Average Rate
∆[concentration]/∆time
Integrated Rate Law (first-order reaction)
ln[A]t=-kt + ln[A]0
Half-life expression (second-order reaction)
t1/2=k/[A]0
Equilibrium Constant (Kc)
for the reaction aA +bB= cC +dD
Kc=[C]c x [D]d/ [A]a x [B]b
pH
pH= -log[H+]
Rate Law
Rate= k[reactant]n
Rate= k[A]n x [B]m
Integrated Rate Law (second-order reaction)
1/[A]t=kt + 1/[A]0
Arrhenius Equation
k=-Ae(-Ea/RT)
Kp (partial pressure)
*2 formulas
Kp=(PC)ceqm x (PD)deqm/ (PA)aeqm x (PB)beqm
Kp=Kc(RT)∆n
pOH
pOH=-log[OH-]
Integrated Rate Law
ln[A]t - ln[A]0=-kt
or can be written as
ln([A]t/[A]0)=-kt
Half-life expression (zero-order reaction)
t1/2=[A]0/2k
Arrhenius Equation to find Ea from a graph
ln k=-Ea/R (1/T) + lnA
Initial Change Equilibrium
I + C=E
(initial + change= equilibrium)
pKw
pKw= -logKw
Integrated Rate Law (zero-order reaction)
[A]t=-kt + [A]0
Half-life expression (first-order reaction)
t1/2=ln2/k
or 0.693/k
Arrhenius Equation to find Ea non-graphically
ln(k1/k2)=Ea/R (1/T2-1/T1)
At equilibrium
Kp=Kc when total moles of products and reactants is the same
At 25°C
pKw=-logKw