SECTION 5 - KINETICS Flashcards
Thermodynamics
Tells us how much of a reaction will take place
Kinetics
Tells us how fast a reaction will happen
3 main things that influence reaction rate
- Temperature (higher –> faster)
- Surface area (larger –> faster)
- Concentration (higher –> faster)
Triangle
Change in
Reaction rate
Quantitative measure of how fast the reaction proceeds to consume the reactants/produce the products
+ sign
Product (appearance)
- sign
Reactants (dissapearence)
Differential rate law
Equations that tell us how the instaneous rate changes with reactant concentrations
Rate law
K[A]^n relationship between concentration and rate
Zero order
Rate is NOT dependant on concentration of reactants k[A]^0 (constant)
First order
Rate is dependant on concentration of reactants k[A]^1 (2x)
Second order
Rate is dependant on concentration of reactants k[A]^2 (4x)
Units of k
- Zero order: M L s-1
- First order: s-1
- Second order: L M -1 s -1
Multiple reactant reaction
The overall order becomes the sum of the reactant exponents
Integrated rate law
Relationship between concentration and time
What do we do with minutes in integrated rate law
Convert to seconds
Half life (t1/2)
The time it takes for one half of a given amount of reactant to be consumed (time used to use half of reactant)
Collision theory
Tells us that the reactant particles (ion/atom/molecule) must collide in order to reactant (higher reactant concentration = higher probability of success)
Postulates of collision theory
- Reaction rate is proportional to the number of reactant collisions
- Reactants must be properly oriented when they collide for reaction to occur
- Reactants must have kinetic energy when colliding
Activation energy
Minimum amount of energy needed for molecules to collide for reaction to occur
Vertical axis of activation energy diagram
Potential energy (P.E), enthalpy (H), Gibbs energy (G)
Horizontal axis of activation energy diagram
Time
-H
Exothermic (release heat)
+H
Endothermic (absorb heat)
Transition state
Top of the energy curve
Arrhenius equation
Relates raw and temperature k=Ae^ -Ea/RT
A
Frequency factor (how often correct collisions occur)
e^
exponential factor (describes temperature effect on K)
R
Universal gas constant 8.314 J K-1 mol-1
T
Temperature in Kelvins
Ea
Activation energy
If Ea increases
e^-x decrease, k decrease, rate decrease
If Ea decreases
e^-x increase, k increase, rate increase
If K increase
e^smaller number, k increase, T increase, k increase
Reaction mechanism
Series of steps by which an overall chemical reaction occurs
Elementary steps
Term for the individual steps in reaction mechanism
Catalysts
Increase rate of reaction by decreasing activation energy
Homogenous catalysts
Same phase/state as reactants
Heterogenous catalysts
Different phase/state as reactants
Enzymes
Catalysts in biological systems
Substrate
Active sites on enzymes that hold reactants substrate
Maud Menten & Leonor Michaels
First described single substrate enzyme reactions