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Rodanic acid

Rodovodorodnaya (thiocyanic) acid - a yellowish, oily, sharp-smelling liquid . Chemical formula HNCS [1] .

Rodanic acid
Thiocyanic acid.svg
Rodovodorodnaya acid, Thiocyanic acid.png
Are common
Traditional namesthiocyanic acid, rhodium hydrogen
Chem. formulaHNCS
Physical properties
Molar mass59.0917 g / mol
Thermal properties
T. melt.−110 ° C
T.−90 ° C
Mol heat capacity48.16 J / (mol · K)
Education enthalpy104.6 kJ / mol
Chemical properties
Water solubilitydissolves
Classification
Reg. CAS number463-56-9
Pubchem
Reg. EINECS number
SMILES
Inchi
CHEBI
Chemspider

Content

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Earlier, it was widely believed that thiocyanic acid is a mixture of two tautomers:

H-S-C≡N⇄H-N=C=S{\ displaystyle {\ mathsf {H {-} S {-} C \ equiv N \ rightleftarrows H {-} N {=} C {\ text {=}} S}}}  

but later it turned out that the acid has the structure of HNCS. The alkali metal and ammonium thiocyanates have the formula Me + NCS - , the formula Me (SCN) x is possible for other thiocyanates.

Physical and chemical properties

Hydrogenic acid is stable only at low temperatures (about –90 ° C) or in dilute aqueous solutions (less than 5%). It is a strong acid - its solutions are almost completely dissociated. It is well soluble in water and a number of organic solvents ( ethanol , diethyl ether , benzene ).

In the range from –90 ° C to –85 ° C, it polymerizes to a colorless crystalline mass. With weak heating in vacuum , rhodanuric acid (HNCS) 3 is formed , which passes back to HNCS at 3-5 ° C. Density = 2.04 g / cm 3 .

Aqueous solutions are stable up to 5% concentration, in more concentrated solutions decomposes, turning into so-called. Xanthogen hydrogen and a number of other products.

Reacts with alkali metals . It is reduced by zinc in hydrochloric acid to methylamine and 1,3,5-trithiane ( thioformaldehyde trimer).

tenZn+20HCl+eightHNCS→3(HCSH)3+2CH3NH2+tenZnCl2{\ displaystyle {\ mathsf {10Zn + 20HCl + 8HNCS \ rightarrow 3 (HCSH) _ {3} + 2CH_ {3} NH_ {2} + 10ZnCl_ {2}}}}  

It is oxidized with potassium permanganate to sulfuric acid, hydrogen peroxide to hydrocyanic acid , bromine to bromine cyanide .

2HNCS+2KMnOfour→H2SOfour+2MnO 2 ↓ + 2 K C N O + S ↓{\ displaystyle {\ mathsf {2HNCS + 2KMnO_ {4} \ rightarrow H_ {2} SO_ {4} + 2MnO_ {2} \ downarrow + 2KCNO + S \ downarrow}}}  
2HNCS+2KMnOfour→H2SOfour+2MnO2↓+2KCN+SO2↑{\ displaystyle {\ mathsf {2HNCS + 2KMnO_ {4} \ rightarrow H_ {2} SO_ {4} + 2MnO_ {2} \ downarrow + 2KCN + SO_ {2} \ uparrow}}}  
2HSCN+Br2→2BrCN+H2S2↑{\ displaystyle {\ mathsf {2HSCN + Br_ {2} \ rightarrow 2BrCN + H_ {2} S_ {2} \ uparrow}}}  

Slow oxidation leads to rodan (SCN) 2 . Hydrogen sulfide decomposes to carbon disulfide and ammonia . Attaches to unsaturated compounds. Salts of this acid are called thiocyanates .

H2S+HNCS→CS2↑+NH3↑{\ displaystyle {\ mathsf {H_ {2} S + HNCS \ rightarrow CS_ {2} \ uparrow + NH_ {3} \ uparrow}}}  

The formation of blood-red thiocyanate-ion complexes with the Fe 3+ ion is one of the qualitative reactions to iron.

Application

Practical use is found only for the salts of hydrocyanic acid, as well as its esters , used as insecticides and fungicides .

Notes

  1. ↑ Chemical encyclopedia / Redcol .: Knunyants I.L. et al. - M .: Soviet Encyclopedia, 1995. - Vol. 4 (Paul-Three). - 639 s. - ISBN 5-82270-092-4 .

Literature

  • Chemical Encyclopedia / Redkol .: Knunyants I.L. et al. - M .: Soviet Encyclopedia, 1995. - Vol. 4 (Paul-Three). - 639 s. - ISBN 5-82270-092-4 .
Source - https://ru.wikipedia.org/w/index.php?title= Hydrofluoric acid&oldid = 96795253


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