19.06.2013 Views

A Manual of the Chemistry of the Carbon Compounds

A Manual of the Chemistry of the Carbon Compounds

A Manual of the Chemistry of the Carbon Compounds

SHOW MORE
SHOW LESS

Create successful ePaper yourself

Turn your PDF publications into a flip-book with our unique Google optimized e-Paper software.

00 THE CHEMISTRY OF<br />

cyanate with dilute sulphuric acid, but a part <strong>of</strong> <strong>the</strong> acid easily<br />

undergoes a change by taking water up and forming ammonia and<br />

carbon oxysulphide COS, a decomposition analogous to <strong>the</strong> formation<br />

<strong>of</strong> ammonia and carbon dioxide from cyanic acid. By adding<br />

ferric chloride to a solution <strong>of</strong> snlphocyanic ncid or a sulphocyanate<br />

<strong>the</strong> liquid assumes a deep blood-red colour. This very characteristic<br />

reaction is caused by <strong>the</strong> formation oifcrrie sulpluxyanidc ^ -*'* [ So,<br />

a salt which may be obtained in small blackish red crystals on evaporating<br />

a solution <strong>of</strong> ferric hydroxide in sulphocyanic acid.<br />

Gyanogcn Sulphide Q-M- J- S, is formed by heating a mixture <strong>of</strong><br />

eyanogen iodide and silver sulphocyanate :—<br />

CN) can,, n canl}<br />

+ Ag} S -Ag| + CN} S -<br />

It sublimes in transparent rhombic plates, which smell like<br />

cyanogen iodide, and readily dissolve in water, alcohol, and e<strong>the</strong>r. By<br />

caustic potash it is decomposed thus:—<br />

+2|O= JS+ JO +<br />

I&omtyiliocyaHxtes.—When persulphocyanio acid is treated wi<br />

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

which is obtained by slow evaporation from an aqueous solution in<br />

hard crystals having <strong>the</strong> composition CSNK + H2O. This body may<br />

be easily.'distinguished from potassium snlphocyanate by adding to its<br />

aqueous solution a drop <strong>of</strong> ferric chloride, a brown coloration being<br />

produced, which disappears agnin on adding more <strong>of</strong> <strong>the</strong> ferric salts.<br />

When <strong>the</strong> isosulphocyanate is heated, it melts and undergoes a molecular<br />

change, being transformed into <strong>the</strong> common sulphocyanate.<br />

The free isoswlphocyanic acid has not yet been obtained, but we are<br />

acquainted with a series <strong>of</strong> e<strong>the</strong>rs <strong>of</strong> this acid, <strong>of</strong> which <strong>the</strong> best<br />

known is oil <strong>of</strong> mustard or allyl isosnlphocyanate, having <strong>the</strong> con-<br />

stitutioa N<br />

f<br />

•<<br />

CS<br />

PV , from which it follows that iaosulphocyanio acid is<br />

sulplwcarhimich (CS N j TT .<br />

AMIDES OF CYANOGEN.<br />

csn<br />

Cyanamidc H > N.—On passing gaseons cyanic acid into a solu-<br />

H I<br />

tion <strong>of</strong> ammonia in e<strong>the</strong>r, ammonium chloride separates out, and <strong>the</strong><br />

solution yields oa evaporation cyanamidc in colourless crystals, which<br />

melt at 40° and are readily soluble in water. On adding nitric acid<br />

to its aqueous solution it is converted into carbamide:—

Hooray! Your file is uploaded and ready to be published.

Saved successfully!

Ooh no, something went wrong!