A = k/e^(-Ea/RT) = (2 × 10⁻⁵)/e^(-80000/2.478) ≈ 5.6 × 10¹³ s⁻¹
Overall order = sum of exponents in rate law = 1 + 2 = 3 (third order reaction)
The rate-determining step (slowest step) controls the overall reaction rate, regardless of how many fast equilibrium steps precede it
For first-order reaction, [A]ₜ = [A]₀(1/2)^(t/t₁/₂). For [A]ₜ = 1/4[A]₀, we need (1/2)^(t/30) = 1/4, so t/30 = 2, giving t = 60 minutes
For zero-order reaction: [A]₀ - [A]ₜ = kt. So 0.5 - 0.1 = 0.02 × t, giving t = 20 s
Using ln(k₂/k₁) = (Ea/R)(1/T₁ - 1/T₂): ln(5.0/1.7) = (Ea/8.314)(1/320 - 1/330), solving gives Ea ≈ 50 kJ/mol
The exponent of [NO] in the rate law is 2, making the reaction second order with respect to NO
Using Arrhenius equation: log(k₂/k₁) = (Ea/2.303R)(T₂-T₁)/(T₁T₂). With Ea = 50,000 J/mol, ΔT = 10 K, this gives log(k₂/k₁) ≈ 0.30, so k₂/k₁ ≈ 2.0
A homogeneous catalyst is in the same phase as reactants. H₂SO₄ (liquid) catalyzes esterification of reactants (liquid), making it homogeneous. Others are heterogeneous catalysts.
When [B]₀ >> [A]₀, the concentration of B doesn't change significantly during the reaction, so it can be incorporated into the rate constant, making the reaction appear first-order in A only.