by further action, trichlorand tribrom-phenol.

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  • lodphenol is obtained by the action of iodine a.nd iodic acid on phenol dissolved in a dilute solution of caustic potash.

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  • Nitro-phenols are readily obtained by the action of nitric acid on phenol.

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  • Phenol dissolves readily in concentrated sulphuric acid, a mixture of phenol-orthoand -para-sulphonic acids being formed.

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  • A thiophenol, C 6 H 5 SH, is known, and is prepared by the action of phosphorus pentasulphide on phenol, or by distilling a mixture of sodium benzene sulphonate and potassium sulphydrate.

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  • Vortmann (Ber., 1890, 23, p. 2 753) dissolve phenol in caustic alkali, make the solution up to known volume, take an aliquot part, warm it to 60° C., and add decinormal iodine solution until the liquid is of a deep yellow colour.

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  • Industry, 1899, 18, p. 553) adds excess of sodamide to a solution of the phenol in a suitable solvent, absorbs the liberated ammonia in an excess of acid, and titrates the excess of acid.

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  • When fused with caustic potash it yields phenol and salicylic acid.

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  • Xanthene, C13H100, may be synthesized by condensing phenol with ortho-cresol in the presence of aluminium chloride.

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  • In the first thesis, phenol or oxybenzene,C 6 H 5.

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  • These three acids yield on heating phenol, identical with the substance started with, and since in the three oxybenzoic acids the hydroxyl groups must occupy positions other than I, it follows that four hydrogen atoms are equal in value.

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  • Substitution of the Benzene Ring.-As a general rule, homologues and mono-derivatives of benzene react more readily with substituting agents than the parent hydrocarbon; for example, phenol is converted into tribromphenol by the action of bromine water, and into the nitrophenols by dilute nitric acid; similar activity characterizes aniline.

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  • Potassium chlorate and hydrochloric acid oxidize phenol, salicylic acid (o-oxybenzoic acid), and gallic acid ([2.3.4] trioxybenzoic acid) to tri chlorpyroracemic acid (isotrichlorglyceric acid), CC13 C(OH)2 C02H, a substance also obtained from trichloracetonitrile, CC1 3 CO CN, by hydrolysis.

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  • CC13+C02 O?OIi O / O / (4) Cl2HC CO CHCl2+CH302C CCl2C02CH3 (5) Cl2HC CONH2 Cl (z) (2) When phenol is oxidized in acid solution by chlorine, tetrachlorquinone is obtained, a compound also obtainable from hydroquinone.

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  • When thus chlorinated phenol (I) yields trichlor-o-diketo-R-hexene (2), which may be hydrolysed to an acid (3), which, in turn, suffers rearrangement to trichlor-R-pentene-oxycarboxylic acid (4).

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  • 26, water 3.81-2.32; phenol, nitric acid, sulphuric acid, nitroethane, and propionitril, also exhibit association.

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  • Reimer, Ber., 1876, 9, p. 1285); and by the action of sodium on a mixture of phenol and chlorcarbonic ester (T.

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  • Sodium phenolate is heated in a stream of carbon dioxide in an iron retort at a temperature of 180-220° C., when half the phenol distils over and a basic sodium salicylate is left.

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  • Manasse (German patent 73,279) prepared an intimate mixture of phenol and potassium carbonate, which is then heated in a closed vessel with carbon dioxide, best at 130 -160 C. The Chemische Fabrik vorm.

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  • Hofmann and Schotensack decompose a mixture of phenol (3 molecules) and sodium carbonate (4 mols.) with carbonyl chloride at 140-zoo° C. When 90% of the phenol has distilled over, the residue is dissolved and hydrochloric acid added, any phenol remaining is blown over in a current of steam, and the salicylic acid finally precipitated by hydrochloric acid.

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  • It sublimes, but on rapid heating decomposes into carbon dioxide and phenol.

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  • It yields both esters and ethers since it is an acid and also a phenol.

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  • When boiled with aniline it gives methylaniline and phenol.

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  • Phenyl salicylate, C6H4(OH) C 02C6H5, or salol, is obtained by heating salicylic acid, phenol and phosphorus oxychloride to 120-125° C.; by heating salicylic acid to 2 =0° C.; or by heating salicyl metaphosphoric acid and phenol to 140-150° C. (German Patent 85,565).

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  • When heated in air for many hours it decomposes, yielding carbon dioxide, phenol and xanthone.

