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Exercises · 7.20

Q.What sorts of informations can you draw from the following reaction ? (CN)2(g) + 2OH–(aq) → CN–(aq) + CNO–(aq) + H2O(l)

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This reaction shows the disproportionation of cyanogen (CN)2(CN)_2 in a basic medium — it is simultaneously reduced to CN−CN^- and oxidised to CNO−CNO^-. The oxidation number of carbon changes from +3+3 in (CN)2(CN)_2 to +2+2 in CN−CN^- and +4+4 in CNO−CNO^-, confirming a redox reaction where the same species acts as both oxidant and reductant.

Concept First — Why This Reaction is Interesting

At first glance, this looks like a simple neutralisation or substitution. But look closer: the same reactant, (CN)2(CN)_2, gives two different products containing cyanide. That's the hallmark of disproportionation — a reaction where one substance is both oxidised and reduced.

To see this, we track the oxidation numbers of carbon and nitrogen. Cyanogen (CN)2(CN)_2 is like a dimer of cyanide: N≡C−C≡NN \equiv C - C \equiv N. Each carbon is bonded to a nitrogen (more electronegative) and to the other carbon. In CN−CN^-, carbon is bonded only to nitrogen. In CNO−CNO^- (cyanate), carbon is bonded to both nitrogen and oxygen.

The key insight: the same element (carbon) changes oxidation state in opposite directions in the two products. That's the definition of disproportionation.


Step-by-Step Analysis

1. Assign oxidation numbers to carbon in each species

We use standard rules:

  • Oxygen is −2-2 (except in peroxides).
  • Nitrogen is more electronegative than carbon, so in each CC–NN bond nitrogen is assigned its usual value of −3-3 (as in nitriles/cyanides), and the oxidation number of carbon in each species follows from that.
Watch out

A common mistake: assume nitrogen always has −3-3 in cyanides. In CN−CN^-, the sum of oxidation numbers equals the charge −1-1. If N is −3-3, then C must be +2+2 to give −1-1. But in (CN)2(CN)_2, the molecule is neutral, so each CNCN unit must sum to 00. That forces N to be −3-3 and C to be +3+3 in (CN)2(CN)_2. Check: +3+(−3)=0+3 + (-3) = 0.

Let's verify systematically:

  • In (CN)2(CN)_2: molecule is neutral. Each CNCN unit has net charge 00. Let xx = oxidation number of C, yy = oxidation number of N. For one CNCN unit: x+y=0x + y = 0. Since N is more electronegative than C, y=−3y = -3 (usual for N in nitriles). Then x=+3x = +3. So C in (CN)2(CN)_2 is +3+3.

  • In CN−CN^-: ion charge −1-1. So x+y=−1x + y = -1. With y=−3y = -3, we get x=+2x = +2. So C in CN−CN^- is +2+2.

  • In CNO−CNO^- (cyanate ion): structure is [N≡C−O]−[N \equiv C - O]^-. Let xx = oxidation number of C, yy = N, zz = O. Oxygen is −2-2. The sum: x+y+(−2)=−1x + y + (-2) = -1 (charge). So x+y=+1x + y = +1. Nitrogen is more electronegative than C, so y=−3y = -3. Then x=+4x = +4. So C in CNO−CNO^- is +4+4.

Oxidation numbers of carbon:

(CN)2(CN)_2: +3+3

CN−CN^-: +2+2

CNO−CNO^-: +4+4

2. Identify the redox changes

From (CN)2(CN)_2 to CN−CN^-: carbon goes from +3+3 to +2+2 — reduction (gain of electrons).

From (CN)2(CN)_2 to CNO−CNO^-: carbon goes from +3+3 to +4+4 — oxidation (loss of electrons).

So the same reactant is both reduced and oxidised. That's disproportionation (also called dismutation).

3. What about nitrogen?

In all three species, nitrogen stays at −3-3 (check: in CNO−CNO^-, y=−3y = -3 as assumed; in CN−CN^-, y=−3y = -3; in (CN)2(CN)_2, y=−3y = -3). So nitrogen does not change oxidation state. The redox action is entirely on carbon.

4. Balance the half-reactions (optional but instructive)

Reduction half:

(CN)2+2e−→2CN−(CN)_2 + 2e^- \rightarrow 2CN^-

(Each C gains 1 electron, so two C gain 2 electrons.)

Oxidation half:

(CN)2+4OH−→2CNO−+2H2O+2e−(CN)_2 + 4OH^- \rightarrow 2CNO^- + 2H_2O + 2e^-

(Each C loses 1 electron, so two C lose 2 electrons.)

Adding them:

(CN)2+(CN)2+4OH−+2e−→2CN−+2CNO−+2H2O+2e−(CN)_2 + (CN)_2 + 4OH^- + 2e^- \rightarrow 2CN^- + 2CNO^- + 2H_2O + 2e^-

Cancel the 2e−2e^- and combine the two (CN)2(CN)_2:

2(CN)2+4OH−→2CN−+2CNO−+2H2O2(CN)_2 + 4OH^- \rightarrow 2CN^- + 2CNO^- + 2H_2O …

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