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Chemistry · Ch 13 — General Principles and Processes of Isolation of Elements

Oxidation Reduction

13.6

Oxidation Reduction

The cyanide leaching of gold and silver introduced in Section 6.2.4 is worth looking at again through a slightly different lens — as a genuine oxidation–reduction pair, not just a solubility trick.

The oxidation step

Leaching gold with cyanide in the presence of air converts the metal itself: Ag→Ag+Ag \rightarrow Ag^+ or Au→Au+Au \rightarrow Au^+. That's an oxidation of the metal, driven by atmospheric O2O_2:

4Au(s)+8CN−(aq)+2H2O(aq)+O2(g)→4[Au(CN)2]−(aq)+4OH−(aq)(6.48)4Au(s) + 8CN^-(aq) + 2H_2O(aq) + O_2(g) \rightarrow 4[Au(CN)_2]^-(aq) + 4OH^-(aq) \qquad(6.48)

The reduction step

The gold is then recovered from solution by a displacement reaction with zinc:

2[Au(CN)2]−(aq)+Zn(s)→2Au(s)+[Zn(CN)4]2−(aq)(6.49)2[Au(CN)_2]^-(aq) + Zn(s) \rightarrow 2Au(s) + [Zn(CN)_4]^{2-}(aq) \qquad(6.49)

Here zinc is the reducing agent — it gives up electrons more readily than gold does, pushing Au+Au^+ back down to metallic Au(s)Au(s) while zinc itself goes into solution as the cyanide complex.

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