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  • It is usually prepared by the so-called "Reimer" reaction (Ber., 1876, 9,p. 1268), in which chloroform acts on phenol in the presence of a caustic alkali, C 6 H 5 OH+CHC1 3 +4KHO = 3KCI+3H20+KO�C6H4�CHO, some para-oxybenaldehyde being formed at the same time.

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  • The latter on reduction yields a diamino compound, the disulphonic acid of which on diazotization and coupling with a phenol, &c., gives valuable substantive cotton dyes after the type yielded by Benzidine.

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  • It solidifies in a freezing mixture, on the addition of a crystal of phenol, and then melts at 3 0 -4° C. It boils at 202° 8 C. Its aqueous solution is coloured bluish-violet by ferric chloride.

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  • The secondary amines may be of two types-namely,the purely aromatic amines, and the mixed secondary amines, which contain an aromatic residue and an alkyl group. The purely aromatic amines result upon heating the primary amines with their hydrochlorides, and, in some cases, by heating a phenol with a primary amine and anhydrous zinc chloride.

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  • Picric acid can also be obtained from it by first treating acetylene with sulphuric acid, converting the product into phenol by solution in potash and then treating the phenol with fuming nitric acid.

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  • soc. chim., 18 94 (3) 11, p. 1129) obtained anilino-derivatives of the paraquinones by the action of an aqueous solution of potassium chromate on an acetic acid solution of para-aminodimethylaniline and phenol: C 6 H 5 OH+H 2 N C 6 H 4 N (CH 3) 2 - *O:C 6 H 4 :N C 6 H 4 N(CH 3) 2; these compounds yield the quinone when heated with mineral acids.

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  • They may be prepared by the reduction of nitro compounds in alkaline solution (using zinc dust and alkali, or a solution of an alkaline stannite as a reducing agent); by oxidation of hydrazo compounds; or by the coupling of a diazotized amine and any compound of a phenolic or aminic type, provided that there is a free para position in the amine or phenol.

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  • The oxyazo compounds are prepared by adding a solution of a diazonium salt to a cold slightly alkaline solution of a phenol.

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  • Para-oxyazobenzene (benzene-azo-phenol), C 6 H 5 N: N (1) C6H4 011(4), is prepared by coupling diazotized aniline with phenol in alkaline solution.

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  • The more complete phenomena of mutual solubility are illustrated by the case of phenol and water.

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  • 4 A represents the freezing point of pure water, and AB the freezing point curve showing the depression of the freezing point as phenol is added.

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  • At B is a nonvariant system made up of ice, solid phenol, saturated solution and vapour.

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  • BCD c is the solubility curve of phenol in water.

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  • At C a new o° A C liquid phase appears - the B solution of water in liquid ' r q Ivater 50 Phenol phenol, the solubility of which FIG.

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  • Replacement of -NH 2 by-OH:-The amine is diazotized and the aqueous solution of the diazonium salt is heated, nitrogen being eliminated and a phenol formed.

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  • It may be condensed to a liquid, which boils at about o° C. It is a powerful methylating agent, reacting with water to form methyl alcohol, and converting acetic acid into methylacetate, hydrochloric acid into methyl chloride, hydrocyanic acid into acetonitrile, and phenol into anisol, nitrogen being eliminated in each case.

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  • Pasteur, Ann., 1853, 88, p. 212); by heating tartaric or racemic acid for some time with water to 165° C.; by the oxidation of laevulose; and by the oxidation of phenol or maleic acid with an alkaline solution of potassium permanganate (0.

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  • It may be prepared synthetically by fusing meta-iodophenol, phenol meta-sulphonic acid, and benzene meta-disulphonic acid with potash; by the action of nitrous acid on meta-aminophenol; or by the action of 10% hydrochloric acid on meta-phenylene diamine (J.

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  • (2) Argenti oxidum, incompatible with chlorides, organic substances, phenol, creosote, &c., with which it forms explosive compounds.

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  • Carum copticum, from which it may be extracted by shaking with potassium hydroxide, filtering and precipitating the phenol with hydrochloric acid.

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  • Cyclo-hexanone, C 6 H 10 0, is obtained by the distillation of calcium pimelate, and by the electrolytic reduction of phenol, using an alternating current.

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  • Phenol.

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  • It retains some of the nutrients found in raw cane S Return to Top Salicylates Salicylates are a type of Phenol.

