Friday, January 13, 2017

coordination compounds - How does the addition of acetone cause a shift from hexaaquacobalt(II) to tetrachloridocobaltate(II)?


For this reaction, at equilibrium,


$\ce{[Co(H_2O)_6]^2+ + 4Cl^- <=> [CoCl_4]^2- + 6H_2O}$


$\ce{[Co(H_2O)_6]^2+}$ and $\ce{[CoCl_4]^2-}$ are red and blue in aqueous solution, respectively.


When acetone is then added, the solution changes from red to blue. What causes this?



Answer



I haven't tried this before but it sounds interesting. As the blue chloro-complex is in an equilibrium with the red aqua-complex, I'd suggest the equilibrium is shifted as the water is absorbed by the acetone. As water and acetone are miscible this may take some water from the equilibrium, causing the shift towards the chloro side.


If you use ethanol to dissolve the anhydrous $\ce{CoCl2}$ it will turn blue as well. Yutaka Fukuda mentioned a chloro-ethanol-complex in his book 'Inorganic Chromotropism' for acetone I doubt it will coordinate.


Therefore I'd rather tend to the first one.


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