Understanding reaction rates is key in chemistry. Kinetics formulas help us analyze how reactant concentrations and temperature affect the speed of reactions, guiding us through concepts like rate laws, half-lives, and the impact of catalysts on reaction pathways.
-
Rate law equation: rate = k[A]^m[B]^n
- The rate of a reaction depends on the concentration of reactants raised to a power.
- The exponents (m and n) indicate the order of the reaction with respect to each reactant.
- The rate constant (k) is specific to the reaction and varies with temperature.
-
Integrated rate law for zero-order reactions: [A] = -kt + [A]₀
- The concentration of reactant decreases linearly over time.
- The rate is constant and does not depend on the concentration of reactants.
- The half-life is directly proportional to the initial concentration.
-
Integrated rate law for first-order reactions: ln[A] = -kt + ln[A]₀
- The concentration of reactant decreases exponentially over time.
- The rate depends linearly on the concentration of the reactant.
- The half-life is constant and independent of the initial concentration.
-
Integrated rate law for second-order reactions: 1/[A] = kt + 1/[A]₀
- The concentration of reactant decreases in a non-linear fashion over time.
- The rate depends on the square of the concentration of the reactant.
- The half-life is inversely proportional to the initial concentration.
-
Half-life formula for first-order reactions: t₁/₂ = ln(2)/k
- The half-life is a constant value for first-order reactions.
- It indicates the time required for half of the reactant to be consumed.
- The value of k directly affects the duration of the half-life.
-
Arrhenius equation: k = Ae^(-Ea/RT)
- The rate constant (k) increases with temperature and decreases with activation energy (Ea).
- A is the pre-exponential factor, representing the frequency of collisions.
- R is the universal gas constant, and T is the temperature in Kelvin.
-
Collision theory equation: k = pZe^(-Ea/RT)
- The rate constant (k) is influenced by the frequency of effective collisions (p) and the orientation of molecules (Z).
- Activation energy (Ea) must be overcome for a reaction to occur.
- Higher temperatures increase the number of effective collisions.
-
Catalyst effect on activation energy: Ea(catalyst) < Ea(uncatalyzed)
- Catalysts lower the activation energy, increasing the reaction rate.
- They provide an alternative pathway for the reaction.
- Catalysts are not consumed in the reaction and can be reused.
-
Relationship between rate constant and temperature: ln(k₂/k₁) = (Ea/R)(1/T₁ - 1/T₂)
- This equation shows how the rate constant changes with temperature.
- It allows for the comparison of rate constants at two different temperatures.
- A higher temperature generally results in a higher rate constant.
-
Rate determining step in a multi-step reaction: overall rate = rate of slowest step
- The slowest step in a reaction mechanism controls the overall reaction rate.
- Identifying the rate-determining step is crucial for understanding reaction kinetics.
- The rate law can often be derived from the rate-determining step.