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  • Mix 25 ml phenol with 25 ml chloroform in a 150 ml bottle.

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  • Swinburne became interested in plastics in 1902 when he was introduced to the phenol formaldehyde reaction.

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  • Human Mixtard 30 Pen also contains glycerol, sodium phosphate, protamine sulfate as retarding agent and m-cresol and phenol as added preservative.

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  • micronucleusdata indicate that phenol can produce hypothermia in mice at doses that result in micronuclei formation.

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  • This analog contains the phenol moiety of tyrosine and thus the contacts that drive the chemistry and define the TPL specificity can be identified.

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  • Peripheral nerve block using phenol is a relatively old technique.

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  • Fears were expressed that other cancer causing chemicals including phenol and benzene are also polluting the site.

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  • Paraplegia from injecting phenol into the arteries that supply the spinal cord (prevented by checking the needle position with radio-opaque dye ).

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  • In the case of a phenol, you can react the phenol with sodium hydroxide solution first, producing the more reactive phenoxide ion.

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  • For neurolytic blocks (arterial insufficiency) 3 - 5 ml 6% aqueous phenol is injected.

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  • phenol into the arteries that supply the spinal cord (prevented by checking the needle position with radio-opaque dye ).

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  • phenol formaldehyde reaction.

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  • phenol extraction and ethanol precipitation.

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  • phenol levels uses up more than the usual amounts of the ' free sulfate ' which is held in the gut.

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  • phenol plants at the Fallujah II facility.

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  • phenol red and dissolve.

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  • phenol injections and/or gassing is halted.

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  • Paints The main substances of concern likely to be found in paints are alkyl phenol ethoxylates, chlorinated paraffins and phthalates.

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  • The top layer is a solution of phenol in water, and the bottom one a solution of water in phenol in water, and the bottom one a solution of water in phenol.

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  • Investigations in phenol formaldehyde resins for example elucidate mechanism and provide new flame retardant materials.

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  • Phenol tends to burn in air with an extremely smoky flame - full of carbon particles.

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  • He recommended that yeast should be purified by cultivating it in a solution of sugar containing tartaric acid, or, in wort containing a small quantity of phenol.

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  • Lignified tissues are colored yellow by aniline sulphate or aniline chloride, violet with phloroglucin and hydrochloric acid, and characteristic reactions are also given by mixtures containing phenol, indol, skatol, thailin, sulphate, &c. (see Zimmermanns Microtechnique).

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  • CARBOLIC ACID or Phenol (hydroxy-benzene), C 6 H 5 OH, an acid found in the urine of the herbivorae, and in small quantity in castoreum (F.

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  • Phys., 1888 (6) 14, p. 435); by heating phenol carboxylic acids with baryta; and, in small quantities by the oxidation of benzene with hydrogen peroxide or nascent ozone (A.

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  • It has a characteristic smell, and a biting taste; it is poisonous, and acts as a powerful antiseptic. It dissolves in water, 15 parts of water dissolving about one part of phenol at 16-17° C., but it is miscible in all proportions at about 70° C.; it is volatile in steam, and is readily soluble in alcohol, ether, benzene, carbon bisulphide, chloroform and glacial acetic acid.

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  • When phenol is passed through a red-hot tube a complex decomposition takes place, resulting in the formation of benzene, toluene, naphthalene, &c. (J.

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  • Chromium oxychloride reacts violently on phenol, producing hydroquinone ether, O(C 6 H 4 OH)2; chromic acid gives phenoquinone, and potassium permanganate gives paradiphenol, oxalic acid, and some salicylic acid (R.

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  • The hydrogen of the hydroxyl group in phenol can be replaced by metals, by alkyl groups and by acid radicals.

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  • The metallic derivatives (phenolates, phenates or carbolates) of the alkali metals are obtained by dissolving phenol in a solution of a caustic alkali, in the absence of air.

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  • The alkyl derivatives may be obtained by heating phenol with one molecular proportion of a caustic alkali and of an alkyl iodide.

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  • O CH 3, is prepared either by the above method or by the action of diazomethane on phenol, C6HSOH+CH2N2=N2+C6H5.

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  • The acid esters of phenol are best obtained by the action of acid chlorides or anhydrides on phenol or its sodium or potassium salt, or by digesting phenol with an acid in the presence of phosphorus oxychloride (F.

