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A Manual of the Chemistry of the Carbon Compounds

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THE CARBON COMPOUNDS. 101<br />

triad radicals, but as <strong>the</strong>y bear very little relation to o<strong>the</strong>r groups<br />

<strong>of</strong> carbon compounds <strong>the</strong>y will be treated <strong>of</strong> here.<br />

Afe<strong>the</strong>ne BvMoride, Dichkromelhane CILClj can be obtained by <strong>the</strong><br />

action <strong>of</strong> chlorine upon marsh-gas, or by adding hydrochloric acid and<br />

zinc to an alcoholic solution <strong>of</strong> chlor<strong>of</strong>orm. It is a heavy liquid,<br />

smelling like chlor<strong>of</strong>orm and boiling at 41°.<br />

Chlor<strong>of</strong>orm, Trichloromethane CHCL,.—The third substitution product<br />

<strong>of</strong> marsh-gas is also formed by <strong>the</strong> action <strong>of</strong> bleaching powder on<br />

ethyl alcohol, and o<strong>the</strong>r carbon compounds. To prepare it ten parts<br />

<strong>of</strong> bleaching powder are mixed with forty parts <strong>of</strong> hot water in a<br />

large still, and one part <strong>of</strong> spirits <strong>of</strong> wine is added; a reaction soon<br />

sets in by which sufficient heat is evolved to drive <strong>the</strong> chlor<strong>of</strong>orm<br />

over.<br />

Chlor<strong>of</strong>orm is a colourless mobile liquid, possessing a peculiar<br />

sweetish smell and taste. It boils at 62°, and has at 0° <strong>the</strong> specific<br />

gravity 1-525. The inhalation <strong>of</strong> its vapour produces anaes<strong>the</strong>sia,<br />

and it is <strong>the</strong>refore largely employed in surgical operations. It is also<br />

used as a solvent for iodine, bromine, alkaloids, gutta percha, &c.<br />

The smallest quantity <strong>of</strong> chlor<strong>of</strong>orm can be easily detected by<br />

adding to <strong>the</strong> liquid to be tested a monamine (or aniline) and an<br />

alcoholic solution <strong>of</strong> caustic potash. When it is present in larger<br />

quantities <strong>the</strong> peculiar odour <strong>of</strong> <strong>the</strong> carbamines is given <strong>of</strong>f at once,<br />

or after gently heating when only traces are present. Vice versd,<br />

chlor<strong>of</strong>orm can be used for detecting <strong>the</strong> presence <strong>of</strong> a monamine.<br />

TetrachlorometAane, <strong>Carbon</strong> TetrackloruU CCL is best prepared by<br />

acting with chlorine upon chlor<strong>of</strong>orm in <strong>the</strong> sunlight; it may also be<br />

obtained by passing chlorine and carbon disulphide through a porcelain<br />

tube filled with fragments <strong>of</strong> porcelain. It is a heavy liquid, boiling<br />

at IT and possessing <strong>the</strong> odour <strong>of</strong> chlor<strong>of</strong>orm. On heating it with an<br />

alcoholic solution <strong>of</strong> potash it yields potassium chloride, potassium<br />

carbonate, and water :—<br />

CC1, + 6E0H = CO 15J! + 4KC1 + 3HaO<br />

When its vapour mixed with hydrogen is passed through a glasstube<br />

filled with broken glass, and lmted to a dull red beat, hexaeltforethane<br />

CaCl0 is formed :—<br />

2CC1, + H3 = 2HC1 +<br />

Bromqfwm, Tnhrommdlmm CHBr., a liquid resembling chlor<strong>of</strong>orm<br />

and boiling at 152°, is obtained by adding bromine to a solution <strong>of</strong><br />

potash in ethyl alcohol; brom<strong>of</strong>orm very <strong>of</strong>ten occurs in commercial<br />

bromine.<br />

Tetrahwnomethane, <strong>Carbon</strong> Tdrabromide CBr4.—On heating bromine<br />

with carbon disulphide in sealed tubes to 180°, an exceediugly slow<br />

action sets in, which is very much accelerated by adding some iodine.<br />

To prepare tetrabromomethane, two parts <strong>of</strong> carbon disulphide, four,<br />

teen parts <strong>of</strong> bromine, and three parts <strong>of</strong> iodine are heated to 150°

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