Unit I: Thermodynamics, Kinetics Flashcards
1st Law of Thermodynamics
energy can be converted from one form to another but cannot be created or destroyed
Enthalpy
- known as H, units are KJ/mole
- energy in a system plus work on the system or internal energy plus product of pressure and volume
specific heat capacity
- denoted by “c”
- quantity of heat required to change 1 gram of a substance by 1 K (J/g*K)
Equation when given any of following: specific heat capacity, mass, change in temperature, heat.
q = m x c x ΔT
q is heat in joules
m is mass
c is specific heat capacity
T is temperature
Hess’s Law
the enthalpy change of an overall process is the sum of the enthalpy changes of its individual steps
Bond Energy
energy needed to overcome the attraction between two atoms
Bond Order
- # of electron pairs shared by two atoms
- single bond = 1, etc.
Bond Length
distance between nuclei of two bonded atoms
Heat of Vaporization
Δ Hvap - heat required to vaporize something (KJ/mole)
Heat of Fusion
Δ Hfus - heat required to melt something (KJ/mol)
entropy
- randomness, the freedom of motion of particles in a system
- greater freedom = greater # particles = more systemic disorder = greater entropy
2nd Law of Thermodynamics
- entropy of the universe increases _for spontaneous processes _
3rd Law of Thermodynamics
- entropy of a perfect crystalline solid is zero at absolute zero ( 0 K)
- this basically means there is entropy in everything since perfection and absolute zero are non-existent in nature
Gibbs Free Energy Equation
ΔG = ΔH - TΔS
- G is free energy, H is enthalpy, S is entropy, T is temperature
- if ΔG < 0, rxn is spontaneous
- ΔG > 0, rxn is not spontaneous
- ΔG = 0, rxn is in equilibrium
Rate Law
- predicts how fast a reaction will occur given the initial concentration of reactants
- rate = K[A]x[B]y
- k is the rate constant
- A and B are reactants, [] means concentration
- X and Y are the ‘orders’ of each reactant, determined experimentally
1st Order Integrated Rate Law
ln [A]0/[A]t = Kt
2nd Order Integrated Rate Law
1/[A]t - 1/[A]0 = Kt
Zeroth Order Integrated Rate Law
[A]t - [A]0 = -Kt
Half Life
- the amount of time for concentration of a reactant to decrease to half its initial concentration
1st Order Half Life Equation
(ln 2)/k = t1/2
Activation Energy
- the energy threshold that must be reached for a reaction to occur (KJ/mol)
- the “hill” on a reaction pathway graph
Transition State
- the species formed by reactant molecules before products are generated, defined by its insignificant lifetime
Arrhenius Equation for 2 rate constants and 2 temperatures
ln (K2/K1) = - Ea/R(1/T2-1/T1)
Intermediate
- a compound that appears in a chemical mechanism but is not seen in the overall reaction
- it is generated and then consumed
- unlike transition state, it has a lifetime
Catalyst
- a substance that lowers the activation barrier of a reaction, but is not consumed by the reaction