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  • O Coch 3, a colourless liquid of boiling point 193° C., may be prepared by heating phenol with acetamide.

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  • When heated with aniline it yields phenol and acetanilide.

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  • O COC 6 H 5, prepared from phenol and benzoyl chloride, crystallizes in monoclinic prisms, which melt at 68-69° C. and boil at 314° C.

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  • Phenol is characterized by the readiness with which it forms substitution products; chlorine and bromine, for example, react readily with phenol, forming orthoand parachlorand -bromphenol, and, by further action, trichlorand tribrom-phenol.

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  • lodphenol is obtained by the action of iodine a.nd iodic acid on phenol dissolved in a dilute solution of caustic potash.

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  • Nitro-phenols are readily obtained by the action of nitric acid on phenol.

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  • By nitrating phenol with concentrated nitric acid, no care being taken to keep the temperature of reaction down, trinitrophenol (picric acid) is obtained (see Picric Acid).

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  • Phenol dissolves readily in concentrated sulphuric acid, a mixture of phenol-orthoand -para-sulphonic acids being formed.

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  • A thiophenol, C 6 H 5 SH, is known, and is prepared by the action of phosphorus pentasulphide on phenol, or by distilling a mixture of sodium benzene sulphonate and potassium sulphydrate.

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  • Various methods have been devised for the quantitative determination of phenol.

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  • Vortmann (Ber., 1890, 23, p. 2 753) dissolve phenol in caustic alkali, make the solution up to known volume, take an aliquot part, warm it to 60° C., and add decinormal iodine solution until the liquid is of a deep yellow colour.

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  • Industry, 1899, 18, p. 553) adds excess of sodamide to a solution of the phenol in a suitable solvent, absorbs the liberated ammonia in an excess of acid, and titrates the excess of acid.

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  • When fused with caustic potash it yields phenol and salicylic acid.

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  • Xanthene, C13H100, may be synthesized by condensing phenol with ortho-cresol in the presence of aluminium chloride.

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  • In the first thesis, phenol or oxybenzene,C 6 H 5.

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  • These three acids yield on heating phenol, identical with the substance started with, and since in the three oxybenzoic acids the hydroxyl groups must occupy positions other than I, it follows that four hydrogen atoms are equal in value.

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  • Substitution of the Benzene Ring.-As a general rule, homologues and mono-derivatives of benzene react more readily with substituting agents than the parent hydrocarbon; for example, phenol is converted into tribromphenol by the action of bromine water, and into the nitrophenols by dilute nitric acid; similar activity characterizes aniline.

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  • Doebner's preparation of mesotartaric acid, the internally compensated tartaric acid, (CH(OH) COOH)21 by oxidizing phenol with dilute potassium permanganate (Ber., 1891,.

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  • Potassium chlorate and hydrochloric acid oxidize phenol, salicylic acid (o-oxybenzoic acid), and gallic acid ([2.3.4] trioxybenzoic acid) to tri chlorpyroracemic acid (isotrichlorglyceric acid), CC13 C(OH)2 C02H, a substance also obtained from trichloracetonitrile, CC1 3 CO CN, by hydrolysis.

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  • CC13+C02 O?OIi O / O / (4) Cl2HC CO CHCl2+CH302C CCl2C02CH3 (5) Cl2HC CONH2 Cl (z) (2) When phenol is oxidized in acid solution by chlorine, tetrachlorquinone is obtained, a compound also obtainable from hydroquinone.

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  • When thus chlorinated phenol (I) yields trichlor-o-diketo-R-hexene (2), which may be hydrolysed to an acid (3), which, in turn, suffers rearrangement to trichlor-R-pentene-oxycarboxylic acid (4).

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  • Succinosuccinic ester behaves both as a ketone and as a phenol, thereby exhibiting desmotropy; assuming the ketone formula as indicating the constitution, then in Baeyer's equation we have a migration of a hydrogen atom, whereas to bring Ladenburg's formula into line, an oxygen atom must migrate.

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  • 26, water 3.81-2.32; phenol, nitric acid, sulphuric acid, nitroethane, and propionitril, also exhibit association.

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  • This holds for benzene and phenol, and is supported by the observations of Gossner on [1.3.5] trinitrobenzene and picric acid (1.3.5-trinitro, 2 oxybenzene); these last two substances assume rhombic forms, and picric acid differs from trinitrobenzene in having w considerably greater, with x and slightly less.

