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A Manual of the Chemistry of the Carbon Compounds

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THE CARBON COMPOUNDS. 283<br />

pyrrolic acid C^B^NO., which is obtained as a white flocculent precipitate<br />

on adding hydrochloric acid to <strong>the</strong> solution; it crystallizes<br />

from alcohol in white prisms, and sublimes at 190° in small fea<strong>the</strong>ry<br />

crystals. At a high temperature it is resolved into carbon dioxide<br />

and pyrrol, which is also readily obtained by heating ammonium<br />

pyromucate with glycerin, Pyrrol is a colourless oil, when freshly<br />

prepared, but it soon assumes a brown colour; it boils at 133°, and<br />

possesses a pleasant smell. Pyrrol has <strong>the</strong> characteristic property <strong>of</strong><br />

imparting a fine crimson colour to pine-wood, moistened with hydrochloric<br />

acid. This pyrrol4ed has <strong>the</strong> empirical formula C^B^Oj; it<br />

is also obtained as an amorphous precipitate by heating pyrrol with<br />

an excess <strong>of</strong> hydrochloric acid, and by <strong>the</strong> action <strong>of</strong> acids on tetraphenol<br />

and furfuryl alcohol.<br />

Potassium dissolves in pyrrol with evolution <strong>of</strong> hydrogen, potassium-pyrrol<br />

CJLKN being formed, which, with ethyl iodide, yields<br />

dhyl-pyrrol CgH^C^JN, a colourless liquid smelling like turpentine;<br />

its vapour colours pinewood, moistened with hydrochloric acid<br />

like pyrrol.<br />

The constitution <strong>of</strong> <strong>the</strong> compounds derived from mucic acid is not<br />

exactly kno-wnj <strong>the</strong> relation between <strong>the</strong>m may be expressed by <strong>the</strong><br />

following formula! :—<br />

Adipic Acid. Mucic Acid. Pyromudc Acid.<br />

C « H a{cO.OH 0 * H «( OH )*{co:OH C4H3O.CO.OH<br />

Cnrboyyrrolamide. Carbopyirolic Acid. Pyrrol.<br />

C4H3(NH)CO.NH8 C4H8(NH)CO.OH C4H4.NH<br />

CHELIDONIC ACID AND MECONIC ACID.<br />

Chdidmiic Add CJIfCO.OH)^—This tribasic acid occurs, toge<strong>the</strong>r<br />

with malic acid, in Cliclidoninm wuytavaud is obtained by heating <strong>the</strong><br />

jnice <strong>of</strong> this herb to <strong>the</strong> boiling-point, filtering and acidifying <strong>the</strong><br />

liquid with nitric ncid, Ou adding lead-nitrate, a crystalline precipitate<br />

<strong>of</strong> lead, chelidonate, is formed, which is decomposed by hydrogeo<br />

sulphide. Chelidonic acid is sparingly solnble in cold, bnt readily in<br />

hot water, and crystallizes in colourless needles. By <strong>the</strong> action <strong>of</strong><br />

bromine it is decomposed, yielding brom<strong>of</strong>orm and pentahvmacetone<br />

CsHBr6O.<br />

Meeonic acid C4HO(CO.OH)3 is foand in combination with morphine<br />

and o<strong>the</strong>r bases in opium; its calcium salt is obtained as a byproduct<br />

in <strong>the</strong> manufacture <strong>of</strong> <strong>the</strong>se alkaloids, On decomposing this<br />

salt with hydrochloric acid, impure ineconic acid separates out, which<br />

is purified by converting it into <strong>the</strong> ammonium salt, which is crystallized,<br />

and <strong>the</strong>n again decomposed with hydrochloric acid.<br />

Meconic acid crystallizes from a hot aqueous solution in scales or

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