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A Manual of the Chemistry of the Carbon Compounds

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376 THE CHEMISTRY OF<br />

isoxylene, by dissolving <strong>the</strong> hydrocarbon in cold, fuming nitric acid<br />

It in a pole-yellow liquid, boiling at 239°,<br />

pinitro-wxylene C^H^NOACCHj)^ crystallizes from alcohol in long<br />

brilliant prisms, melting at 93 .<br />

Trinitro-isoxylene C0H(NOJ)8(CHJ)8 forms colourless crystals, melting<br />

at 177°.<br />

Amido-isoxylme CaH,(fTH3)(CH8)i is a colourless liquid, boiling at<br />

216°, and forming crystallizable salts.<br />

ORTHOXYJLENE, OR 1*2 DIMETHYL-TOLUENE.<br />

This hydrocarbon has been obtained by distilling paraxylio acid<br />

e H/OH^COH / ^ j with lime. It is a liquid, q , boiling g at 140°, , and<br />

possessing a peculiar, li unpleasant l t odour. d It does d not form f readily dil<br />

solid nitro-conipounds.<br />

XYLKNOIS,<br />

lsozylenol C6BL(OH)(CHg)y—When mesitylenesulphonic acid is<br />

heated with potash to 250°, it is converted into oxymesitylenie acid,<br />

which, by heating <strong>the</strong> fused mass to 290°, is changed into isoxylenol;<br />

(1) CftfCH^K + 3KOH „ C6H2(CH3)a jg*^ + 3HaO<br />

(2) C,H,(Cfl^ { °*K + KOH = C6H8(CHSXOK + K,COS<br />

It is a crystalline solid, melting at 75°, and boiling at 216°.<br />

By dissolving crude xylene in sulphuric acid, and fusing <strong>the</strong><br />

xylenesulphonic acid with caustic potash, two xylenols are obtained;<br />

one seems to be identical with that obtained from mesitylene, and <strong>the</strong><br />

o<strong>the</strong>r is a colourless, strongly refraotive liquid, hoiling at 211 O *5,<br />

Phlorone, or Xyloyrimm 0JB,^GH^«O« is produced by treating<br />

coaltar-oil or creosote, boiling above 210 , with manganese dioxide<br />

and sulphuric acid. It forms golden-yellow, oblique, rhombic prisms;<br />

on heating, it gives <strong>of</strong>f a very pungent smell, which attacks violently<br />

<strong>the</strong> eyes and mucous membranes. It is soluble in boiling water,<br />

and sublimes on heating.<br />

Hydrophiorom, or Xylohydroquinme C0H?(CH8)o(OH)a, is obtained<br />

by reducing phlorone with sulphurous acid, and crystallizes from<br />

boiling water in white, pearly scales.<br />

Bctcwrtin CgH^OH),, is obtained from usnic acid, and similar acids<br />

occurring in lichens, by <strong>the</strong> same method by which oroin is prepared<br />

from orseltinio acid. It is soluble in water and alcohol, and crystal-

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