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  • It may be obtained by the oxidation of saligenin and of salicylic aldehyde; by the distillation of copper benzoate; by the decomposition of anthranilic acid with nitrous acid; by fusion of ortho-chlor or ortho-brom benzoic acid with potash; by heating orthocyanphenol with alcoholic potash; by heating a mixture of phenol, carbon tetrachloride and alcoholic potash to 100° C. (F.

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  • Reimer, Ber., 1876, 9, p. 1285); and by the action of sodium on a mixture of phenol and chlorcarbonic ester (T.

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  • Sodium phenolate is heated in a stream of carbon dioxide in an iron retort at a temperature of 180-220° C., when half the phenol distils over and a basic sodium salicylate is left.

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  • Manasse (German patent 73,279) prepared an intimate mixture of phenol and potassium carbonate, which is then heated in a closed vessel with carbon dioxide, best at 130 -160 C. The Chemische Fabrik vorm.

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  • Hofmann and Schotensack decompose a mixture of phenol (3 molecules) and sodium carbonate (4 mols.) with carbonyl chloride at 140-zoo° C. When 90% of the phenol has distilled over, the residue is dissolved and hydrochloric acid added, any phenol remaining is blown over in a current of steam, and the salicylic acid finally precipitated by hydrochloric acid.

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  • It sublimes, but on rapid heating decomposes into carbon dioxide and phenol.

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  • It yields both esters and ethers since it is an acid and also a phenol.

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  • When boiled with aniline it gives methylaniline and phenol.

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  • Phenyl salicylate, C6H4(OH) C 02C6H5, or salol, is obtained by heating salicylic acid, phenol and phosphorus oxychloride to 120-125° C.; by heating salicylic acid to 2 =0° C.; or by heating salicyl metaphosphoric acid and phenol to 140-150° C. (German Patent 85,565).

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  • When heated in air for many hours it decomposes, yielding carbon dioxide, phenol and xanthone.

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  • It is usually prepared by the so-called "Reimer" reaction (Ber., 1876, 9,p. 1268), in which chloroform acts on phenol in the presence of a caustic alkali, C 6 H 5 OH+CHC1 3 +4KHO = 3KCI+3H20+KO�C6H4�CHO, some para-oxybenaldehyde being formed at the same time.

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  • The latter on reduction yields a diamino compound, the disulphonic acid of which on diazotization and coupling with a phenol, &c., gives valuable substantive cotton dyes after the type yielded by Benzidine.

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  • It solidifies in a freezing mixture, on the addition of a crystal of phenol, and then melts at 3 0 -4° C. It boils at 202° 8 C. Its aqueous solution is coloured bluish-violet by ferric chloride.

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  • The secondary amines may be of two types-namely,the purely aromatic amines, and the mixed secondary amines, which contain an aromatic residue and an alkyl group. The purely aromatic amines result upon heating the primary amines with their hydrochlorides, and, in some cases, by heating a phenol with a primary amine and anhydrous zinc chloride.

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  • Picric acid can also be obtained from it by first treating acetylene with sulphuric acid, converting the product into phenol by solution in potash and then treating the phenol with fuming nitric acid.

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  • soc. chim., 18 94 (3) 11, p. 1129) obtained anilino-derivatives of the paraquinones by the action of an aqueous solution of potassium chromate on an acetic acid solution of para-aminodimethylaniline and phenol: C 6 H 5 OH+H 2 N C 6 H 4 N (CH 3) 2 - *O:C 6 H 4 :N C 6 H 4 N(CH 3) 2; these compounds yield the quinone when heated with mineral acids.

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  • They may be prepared by the reduction of nitro compounds in alkaline solution (using zinc dust and alkali, or a solution of an alkaline stannite as a reducing agent); by oxidation of hydrazo compounds; or by the coupling of a diazotized amine and any compound of a phenolic or aminic type, provided that there is a free para position in the amine or phenol.

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  • The oxyazo compounds are prepared by adding a solution of a diazonium salt to a cold slightly alkaline solution of a phenol.

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  • Para-oxyazobenzene (benzene-azo-phenol), C 6 H 5 N: N (1) C6H4 011(4), is prepared by coupling diazotized aniline with phenol in alkaline solution.

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  • The more complete phenomena of mutual solubility are illustrated by the case of phenol and water.

