IndietroChemical Kinetics and Chemical Equilibrium: Study Guide Notes
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Chemical Kinetics
Factors Affecting Reaction Rates
Chemical kinetics studies the speed at which chemical reactions occur and the factors that influence these rates.
Temperature: Increasing temperature generally increases reaction rate by providing more energy for collisions.
Concentration: Higher concentration of reactants leads to more frequent collisions, increasing the rate.
Surface Area: For reactions involving solids, increasing surface area (e.g., by grinding) exposes more particles to react, increasing rate.
Catalyst: Catalysts lower the activation energy, increasing the rate without being consumed.
Example: A reaction proceeds faster at 50°C than at 25°C due to increased molecular motion.
Expressing and Calculating Reaction Rates
The rate of a reaction is the change in concentration of a reactant or product per unit time.
Average Rate: , where is concentration and is time.
Instantaneous Rate: The rate at a specific moment, found by the slope of the concentration vs. time curve.
Example: If decreases from 0.10 M to 0.08 M in 20 seconds, M/s.
Rate Laws and Determining Reaction Order
A rate law expresses the relationship between the rate and the concentration of reactants.
General Form:
Order of Reaction: The exponents and indicate the order with respect to each reactant; the sum is the overall order.
Determining Order: Use experimental data to see how rate changes with concentration.
Example: If doubling doubles the rate, the reaction is first order in .
Integrated Rate Laws and Calculations
Integrated rate laws relate concentrations of reactants to time for different reaction orders.
Zero Order:
First Order:
Second Order:
Half-life ():
First Order:
Second Order:
Zero Order:
Example: For a first-order reaction with s, s.
Reaction Mechanisms and Rate Laws
A reaction mechanism is a sequence of elementary steps that describes how a reaction occurs at the molecular level.
Elementary Step: A single step in a mechanism, with its own rate law.
Rate-Determining Step: The slowest step, which controls the overall rate.
Writing Rate Laws from Mechanisms: The rate law is based on the rate-determining step, using only reactants involved in that step.
Example: If the slow step is , then .
Chemical Equilibrium
Equilibrium Expressions
Chemical equilibrium occurs when the rates of the forward and reverse reactions are equal, and concentrations remain constant.
Equilibrium Constant (): for the reaction .
Only gases and aqueous species appear in ; solids and pure liquids are omitted.
Example: For , .
Calculations Involving Equilibrium (ICE Tables)
ICE (Initial-Change-Equilibrium) tables help organize data for equilibrium calculations.
Initial: Starting concentrations
Change: Amounts that react or form (use variables like or )
Equilibrium: Final concentrations, used in the equilibrium expression
Example: If M, M, and mol/L of reacts, then at equilibrium , .
Reaction Quotient () and Direction of Reaction
The reaction quotient is calculated like but with current (not necessarily equilibrium) concentrations.
If : Reaction proceeds forward (toward products).
If : Reaction proceeds in reverse (toward reactants).
If : System is at equilibrium.
Example: If and , the reaction will shift right to reach equilibrium.
Le Chatelier’s Principle
Le Chatelier’s Principle states that if a system at equilibrium is disturbed, it will shift to counteract the disturbance.
Concentration: Adding reactant shifts equilibrium toward products; removing reactant shifts toward reactants.
Pressure/Volume (for gases): Increasing pressure (decreasing volume) shifts equilibrium toward the side with fewer moles of gas.
Temperature: Increasing temperature favors the endothermic direction; decreasing favors exothermic.
Example: For an exothermic reaction, increasing temperature shifts equilibrium toward reactants.
Common Equations Provided
Equation | Description |
|---|---|
First-order integrated rate law | |
Zero-order integrated rate law | |
Second-order integrated rate law | |
First-order half-life | |
Second-order half-life | |
Zero-order half-life | |
Quadratic formula (used in equilibrium calculations) |