Uploaded November 2017 | Updated September 2026, 1 week ago
If you have seen our video on the equilibrium between [Co(H2O)6](2+) and [CoCl4](2-) you probably thought this could be possible with similar compounds as well.
So what we did here was to mix CuCl2 with H2O and HCl to a ratio where the nearly colorless, blue [Cu(H2O)6](2+) is turned into the green [CuCl4](2-) when it is heated.
If you have seen our video on the equilibrium between [Co(H2O)6](2+) and [CoCl4](2-) you probably thought this could be possible with similar compounds as well.
So what we did here was to mix CuCl2 with H2O and HCl to a ratio where the nearly colorless, blue [Cu(H2O)6](2+) is turned into the green [CuCl4](2-) when it is heated.

. So why is it stable in aqueous conditions ?
Lets assume we had Copper(I) in a gas phase, free from any solvation- or hydration energy. To make Cu(II) we require a lot of Ionizationenergy. This makes the reaction really endothermic. If we take it and dissolve it into Acetonitrile, lets say CuCl which is soluble in Acetonitrile, it will dissolve and stay as Cu(I). The reason for this is that the solvationenergy in Acetonitrile is too low to overcome this ionization energy. Water however produces a quite large Energy and Cu(II) can be formed under disproportionation.
Now what happens in this experiment ?
2 Cu(I) to Cu(II) and Cu(0) is an equilibrium. In water it is exothermic forming Cu(II). And if you work with Cu(II) solutions it wont turn into Cu(I) (unless you add an reducing agent like Sulfite) as no Cu(0) is present to shift the equilibrium back. As we know from Le Chatelier, if a reaction is exothermic, heat causes the system to go back to the endothermic side. So Cu(I) forms and combines with the Cl(-) which is present to form CuCl. CuCl is insoluble in water as the lattice energy is higher than the hydration energy and thus Cu(I) remains stable discoloring the blue solution over time. Copper Chemistry: Synproportionation Cu(II) and Cu(0)](https://i.ytimg.com/vi/mGx4hOx7YdY/mqdefault.jpg)








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If Co(II) solutions are treated with alkaline H2O2 Co2O3 and CoO2 may form. If however the precipitate from Sodium Bicarbonate and Cobalt Chloride is oxidized with a 10 M H2O2 at cold temperatures a green product froms.
Well we used worm solutions, 3% Hydrogen Peroxide and Sodium Carbonate but still got a green compound. Of course we cant be sure about its composition that way. It could also be the different oxides but the green color at least indicates some of the complex might have actually formed that way.
The Co(II) is oxidized to Co(III) which forms an insoluble complex with Na2CO3, Na3[Co(CO3)3]. Interesting enough the carbonate can be easily substituted for other ligands making this complex a great precursor to other Co(III) compounds.
We already discussed the chemistry of Co(II) and Co(III) in another video and showed that the oxidation potential is highly dependend on the system you use Cobalt in. Cobalt Chemistry: [Co(CO3)3](3-) (???) [no audio]](https://i.ytimg.com/vi/p8TuAZuQeTU/mqdefault.jpg)