390 THE TRANSITION ELEMENTS
The oxide MnO is obtained by heating the carbonate MnCO 3.
Oxidation of manganese(II) in aqueous acid solution requires a
strong oxidising agent, for example
MnO; (aq) + 8H 3 O+ + 5e' -* Mn^2 +(aq) + 12H 2 O : £e = 1.52 V
MnO 2 (s) + 4H 3 O+ +2e~ ^Mn2+(aq)-h6H 2 O: £^+ 1.35 V
Thus, for example, peroxodisulphate(VI) will oxidise Mn(II) to
Mn(VII):
2Mn2+ + 5SO- + 8HO -» 2MnO + 4 16H+ 4-
However, the Mn(II) ion forms a variety of complexes in solution,
some of which may be more easily oxidised ; these complexes can
be either tetrahedral, for example [MnCl 4 ]^2 ", or octahedral, for
example [Mn(CN) 6 ]^4 '. Addition of ammonia to an aqueous solu-
tion of a manganese(II) salt precipitates Mn(OH) 2 ; reaction of
ammonia with anhydrous manganese(II) salts can yield the ion
[Mn(NH 3 ) 6 ]^2 +.
Low oxidation states
Manganese forms a decacarbonyl Mn 2 (CO) 10 in which each man-
ganese has the required share in 18 electrons to achieve the noble gas
configuration. Reduction of this covalent compound with sodium
amalgam gives the salt Na[Mn(CO) 5 ], sodium pentacarbonyl-
manganate ( - 1); in the ion Mn(CO)^ the noble gas structure is
again attained.
TESTS FOR MANGANESE
Fusion of a manganese compound with sodium carbonate and
potassium nitrate (on porcelain) gives a green manganate(YI) (p. 386).
TEST FOR MnO 4 ION
The purple colour of this ion alone is a sufficient test for its presence:
addition of sulphuric acid and hydrogen peroxide discharges the
colour.
TEST FOR Mn2+ IONS
If a manganese(II) salt is boiled with a strong oxidising agent such