Carboxylic-acid sentence example

carboxylic-acid
  • 7-dihydroxyxanthone, known as euxanthone, is prepared by heating euxanthic acid with hydrochloric acid or by heating hydroquinone carboxylic acid with 3-resorcylic acid and acetic anhydride (S.
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  • 7-trihydroxyxanthone, is found in the form of its methyl ether (gentisin) in gentian root; it is obtained synthetically by condensing phloroglucin with hydroquinone carboxylic acid.
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  • An a-pyrrolidine carboxylic acid and its hydroxy derivatives have been detected by E.
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  • Potassium persulphate oxidizes it in alkaline solution, the product on boiling with acids giving hydroquiirone carboxylic acid (German Patent 81,297).
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  • It is the carboxylic acid corresponding to tropine, for it yields the same products on oxidation, and by treatment with phosphorus pentachloride is converted into anhydroecgonine, C9H13N02, which, when heated to 280° C. with hydrochloric acid, splits out carbon dioxide and yields tropidine, C8H13N.
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  • On oxidation .ith chromic acid it forms a quinone, C 15 H 8 0 2, and an a-diphenylene keto carboxylic acid C E I-4 3.
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  • Duppa in 1865 examined the reaction and concluded that Geuther's sodium salt was a derivative of the ethyl ester of acetone carboxylic acid and possessed the constitution CH3CO�CHNa�OOOC2H5.
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  • a little hydrochloric acid, methylene diresorcin [(HO) 2 C 6 H 3] 2 CH 2, whilst with chloral hydrate, in the presence of potassium bisulphate, it yields the lactone of tetra-oxydiphenyl methane carboxylic acid (J.
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  • Cyclo-heptanone (suberone), C 7 H 12 O, is formed on the distillation of suberic acid with lime, and from a-brom-cyclo-heptane carboxylic acid by treatment with baryta and subsequent distillation over lead peroxide (R.
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  • Cyclo-heptane carboxylic acid (suberanic acid), C7H13C02H, is obtained by the reduction of cyclo-heptene-I-carboxylic acid; from brom-cyclo-heptane by the Grignard reaction; and by the reduction of hydrotropilidine carboxylic acid by sodium in alcoholic solution (R.
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  • Amino-cyclo-heptane (suberylamine) is obtained by the reduction of suberone oxime or by the action of sodium hypobromite on the amide of cycloheptane carboxylic acid.
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  • Adding an acid such as hydrochloric acid or sulphuric acid to the sodium carboxylate would free the carboxylic acid.
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  • esterify mentioned in Chapter 20 that an alcohol can be esterified with an inorganic acid just as well as with a carboxylic acid.
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  • hydrolysis of a nitrile produces a carboxylic acid ' .
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  • An example of such a system is the nucleation of calcite crystals on carboxylic acid terminated alkyl thiols, which produces highly oriented crystals.
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  • It is the carboxylic acid corresponding to tropine, for it yields the same products on oxidation, and by treatment with phosphorus pentachloride is converted into anhydroecgonine, C9H13N02, which, when heated to 280° C. with hydrochloric acid, splits out carbon dioxide and yields tropidine, C8H13N.
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  • Duppa in 1865 examined the reaction and concluded that Geuther's sodium salt was a derivative of the ethyl ester of acetone carboxylic acid and possessed the constitution CH3CO�CHNa�OOOC2H5.
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  • When digested with fuming hydrochloric acid for some time it is converted into ad furfurane dicarboxylic acid (see Furfurane); while on heating with barium sulphide it is transformed into a - thiophene carboxylic acid (see Thiophene).
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  • Gabriel), /CH= C C 6 H 5 CH= C C,H5 -->C6H4 -*C 6 H4C I -?C,H4< I CC1=N CH=N and from isocoumarin carboxylic acid by conversion into isocarbostyril on heating, and subsequent reduction by distillation with zinc dust (E.
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