Chapter 5- Chemical Kinetics Flashcards
Collision theory of chemical kinetics and reaction rate
Rate of a reaction is proportional to the number of collisions per second between the reacting molecules
Rate= Zf Z = total number of collisions per second f = fraction of collisions that are effective
Arrhenius equation about collision of molecules
Rate= Ae^(-Ea/RT) A= frequency factor R= ideal gas constant T= temp in kelvin
+ Gibbs free energy
Endergonic, energy absorbed, nonspontaneous
- Gibbs free energy
Exergonic, energy given off, spontaneous
Temp for enzymes in human body
Between 35 and 40 Celsius (body temp)
Rate law
Rate = k[A]^x[B]^y
Only reactants and k, x, and y must be found experimentally for a certain reaction at a certain temperature
Zero order reaction
rate of product formation is independent of changes in concentrations
Can change with temp b/c k is dependent on temperature
Linear graph slope, -k
Higher order reactions
Mixed order reactions
Higher- 3rd order rates
Mixed- noninteger orders (fractions). Reaction appears to be first order then when the reactant is low it kicks in and speeds up again
First order reactions
Directly proportional to one reactant
[A]e^-kt
Nonlinear graph
Second order reactions
Proportional to either concentrations of two reactants or to the square of the concentration of a single reactant
Nonlinear curved graph.