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A Manual of the Chemistry of the Carbon Compounds

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THE CARBON COMPOUNDS. 55<br />

mixing <strong>the</strong> alcoholic solution with e<strong>the</strong>r, <strong>the</strong> compound is precipitated<br />

as a crystalline powder. When exposed to <strong>the</strong> air, it absorbs<br />

oxygen; prussic acid is given <strong>of</strong>f, and prhssian blue formed; this<br />

change takes place more quickly on <strong>the</strong> application <strong>of</strong> heat Hydrir<br />

ferrocyanide is a strong acid which decomposes not only carbonates<br />

but also acetates and oxaktes. On boiling its aqueous solution hydro<br />

cyanic acid is given <strong>of</strong>f and a white precipitate <strong>of</strong> ferrous ferrocyanidi 1<br />

FeaCfy = Fe3(CN)fl is formed :—<br />

3H4(CN)0 « 12HCN + Fe8(CNj6<br />

This decomposition occurs in <strong>the</strong> preparation <strong>of</strong> prussic acid from<br />

potassium ferrocyanide and dilnte sulphuric acid.<br />

The ferrocyamdes <strong>of</strong> o<strong>the</strong>r metals are ei<strong>the</strong>r sparingly soluble in<br />

water or insoluble, and are <strong>the</strong>refore obtained as precipitates by adding<br />

a solution <strong>of</strong> potassium ferrocyanide to solutions <strong>of</strong> metallic salts;<br />

potassium ferrocyanide is for this reason used as a reagent-. Tints<br />

with solutions <strong>of</strong> barium salts it gives a crystalline precipitate having<br />

<strong>the</strong> composition BaK2Cfy, and by adding a solution <strong>of</strong> <strong>the</strong> ferrocyaoide<br />

to a solution <strong>of</strong> copper sulphate, a red precipitate <strong>of</strong> copper<br />

ferrocyanide Cu1|SOfy 19 formed; whilst by adding a solution <strong>of</strong> a<br />

cupric salt to, an excess <strong>of</strong> potassium ferrocyanide a brown precipitate<br />

CuKaCfy is obtained.<br />

Potassium Ferricyanidc K3Cfdy.—This compound, commonly<br />

known as red prussiate <strong>of</strong> potash, is prepared by passing chlorine int©<br />

a solution <strong>of</strong> potassium ferrocynnide:—<br />

K4(CN)8Fe + Cl = KC1 + K3(CN)4Fo<br />

Potassium chloride and ferricyauide are formed and separated fromone<br />

ano<strong>the</strong>r by crystallization. The red prussiate crystallizes in large,<br />

dark red, mouoclinic prisms, solnble in water with a brownish green<br />

colour. By reducing agents it is re-converted into a ferrocyanide;<br />

this is easily effected by adding potassium amalgam to its aqueous<br />

solution. Its alkaline solution is, <strong>the</strong>refore, a powerful oxidizing<br />

agent; it converts chromic oxide into chromic acid, and manganese<br />

monoxide into <strong>the</strong> dioxide:—<br />

6TCg(CN)0Fe + 10HOK + Cr8O3 = 6K4(CN)6Fe + 2K2Cr0, +• 5HjO<br />

Ferric salts are not precipitated by <strong>the</strong> addition <strong>of</strong> potassium ferrieyauide,<br />

<strong>the</strong> solution only assumes a dark brown colour ; but with<br />

ferrons salts it produces a dark bhte precipitate, called Turnlults<br />

bhte, which is generally considered to consist <strong>of</strong> ferrous ferricijanidi<br />

Fes(Cfdy)2. This precipitate, however, has <strong>the</strong> same composition.<br />

and <strong>the</strong> same properties as <strong>the</strong> compound %|N [ Cfya, \vhich, aa we-<br />

have seen, forms <strong>the</strong> chief constituent <strong>of</strong> prussiatt blue, and it appears<br />

highly probable that <strong>the</strong> two compounds are identical. Its formation<br />

is easily explained. By bringing toge<strong>the</strong>r ferricyanide <strong>of</strong> potassium<br />

and a ferrous salt, a part <strong>of</strong> <strong>the</strong> latter is oxidized, a ferric salt being

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