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A Manual of the Chemistry of the Carbon Compounds

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344 THE CHEMISTRY OF<br />

oxygen from a mixture <strong>of</strong> gases, but it is not adapted for a quantitative<br />

determination <strong>of</strong> oxygen, because <strong>the</strong>re is always a small quantity <strong>of</strong><br />

carbon monoxide formed at <strong>the</strong> same time. By boiling it -with concentrated<br />

caustic potash, it is decomposed into acetic acid, oxalic<br />

acid, and carbon dioxide. The salts <strong>of</strong> silver, gold, &c, are reduced<br />

to <strong>the</strong> metallic state by pyrogallic acid.<br />

By <strong>the</strong> action <strong>of</strong> acetyl chloride on pyrogallol, triawtyl-jryrogaUol<br />

C6H8(O.CaH3O)2 is obtained, a white crystalline solid; and by acting<br />

on pyrogallol with bromine, it yields tribrmopyrogallol C6Br8(OH)g,<br />

separating from alcohol in large colourless crystala<br />

roH<br />

Phloroghcin CMA Off is produced by fusing phloretin, quercitrin,<br />

{ OH<br />

or maclurin (see Glucosides) with caustic potash; and is also obtained<br />

by <strong>the</strong> same reaction from kino, dragon's-blood, gamboge, &c. It<br />

crystallizes from an aqueous solution in large rhombic prisms, containing<br />

two molecules <strong>of</strong> water, and possessing a sweet taste. The<br />

anhydrous compound melts at 220°, and sublimes, when heated more<br />

strongly. It forms deliquescent salts with alkalis, and reduces alkaline<br />

copper-solutions. Ferric chloride imparts to its aqueous solution<br />

a deep-violet colour. By treating it with acetyl chloride, it is converted<br />

into triaedyl-pMoroglucin CjH^O.CgHgO)^ which crystallizes<br />

in small prisms. By adding bromine-water to an aqueous solution <strong>of</strong><br />

phloroglucin, a precipitate <strong>of</strong> tribronwpMoroglvdn C6Br8(OH). is<br />

produced, which crystallizes in long needles. By <strong>the</strong> action <strong>of</strong> dilute<br />

nitric acid, it is converted into nitrojphloroglucin C6Ha.NO3(OH)8,<br />

crystallizing in small reddish-yellow plates. When phloroglucin is<br />

dissolved in ammonia, phloramine or wmidophloroqlucin CaHs(NHj)-<br />

(OH)3 is formed, which is not freely soluble in alcohol, and crystallizes<br />

in small thin plates, resembling mica; it is a base, forming crystalline<br />

salts.<br />

(OH<br />

Filicic Acid, or JHhityryl-pMorogluein CjHg-J J OCOC4HjO,<br />

occurs in<br />

(.0C4Hr0<br />

<strong>the</strong> root <strong>of</strong> <strong>the</strong> male fern (AspiMum Mix-mas), and is deposited<br />

from <strong>the</strong> e<strong>the</strong>rial extract <strong>of</strong> this root in crystals. On fusing it with<br />

caustic potash, it is resolved jnto butyric acid and phloroglucin.<br />

METALUC PE1UVAT1VES OK BBMZENE.<br />

Memiry-diphenyl ^ a ^ j Hg is formed by <strong>the</strong> action <strong>of</strong> sodium<br />

amalgam on bromobenzene. It is insoluble iu water, and crystallizes<br />

from benzene in long colourless prisms, melting at 120°, A small<br />

quantity may be snblimed by heating it carefully; but on heating a<br />

larger quantity to above 300°, decomposition sets in; and benzene,<br />

diphenyl, carbonaceous matter, and free mercury are formed. By <strong>the</strong>

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