Reaction Rate
Change in concentration per unit time: Rate = -d[A]/dt.
Example: If [N2O5] drops 0.160 to 0.140 M in 200 s, rate = 1.0e-4 M/s.

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Session Length
~17 min
Adaptive Checks
15 questions
Transfer Probes
8
Chemical kinetics studies the rates of chemical reactions, factors influencing rates, and step-by-step mechanisms. The rate law relates reaction rate to reactant concentrations raised to experimentally determined powers. The Arrhenius equation connects rate constants to temperature and activation energy. Reaction mechanisms consist of elementary steps with the rate-determining step governing overall kinetics. Catalysts accelerate reactions by lowering activation energy.
This topic covers rate laws, integrated rate expressions, half-life calculations, the Arrhenius equation, collision theory, transition state theory, reaction mechanisms, intermediates, and catalysis for AP Chemistry Unit 5.
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Change in concentration per unit time: Rate = -d[A]/dt.
Example: If [N2O5] drops 0.160 to 0.140 M in 200 s, rate = 1.0e-4 M/s.
Rate = k[A]^m[B]^n where exponents are experimental orders.
Example: 2NO+O2->2NO2: Rate=k[NO]^2[O2], third order overall.
Minimum energy (Ea) for reaction; barrier to transition state.

Example: H2O2 decomposition: Ea ~75 kJ/mol uncatalyzed, ~8 with catalase.
k=Ae^(-Ea/RT) relates rate constant to T and Ea.
Example: ln k vs 1/T plot gives slope=-Ea/R.
Sequence of elementary steps; must match observed rate law.
Example: Slow step determines Rate=k[NO2][F2].
Lowers Ea via alternative pathway; not consumed; no equilibrium change.
Example: Pt/Pd in catalytic converters lower Ea for exhaust cleanup.
Time for [reactant] to halve. First-order: t1/2=0.693/k.
Example: C-14 half-life=5730 years regardless of starting amount.
Reactions need collisions with energy >= Ea and proper orientation.
Example: Only properly oriented NO+O3 collisions with enough energy react.
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