Online Encyclopedia

CYANIC ACID AND CYANATES

Online Encyclopedia
Originally appearing in Volume V07, Page 680 of the 1911 Encyclopedia Britannica.
Spread the word: del.icio.us del.icio.us it!

CYANIC

ACID AND CYANATES  . Cyanic acid, CN•OH, was discovered by F . Wohler in 1824, and may be obtained by distilling its polymeride, cyanuric acid, in a current of carbon dioxide (F . Wohler and J. v . Liebig, Berzelius Jahresberichte, 1827, 11, p . 84), the vapours which distil over being condensed in a freezing mixture . It is a very volatile liquid of strong acid reaction, and is only
See also:
stable below o° C . It has a smell resembling that of acetic acid . At o° C. it is rapidly converted into a mixture of cyanuric acid, C3N3O3H3, and another polymer, cyamelide (CNOH)x; this latter substance is a white amorphous powder, insoluble in
See also:
water . An aqueous solution of cyanic acid is rapidly hydrolysed (above (a° C.) into a mixture of carbon dioxide and
See also:
ammonia . Cyanogen chloride, CNC1, may be regarded as the chloride of cyanic acid . It may be prepared by the
See also:
action of chlorine on hydrocyanic acid or on mercury
See also:
cyanide .

It is a very poisonous volatile liquid, which boils at 15.5° C . It polymerizes readily to cyanuric chloride, C3N3C13 .

Caustic alkalis hydrolyse it readily to the alkaline chloride and cyanate . The salts of cyanic acid are known as the cyanates, the two most important being potassium cyanate (KOCN) and ammonium cyanate (NH4OCN) . Potassium cyanate may be prepared by
See also:
heating potassium cyanide with an oxidizing agent, or by heating potassium ferrocyanide with manganese dioxide, potassium carbonate or potassium dichromate (J. v . Liebig,
See also:
Ann., 1841, 38, p . 108; C . Lea, Jahresb., 1861, p . 789; L . Gattermann, Ber., 1890, 23, p . 1224), the fused mass being extracted with boiling
See also:
alcohol . It crystallizes in flat plates and is readily soluble in cold water .

It is a somewhat important reagent, and has been used by Emil

Fischer in various syntheses in the uric acid
See also:
group (see
See also:
PuRIN) . Ammonium cyanate possesses considerable theoretical importance since the first synthetical production of an organic from inorganic compounds was accomplished by warming its aqueous solution for some time, urea being formed (F . Wohler, Berzelius Jahresberichte, 1828, 12, p . 266) . J . Walker and J . K . Wood (Jour . Chem .
See also:
Soc., 1900, 77, p . 24) prepared pure ammonium cyanate by the union of gaseous ammonia and cyanic acid,
See also:
special precautions being taken to keep the temperature below the point at which the salt is trans-formed into urea . It crystallizes in
See also:
fine needles, which melt suddenly at about 8o° C., then resolidify, and melt again at about 128° to 130° C .

(this temperature being that of the melting point of urea) . Substituted ammonias were also made to combine with cyanic acid, and it was found that the substituted ammonium cyanates produced pass much more readily into the corresponding ureas than ammonium cyanate itself . (On the constitution of cyanic acid see F . D . Chattaway and J . M . Wadmore, Jour . Chem . Soc., 1902, 81, p . 191.)

See also:
Esters of normal cyanic acid are not known, but those of isocyanic acid (HN•CO) may be prepared by the action of alkyl halides on
See also:
silver cyanate, or by oxidizing the isonitriles with mercuric
See also:
oxide . They are volatile liquids which
See also:
boil without decomposition, and possess a nauseating smell . When hydrolysed with caustic alkalis, they yield
See also:
primary
See also:
amines (this reaction determines their constitution) .

C2H5NCO +

H2O= C2H5NH2 +
See also:
CO2 . When heated with water they yield carbon dioxide and symmetrical dialkyl ureas; with ammonia and amines they form alkyl ureas; and with acid anhydrides they yield
See also:
tertiary amides .
See also:
Ethyl isocyanate, C2H5NCO, was first prepared by A . Wurtz ( Ann.chim., 1854 (3), 42, p . 43) by distilling a mixture of potassium ethyl sulphate.and potassium cyanate . It is a colourless liquid which boils at 6o C . Cyanuric acid, H3C3N303, was obtained by Wohler and Liebig by heating urea, and by A . Wurtz by passing chlorine into melting urea . It forms white efflorescent crystals . Treatment with phosphorus pentachloride gives cyanuric chloride, C3N3C13, which is also formed by the combination of anhydrous chlorine and prussic acid in the presence of sunlight . These substances contain a ring of three carbon and three nitrogen atoms, i.e. they are symmetrical triazines .

End of Article: CYANIC ACID AND CYANATES
[back]
CYANAMIDE
[next]
CYANIDE

Additional information and Comments

There are no comments yet for this article.
» Add information or comments to this article.
Please link directly to this article:
Highlight the code below, right click and select "copy." Paste it into a website, email, or other HTML document.