GROUP IV 199
Tin(II) chloride is slowly oxidised in air, but keeping a piece of tin
metal in the solution prevents this.
TIN(IV) CHLORIDE, SnCl 4
Stannic chloride is prepared by treating metallic tin with chlorine:
Sn + 2C1 -+ SnCl 4
(This reaction has been used to recover tin from scrap tinplate.)
Tin(IV) chloride is a colourless liquid, which fumes in air due to
hydrolysis:
SnCl 4 + 2H 2 O ^--- SnO 2 + 4HC1
hyd rated
It is soluble in organic solvents (a characteristic of a covalent com-
pound), but dissolves in water and can form hydrates (a character-
istic of an ionic compound). Hence the hydra ted Sn4+ must be
formed in water and undergo hydrolysis thus (cf. aluminium):
Kn[Sn.xH vH OH* 2 O] - Sn _ +°H T+ +H H "- 2)H 2 O
This process goes on until (if alkali is added) the final product is
[Sn(OH) 6 ]^2 ~. (If alkali is not added, hydrolysis ultimately gives the
hydrated oxide in accordance with the equation above.) The
hydrolysis can be suppressed by addition of hydrochloric acid, and
with excess of this, hexachlorostannic(IV) acid is formed:
SnCl 4 4- 2HC1 -> H 2 SnIVCl 6
Salts of this acid are known and ammonium hexachlorostan-
nate(IV) (NH 4 ) 2 SnQ 6 , is used as a mordant.
Lead
LEAD(II) CHLORIDE
The solid is essentially ionic, made up of Pb2+ and Cl~ ions. The
vapour contains bent molecules of PbCl 2 (cf. SnCU). Lead chloride
is precipitated when hydrochloric acid (or a solution of a chloride)
is added to a cold solution of a lead(II) salt. It dissolves in hot water
but on cooling, is slowly precipitated in crystalline form. It dissolves
in excess of concentrated hydrochloric acid to give the acid
H 2 [Pb"Cl 4 ].