Step 1: Write the given mechanism.
The overall reaction is:
\[
\text{A}_2 + \text{B}_2 \rightarrow 2\text{AB}
\]
The given mechanism is:
1. \( \text{A}_2 \xrightarrow{k_1} 2\text{A} \) (fast)
2. \( \text{A} + \text{B}_2 \xrightarrow{k_2} \text{AB} + \text{B} \) (slow, rate-determining step)
3. \( \text{A} + \text{B} \xrightarrow{k_3} \text{AB} \) (fast)
Step 2: Identify the rate-determining step (RDS).
The second step is the slow step, so the rate law is determined by this step:
\[
\text{Rate} = k_2[\text{A}][\text{B}_2]
\]
However, [A] is an intermediate, so we need to express it in terms of the stable species (\( \text{A}_2 \) and \( \text{B}_2 \)).
Step 3: Apply the steady-state approximation for [A].
For intermediate A, the rate of formation = rate of consumption.
\[
\text{Rate of formation of A} = \text{Rate of consumption of A}
\]
From step 1 (formation): \( \text{Rate} = 2k_1[\text{A}_2] \)
From steps 2 and 3 (consumption): \( \text{Rate} = k_2[\text{A}][\text{B}_2] + k_3[\text{A}][\text{B}] \)
Equating both rates:
\[
2k_1[\text{A}_2] = k_2[\text{A}][\text{B}_2] + k_3[\text{A}][\text{B}]
\]
\[
[\text{A}] = \frac{2k_1[\text{A}_2]}{k_2[\text{B}_2] + k_3[\text{B}]}
\]
Step 4: Express [B] in terms of [B₂].
In the slow step, B is formed, and from step 3 (fast equilibrium), we can assume:
\[
[\text{B}] \propto [\text{B}_2]^{1/2}
\]
Hence, approximately:
\[
[\text{B}] = k'[\text{B}_2]^{1/2}
\]
Step 5: Substitute and simplify the rate law.
Rate law from step 2:
\[
\text{Rate} = k_2[\text{A}][\text{B}_2]
\]
Substitute [A]:
\[
\text{Rate} = k_2 \left( \frac{2k_1[\text{A}_2]}{k_2[\text{B}_2] + k_3[\text{B}]} \right)[\text{B}_2]
\]
Since [B] ∝ [B₂]¹ᐟ², this implies that the effective dependence on [B₂] will be \( [\text{B}_2]^{1/2} \).
Therefore, the overall rate law is approximately:
\[
\text{Rate} \propto [\text{A}_2]^1 [\text{B}_2]^{1/2}
\]
Hence, the overall order of reaction = 1 + ½ = 1.5.
Final Answer:
\[
\boxed{\text{Overall order of the reaction} = 1.5}
\]