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A Manual of the Chemistry of the Carbon Compounds

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THE CARBON COMPOUNDS. 445<br />

from hot benzene in hard, colourless needles. By <strong>the</strong> action <strong>of</strong> heat<br />

it is resolved into bromine, hydrobromic acid, and tribi'omantkracene<br />

Clt,B8<br />

Tekabromanthraccne CuH0Br4 is a body resembling <strong>the</strong> di- and<br />

tri-bromo-eompound, and obtained by <strong>the</strong> action <strong>of</strong> hot alcoholic<br />

potash on dibroinanthracene tetrabromide.<br />

MITJtO- AND AMID0-C0MFOUNDS.<br />

These compounds are but little known; dilute, as well as concentrated<br />

nitric acid, converts anthracene into antliraquinone, but by <strong>the</strong><br />

action <strong>of</strong> nitric acid on an alcoholic solution <strong>of</strong> anthracene <strong>the</strong> following<br />

nitro-compounds have been obtained.<br />

Bed Nitro-anthraeene O^HjNOg is insoluble in cold alcohol, and<br />

crystallizes from hot alcohol in red needles. When treated with tin<br />

and hydrochloric neid, it yields iso-anthracene and amido-anthracene<br />

CuH0.NH2, which is precipitated by alkalis in yellow flakes; it is a<br />

very unstable body, turning rapidly brown in <strong>the</strong> air. It dissolves<br />

acids, but does not form definite salts.<br />

White Nitro-anthracenc is more freely soluble in alcohol than <strong>the</strong><br />

red compound, and readily in benzene, from which it crystallizes in<br />

colourless needles.<br />

Dinitro-anthraccne C14H8(NO4) is readily soluble in hot alcohol<br />

and benzene, and sublimes in small colourless plates.<br />

Isonitro-atUhracene C^H^NOj ha3 been obtained by boiling isoanthracenc<br />

with nitric acid; it is sparingly soluble in alcohol, freely<br />

in benzene, and sublimes in pale-yellow needles, melting at 209°.<br />

ANTHRACENESULPHOX1C ACIDS.<br />

AnthraccncmonomlpJiomc Acid CuHj.SOsH is formed by dissolving<br />

anthracene in concentrated sulphuric acid at 100°; ita lead salt<br />

crystallizes in yellowish-white prisms, having <strong>the</strong> composition<br />

(CuH0.SQ,)2Pb, By heating anthracene with sulphuric acid to 150°,<br />

<strong>the</strong> disulphonic acid is produced.<br />

Dichloranthracmcdisulphonic Add CuH0Clo(S08H)? is obtained by<br />

heating dichlorantfiracenc with fuming sulphuric acid on a water*<br />

bath. It forms orange-yellow crystals, which are solnble in water,<br />

but not in dilute acids.<br />

ANTHRAQUHiONE, OK OXYANTHRACENE CUH8O&<br />

Tliis compound is readily obtained by boiling anthracene with<br />

dilute sulphuric acid and potassium dichromate, or with nitric acid.<br />

It crystallizes from hot nitric acid in pale-yellow needles, melting at

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