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  • 4 A represents the freezing point of pure water, and AB the freezing point curve showing the depression of the freezing point as phenol is added.

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  • At B is a nonvariant system made up of ice, solid phenol, saturated solution and vapour.

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  • BCD c is the solubility curve of phenol in water.

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  • At C a new o° A C liquid phase appears - the B solution of water in liquid ' r q Ivater 50 Phenol phenol, the solubility of which FIG.

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  • Replacement of -NH 2 by-OH:-The amine is diazotized and the aqueous solution of the diazonium salt is heated, nitrogen being eliminated and a phenol formed.

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  • It may be condensed to a liquid, which boils at about o° C. It is a powerful methylating agent, reacting with water to form methyl alcohol, and converting acetic acid into methylacetate, hydrochloric acid into methyl chloride, hydrocyanic acid into acetonitrile, and phenol into anisol, nitrogen being eliminated in each case.

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  • PICRIC ACID, or [[Trinitrophenol, C6h2 Oh]] (N02)3 [5.2.4.6], an explosive and dyestuff formed by the action of concentrated nitric acid on indigo, aniline, resins, silk, wool, leather, &c. It is the final product of the direct nitration of phenol, and is usually prepared by the nitration of the mixture of phenol sulphonic acids obtained by heating phenol with concentrated sulphuric acid (E.

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  • Pasteur, Ann., 1853, 88, p. 212); by heating tartaric or racemic acid for some time with water to 165° C.; by the oxidation of laevulose; and by the oxidation of phenol or maleic acid with an alkaline solution of potassium permanganate (0.

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  • It may be prepared synthetically by fusing meta-iodophenol, phenol meta-sulphonic acid, and benzene meta-disulphonic acid with potash; by the action of nitrous acid on meta-aminophenol; or by the action of 10% hydrochloric acid on meta-phenylene diamine (J.

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  • (2) Argenti oxidum, incompatible with chlorides, organic substances, phenol, creosote, &c., with which it forms explosive compounds.

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  • Benzidine finds commercial application since its tetrazo compound couples readily with amino-sulphonic acids, phenol carboxylic acids, and phenol and naphthol-sulphonic acids to produce substantive cotton dyes (see Dyeing).

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  • Carum copticum, from which it may be extracted by shaking with potassium hydroxide, filtering and precipitating the phenol with hydrochloric acid.

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  • Cyclo-hexanone, C 6 H 10 0, is obtained by the distillation of calcium pimelate, and by the electrolytic reduction of phenol, using an alternating current.

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  • The acid (and anhydride) are largely used in the colour industry (see Fluorescein; Phenol Phthalein) .

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  • Hypochlorous acid gives para-amino phenol and para-amino diphenylamine (E.

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  • Investigations in phenol formaldehyde resins for example elucidate mechanism and provide new flame retardant materials.

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  • Phenol tends to burn in air with an extremely smoky flame - full of carbon particles.

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  • Isolated in such blocks the selected prisoner perished either from hunger or from an injection of phenol or were suffocated by gas.

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  • During the 1920's and 1930's, a researcher named Arthur Penfold studied tea tree oil and discovered that the oil was eleven times more active than phenol (carbolic acid).

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  • Phenols, specifically Nonyl phenol ethoxylate - Per the National Institutes of Health, phenol is toxic.

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  • Alcohol and phenol are injected in combination but are less commonly used to treat spasticity.

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  • Short-term medications such as lidocaine, a local anesthetic, can be used to assess the potential benefit of botulinum toxin or alcohol and phenol injections.

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  • Over-the-counter lip products that contain the chemical phenol (such as Blistex Medicated Lip Ointment) and numbing ointments (Anbesol) help to relieve cold sores.

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  • Alcohol or phenol injections into the nerve controlling the muscle are another option.

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  • Irritant dermatitis is essentially a direct injury to the skin, caused by such compounds as acids, alkalis, phenol, and detergents.

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  • Alcohol and phenol are injected in combination, but are less common treatments.

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  • Short-term medications such as lidocaine, a local anesthetic, can be used to assess the potential benefit of botulinum-toxin or alcohol and phenol injections.

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  • The Bean mat contains no phthalates, dioxins, furans, phenol, or heavy metals, has an ecologically safer method of production, and is available for under $15.

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  • Chemical peel kits can contain salicylic acid, resorcinol, sulfur, PPT, and/or phenol.

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