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A Manual of the Chemistry of the Carbon Compounds

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102 TEE CHEMI8THY OF<br />

in sealed tubes for forty-eight hours. It is also readily formed by<br />

heating brom<strong>of</strong>orm -with bromine and iodine. Tetrabromomethane<br />

crystallizes in white shining plates, melting at 91°, and boiling with<br />

slight decomposition at 189-5°.<br />

lod<strong>of</strong>om., Tri-wdomethane CHIy—This compound is formed by<br />

acting with potash or potassium carbonate and iodine upon ethyl<br />

alcohol, aldehyde, acetone, and many o<strong>the</strong>r carbon compounds, but<br />

pure methyl alcohol yields no iod<strong>of</strong>orm. It crystallizes in yellow<br />

scales, emells like saffron, melts at 120°, and is decomposed at a<br />

higher temperature, but may be volatilized in a current <strong>of</strong> steam.<br />

On heating it in a closed tube for some time to 150°, me<strong>the</strong>ne diiodide<br />

or di-iodmnetlianc CH2I2 is formed, a compound which can also<br />

be obtained by heating chlor<strong>of</strong>orm with fuming hydriodic acid:—<br />

CHCls + 4HI = CH2Ig + 3HC1 + I3<br />

This compound is a yellowish heavy liquid, which boils at 181° and<br />

at — 2° solidifies to a crystalline mass.<br />

Nitroehior<strong>of</strong>orm, Nitrotrkhloivmetlmne, or CJdoi-opicrin C(NO2)C1S is<br />

formed when methyl- or ethyl alcohol are distilled with salt, saltpetre,<br />

and sulphuric aeid, and also by <strong>the</strong> distillation <strong>of</strong> many nitro-compounds<br />

with a solution <strong>of</strong> bleaching powder.<br />

It is best prepared by mixing in a still, ten parts <strong>of</strong> bleaching<br />

powder with water to form a paste, and adding one part <strong>of</strong> picric<br />

acid CaH2(N02)sOH; a violent reaction sets in and <strong>the</strong> chloropicrin<br />

distils over. It is a colourless liquid, possessing a most irritating<br />

smell, and boiling at 112°. On distilling it with acetic"acid and ironfilings<br />

it is reduced to methylamine:—<br />

61fa = CH^NH, + SHC1 4 2fla0<br />

Nitr<strong>of</strong>orm, Trinilromctlianc, CHtNO^g.—This body is produced by<br />

decomposing trijiitroacetonilriU C2(NO3)3N (see Fulminates) with<br />

water :—<br />

Nitr<strong>of</strong>orm .is a weak acid; <strong>the</strong> product <strong>of</strong> <strong>the</strong> reaction consists<br />

<strong>the</strong>refore <strong>of</strong> <strong>the</strong> ammonium salt. On acting on trinitroacetonitrile with<br />

caustic potash, tbe potassium salt CKfNO^g is obtained, which forms<br />

yellow crystals. On adding concentrated sulphuric acid to one <strong>of</strong><br />

<strong>the</strong>se salts, nitr<strong>of</strong>orm separates out as a light oily layer, which on<br />

cooling solidifies, forming colourless, cubical crystals. It has an unpleasant<br />

smell and bitter taste, and is highly inflammable, In water<br />

it dissolves with a yellow colour. On quickly heating it or oue <strong>of</strong> its<br />

salts, it decomposes with a violent explosion.<br />

Tetranitromthane (/(NO^.—-By passing a current <strong>of</strong> air through a<br />

solution <strong>of</strong> nitr<strong>of</strong>orm in a mixture <strong>of</strong> concentrated nitric and sulphuric<br />

adds, tetranitromethane distils over:—

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