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A Manual of the Chemistry of the Carbon Compounds

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336 THE CHEMISTRY OJP<br />

water, and crystallizes in long, shining yellow needles; by heat and<br />

by percussion it explodes with an extraordinary violence, and is<br />

<strong>the</strong>refore used for <strong>the</strong> preparation <strong>of</strong> explosives,<br />

The picrates <strong>of</strong> sodium, ammonium, barium, and silver are readily<br />

soluble in. water.<br />

Ethyl pkrate CjH^NO^OCgHj is produced by <strong>the</strong> action <strong>of</strong> ethyl<br />

iodide upon dry silver picrate. It crystallizes in long, pale-yellow<br />

needles, which oa heating first melt, and <strong>the</strong>n decompose with a<br />

slight explosion.<br />

By <strong>the</strong> action <strong>of</strong> phosphorus pentacbloride upon picric acid, triniirocMorobenzene<br />

CjHiNOjJgCl is obtained, a crystalline solid, having<br />

an aromatic smelL Ihis compound has been also called picryl chloride,<br />

because it is decomposed by water, analogous to o<strong>the</strong>r acid chlorides,<br />

into picric acid and hydrochloric acid.<br />

This reaction shows how <strong>the</strong> character <strong>of</strong> an aromatic compound is<br />

modified when hydrogen is replaced by nifcroxyL Whilst monochlorobenzene<br />

is not acted on by caustic potash, its trinitro-couipound<br />

is readily decomposed by water.<br />

Ttimlro-amidobanzene, or JHeramide CjHJNO-JgBHj, is produced<br />

by acting with ammonium carbonate on picryl chloride, or by heating<br />

ethyl picrate with alooholic ammonia. It crystallizes from glacial<br />

acetic acid in glistening yellow plates, melting at 187°. On heating<br />

it stronger, it decomposes without explosion ; and, by boiling it with<br />

caustic potash, it yields ammonia and potassium picrate.<br />

Picric acid combines with aromatic hydrocarbons, forming compounds<br />

which are distinguished by <strong>the</strong>ir characteristic colours<br />

or crystalline forms. This acid is, <strong>the</strong>refore, <strong>of</strong>ten used for <strong>the</strong><br />

detection or separation <strong>of</strong> such hydrocarbons. Thus on dissolving<br />

picric acid in not benzene, <strong>the</strong> compound C6H0 -f- C0H2(NOg).OH<br />

separates out on ocoling in pale-yellow transparent crystals, melting<br />

at 149°; it dissolves, without decomposition, in alcohol and e<strong>the</strong>r;<br />

but when exposed to <strong>the</strong> air, benzene is slowly given <strong>of</strong>f, whilst;<br />

alkalis decompose it at once,<br />

Isopurpitric Add, or Picramjamie Add CQHJNJO,.—The potassium<br />

salt <strong>of</strong> this acid is formed by dissolving picric acid in a solution <strong>of</strong><br />

potassium cyanide -,—<br />

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