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A Manual of the Chemistry of the Carbon Compounds

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THE CARBON COMPOUNDS 317<br />

each. By <strong>the</strong> action <strong>of</strong> alcoholic potash, hydrochloric aoid is taken<br />

out, and chlore<strong>the</strong>ne C2H3Cl is formed, in which <strong>the</strong> carbon-atoms<br />

are again licked toge<strong>the</strong>r, as in e<strong>the</strong>ne.<br />

Hydrogen can also combine with aromatic hydrocarbons, but only<br />

with those containing alcohol-radicals. The number <strong>of</strong> atoms <strong>of</strong><br />

hydrogen combining with <strong>the</strong> hydrocarbon appears to depend, not<br />

only on <strong>the</strong> number <strong>of</strong> <strong>the</strong>se radicals, but also on <strong>the</strong> relative<br />

positions.<br />

To obtain <strong>the</strong>se additive products, <strong>the</strong> hydrocarbon is heated in<br />

sealed tubes with phosphouiutn iodide (a compound <strong>of</strong> liydriodic aoid<br />

with hydrogen phosphide). The hydriodic acid is <strong>the</strong> reducing agent,<br />

being decomposed into hydrogen and iodine, which latter is immediately<br />

acted upon by <strong>the</strong> hydrogen phosphide, and again converted<br />

into hydriodic acid; this change going on until at last only phosphorus<br />

iodide and red phosphorus are left behind.<br />

By subjecting benzene to this reaction, it is not changed even at<br />

350. Methyl-benzene combines with two atoms <strong>of</strong> hydrogen,<br />

and forms <strong>the</strong> hydrocarbon C6H,.CH8, Dimethyl-benzene takes up<br />

four atoms <strong>of</strong> hydrogen, yielding C9Hg| ^^, and trimethyl-benzeue<br />

combines with six atoms <strong>of</strong> hydrogen, forming <strong>the</strong> compound<br />

(CH<br />

There exist also aromatic acids which will combine with hydrogen<br />

in <strong>the</strong> nascent state.<br />

COMPOUNDS WITH SIX ATOMS OP CARBON.<br />

BENZENE j , ,<br />

Benzene, or Benzol, is a colourless, strongly refractive, and mobile<br />

liquid, boiling at 81°, aud solidifying at 0°, to colourless crystals. It<br />

has a density <strong>of</strong> 0*899 at 0°, aud <strong>of</strong> 0-878 at 20°, and a peculiar<br />

aromatic odour. It is very inflammable, burning with a very luminous<br />

and very smoky flame. It is almost insoluble in water, but<br />

dissolves freely in alcohol and e<strong>the</strong>r. It dissolves iodine, sulphur,<br />

phosphorus, fats, resins, and many o<strong>the</strong>r compounds, which are<br />

insoluble or only sparingly soluble in water and alcohol; and hence<br />

it is used for preparing or purifying many compounds.<br />

Benzene has beeu produced artificially from its elutneute. When<br />

acetylene, which, us we have seen (page 274), may be formed by <strong>the</strong><br />

direct combination <strong>of</strong> carbon with hydrogen, is heated in a long,<br />

narrow, bent bell-jar to a temperature at which <strong>the</strong> glass begins to

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