so, let me give you a brief introduction into selected aspects of Co - ions chemistry ...
Co ions will show up in two different "prominent" oxidation states (+ II , + III) , where the respective stability highly depends on the nature of the ligand system accompanying the ion.
this includes a powerfull desire to change oxidation states, shouldn't the ligands at hand be "just right":
(a) Co
2+ in presence of NH
3 badly wants to become oxidized, and turn [Co(NH
3)
6]
3+4 CoCl
2 + 4 NH
4Cl + 20 NH
3 --( oxygen, cat. carbon)--> 4 [Co(NH
3)
6]Cl
3 + 2 H
2O
(b) Co
2(SO
4)
3 in presence of water however will aggressively seek to become + 2 again, and even is powerfull enough in this desire to destroy water oxidatively:
2 Co
2(SO
4)
3 + 2 H
2O --(water)--> 4 Co
2+(aq.) (plus other complexes including sulfate: this depends on conc.) + 4 H
+ + O
2 + 6 SO
42-as a
rule of thumb, aminoligands and thatlike will stabilize the ox. state of +III ( but you'll have to learn those, as there's really no clear system ) , whereas "weak" ligands like water , chloride, nitrate, sulfate will stabilize the (+II) oxidation state
so, first thing to check whenever judging possible reactions of cobalt-ions is, whether they might want to change oxidation state due to the environment you'll expose them to.
fortunately, with the problems given, this is not the case ( as all ligands are stabilizers of ox. state +II , and that's the one we're starting with anyway in Co(NO
3)
2)
so, we'll have to consider none redox reaction whatsoever
however, cobalt being a block II element, its ions are suspects for complex formation (this is a second option of what might happen, even with no redox processes involved)
... and in fact that's what we're about to observe here
In particular, the problem given to you seems to me to be meant to teach you which ligands here are "stronger" (and hence will form, replacing other ligands should the occasion arise), and which are not
so , pls. let's take a look at a 0.1 M solution of Co(NO
3)
2 in water first:
Co((NO
3)
2 + 6 H
2O --(water)--> [Co(H
2O)
6]
2+(aq.) + NO
3-(aq.)so, under these conditions ( i.e. approx c(H
2O) = 55.5 mol/L , c(NO
3-)=0.1 mol/L), nitrate is not strong enough to force the replacement of water in the octahedral coordination sphere of the Co
2+ ion
as , however, this occupation with ligands for a given cation is subject to (sometimes a multitude of) equilibrium reactions, for example
[Me(L
1)
x]
n+ + y L
2 [Me(L
1)
(x-z)(L
2)
z]
n+ + (y-z) L
2 + z L
1we might wish to test for higher conc. of nitrate, and whether those might shift the [Co(H
2O)
6]
2+ situation to something like a [Co(H2O)
5(NO
3)]
+ situation
the result however will be, that nothing happens : nitrate is unable to replace water as a ligand at a Co
2+ , even at high nitrate concentrations:
[Co(H
2O)
6]
2+ + HNO
3 no reaction
with chloride, however, the situation is quite different
[Co(H
2O)
6]
2+ , Cl
- (excess)
[Co(Cl)
4]
2- , water
this change is accompanied by a significant colour change "pale pink / deep blue"
(pls. also note, that along the way cobalt (II) did change the number (and geometry) of coordinated ligands from 6 , octahedral to 4 , tetrahedral )
..and I leave the formulation of a correct, balanced equation to you
for sulfate, there is a similar process, but you will need high conc. of sulfate to really achieve something here, as the complex forming constant isn't that strong:
[Co(H
2O)
6]
2+ , SO
42- (huge excess)
[Co(SO
4)
2]
2-( I couldn't find that much more information with respect to this complex in a hurry, except that it forms with a K-value of approx 2.5
So, if your "chemical heart" is yelling for more information, whether it's of tetrahedral geometry or other, what the colour might be and whether there'd be two more waterligands still present and so on and so forth, you'd have to do some more research on this on your own)
again, I'll leave the formulation of a correct, balanced equation to you
hope this helps a bit
regards
Ingo