Enthalpy
delta H, affected heat, release, gained
Entropy
delta s, measure of disorder or chaos
Equal
heat gain is _______ heat lost
Break
energy needed to _______ bonds
released
Energy __________ to form bonds
0.00
delta H must equal ______ for any element
-delta H
exothermic, heat is released favorable
delta H
endothermic, heat is absorbed unfavorable
Delta S universe
delta S system + delta S surroundings
delta S surroundings
-delta H/T
delta S
unfavorable, nonspontaneous
delta S
favorable spontaneous
negative
products always _______ when forming bonds
Fusion
melting, exothermic
Vaporization
boiling, endothermic
Sublimation
solid to gas, endothermic
Deposition
gas to solid (exothermic)
Gibbs free energy
ΔG = ΔH - TΔS
k>1
______ when delta G < 0 because products are favored
thermodynamically favorable
spontaneous reaction delta H < 0 and delta S > 0
Low Temps
-delta H, -delta S
High Temps
+delta H, +delta H
False
[ ] are equal
True
Rates are equal
Keq, Kc, Kp
rxn @ equilibrium and constant temp, Products/Reactants, no units, Only gases only changed by temp
Inverse
1/Keq
Doubling
[Keq]^2
Forward
Products have higher concentration, Keq > 1
Reverse
Reactants have higher concentration, Keq < 1
Q
reaction quotient, all cases not equilibrium
Equilibrium
A reaction will always shift toward
k > Q
more reactants, shift right, [R] down [P] up
K < Q
more products, shift left [R] up [P] down
Molarity or Pressure
Ice tables always stand for
I
initial molarity
C
Change
E
equilibrium
5% rule
x/initial [ ] * 100
Soluble
Compounds with Group 1 metals
Soluble
NH4+ Ammonia
Soluble
NO3-
Molar Solubility
the number of moles of solute in 1 L of a saturated solution (mol/L)
Soluble
Larger Ksp
Insoluble
Smaller Ksp
Q < Ksp
unsaturated more salt will dissolve
Q = Ksp
saturated, equilibrium
Q > Ksp
supersaturated solution, precipitate will form
Pressure Changes
Higher gas moles creates higher pressure, rxn shifts in opposite of the pressure change
Increased Pressure
rxn shifts towards fewer moles of gas
Decreased Pressure
ran shifts towards more moles of gas
H
forward with increased temp, increased Keq
H
Forward with decreased temp, increased Keq
precipitate
Ions with smaller Ksp _____ first
H
More favorable process
Entropy
A measure of disorder or randomness, + H more favorable, substances always tend towards randomness
Dissolution
the driving force behind ______ is Entropy
Delta G
delta H - T delta S
Rxn occurs
-delta H and positive delta S creates - delta G
Rxn doesn't occur
+delta H and Positive delta S creates + delta G
delta S
dissolution is always
Endo
Heat + R --> P
Exo
R ---> P + heat
Collision Theory
For a reaction to occur, the particles must collide, they must collide with the appropriate orientation, and they must collide with sufficient energy.
Increased Concentration
Faster reaction rate, increases molecules and increases collisions
Increased Temperature
Faster reaction rate, greater pressure so more collisions
Increased Pressure
Faster reaction rate from more collisions and a greater surface area
Increased Surface Area
Faster reaction rate from more collisions
Catalysts
Faster reaction rate by creating new pathways or elementary steps and doesn't change
Rate= ∆[ ]/∆t
Rate Equation
Relative Rate
Balanced Equation provides...
K
Constant
reactants
The rate law is written as a function of [ ] of all
0 order
rate is always constant, [A]t = -kt + [A]0 Concentration over time is the linear graph
1st order
rate is doubled when [A] is doubled, power of 1, ln[A]t = -kt + ln[A]0, ln concentration over time is linear
2nd order
rate is quadrupled when [A] is doubled, power of 2, 1/[A]t = -kt + 1/[A]0
M-¹(overall -1) * time-¹
Units
Half Life
t 1/2 the time required for the concentration of a reactant to decrease to one half of the original concentration
1st order
A constant half life can be justification for determining
Swamping
one reactant doesn't change and is high in excess.
0.693/k
1st order half life equation
Reaction Mechanisms
Must match balanced equation of reaction and match experimentally rate laws
Slow
rate law determined from ______ elementary step
[Reactants] or Catalysts
Rate law can only contain
∆H positive
endothermic
∆H negative
exothermic
Slow Steps
have a higher bump or highest Activation energy
Two bumps
Two step equation graphs into
Empirical Formula
1.) find mass % 2.) Convert to g 3.) Convert to moles 4.) divide by smallest mole, repeat for each element of compound
Molecular Fomula
1.) DIvide Molar mass of compound by empirical molar mass 2.) multiply equation by whole number
Percent Composition
the mass % of each element in compound, covert % to moles from grams
conductivity
how many mobile ions are present, if there are ions present
Dilution Equation
M1V1=M2V2
Ideal Gas Law
PV=nRT
P and V
Inverse p1V1=P2V2
P and T
Direct P1/T1 = P2/T2
V and T
Direct V1/T1 = V2/T2
Synthesis
A+B-->AB
Decomposition
AB->A+B
Single Replacement
A + BC --> B + AC
Double Replacement
AB + CD = AD + CB