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A Manual of the Chemistry of the Carbon Compounds

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368 TEE CHEMISTRY OF<br />

out in colourless prisms. It explodes violently when heated, and is<br />

decomposed by boiling water, 1*3 oxybenzoic acid being formed :—<br />

The free acid is obtained by adding an alkali to a solution <strong>of</strong> <strong>the</strong><br />

nitrate; it is a yellow body, which soon undergoes spontaneous decomposition<br />

Dum-amidobemnc Acid C0H4 j gjj^H)QlHrCOiH ifJ preeipitated<br />

in orange crystals by adding aniidobenzoio acid to an aqueous solution<br />

<strong>of</strong> diazobemoic acid, It is almost insoluble in water, and a bibasic<br />

acid. When heated, it is decomposed with a slight explosion.<br />

UramidobmzoieAdd C6H4 j gJ^ 0NH 2_This compound is distinguished<br />

by <strong>the</strong> great number <strong>of</strong> derivatives which it yields. It is<br />

produced by fusing urea with 1'3 amidobenzoic acid, By <strong>the</strong> action<br />

<strong>of</strong> strong nitric acid it yields three isomeric dinitro-acids, which,<br />

owing to tbo great similarity <strong>of</strong> <strong>the</strong>ir properties, cannot be separated<br />

from each o<strong>the</strong>r.<br />

When an ammoniacal solution <strong>of</strong> <strong>the</strong>se acids is boiled, <strong>the</strong>y are converted<br />

into <strong>the</strong> mononitro-acids;—<br />

N( V° H<br />

The mononitro-com pounds can easily be separated, <strong>the</strong>ir barium<br />

salts possessing a very different solubility in water. On acting with<br />

nitric acid on <strong>the</strong> pure mononitro-acids, <strong>the</strong> dinitro-acids are obtained<br />

perfectly pure. They form yellowish-white needles, and are freely<br />

soluble in alcohol, but scarcely soluble in water. By boiling <strong>the</strong>m<br />

with water for a long time, <strong>the</strong>y are converted into amido-nitrobenzoie<br />

acids}—<br />

WNO^-J ^H° N H 2 = CATO { g ^ + COa + NaO<br />

When <strong>the</strong>se amido-nitro-acids are gently heated with tin and<br />

hydrochloric acid, <strong>the</strong>y are reduced to diamidobenzoic acids,<br />

a Diamidobenzoic Acid C8H8 -I QQ j¥ a " 8 P ar "igly soluble in hot<br />

water, and forms minute prisms, lte sulphate CgHgCCOgHXNH^aSO^a<br />

is almost insoluble in water. On distilling <strong>the</strong> acid, it is resolved in<br />

carbon dioxide and orthodiamidobenzene (see page 327),<br />

0 JXamidobenzwc Acid is more freely soluble, and crystallizes in<br />

pale-yellow plates. The sulphate has <strong>the</strong> composition 2[06Hs(C03H)<br />

(NH2}JSO4H2, and is more soluble than <strong>the</strong> a compound

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