Step 1: Understanding the Concept:
For a reaction \(aA \to bB + cC\), the rate of reaction is \(-\frac{1}{a}\frac{d[A]}{dt} = \frac{1}{b}\frac{d[B]}{dt} = \frac{1}{c}\frac{d[C]}{dt}\).
Step 2: Setting up:
For \(2\text{N}_2\text{O}_5 \to 4\text{NO}_2 + \text{O}_2\):
\[ -\frac{1}{2}\frac{d[\text{N}_2\text{O}_5]}{dt} = \frac{1}{4}\frac{d[\text{NO}_2]}{dt} = \frac{d[\text{O}_2]}{dt} \]
Step 3: Detailed Explanation:
\(\text{N}_2\text{O}_5\) disappears at 0.06 mol dm\(^{-3}\) s\(^{-1}\), so
\[ \frac{d[\text{O}_2]}{dt} = \frac{1}{2} \times 0.06 = 0.03 \text{ mol dm}^{-3}\text{s}^{-1} \]
Step 4: Why the other options are wrong.
0.06 (D) would hold only if the coefficients of \(\text{N}_2\text{O}_5\) and \(\text{O}_2\) were equal. 0.02 and 0.04 do not match the 2:1 ratio of \(\text{N}_2\text{O}_5\) used to \(\text{O}_2\) formed.
Final Answer:
Rate of formation of \(\text{O}_2\) is \(0.03\) mol dm\(^{-3}\) s\(^{-1}\), option (B).
\[ \boxed{0.03 \text{ mol dm}^{-3}\text{s}^{-1}} \]