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Enthalpy equation (ΔH)
ΔH = -mcΔT/mols
m - mass
C- specific heat capacity
Ideal gas equation
pV = nRT
V - volume in m3
R - ideal gas constant
T - in K
p - in Pa
Gibbs Free Energy Equation
ΔG = ΔH - TΔS
S - entropy in kJK−1mol−1
Entropy change of a reaction
ΔS° = ΣS°(products) - ΣS°(reactants)
ALL IN J K-1mol-1
(NOT kJ)
Rate equation
Rate = K[A]^x[B]^y[C]^z
Where x y z are the order wrt A B C
Rate constant from half life
K = 0.693/t1/2
t1/2 measured in seconds
Only for FIRST ORDER reactions
Ka expression
Ka = [H+][A-] / [HA]
Kw expression (given numerical value)
Kw = [H+][OH-]
pH equation
pH = -log[H+]
[H+] = 10-pH
Eocell
Eocell = Eored - Eoox
in V
most positive Eo - least positive Eo
under standard conditions: 298K, 101kPa, 1M solutions
Charge in terms of current
Q = It
Q - in C
I - in Cs-1
charge in terms of moles of electrons
Q = F x z
z - moles of e-
F - Faraday constant (charge per mole of e-)
Nernst Equation
E = Eo + (0.059/z)log[ox]/[red]
E = non-standard electrode potential, V
z - moles of e- transferred
feasibility formula (electrochem)
ΔGo = -nFEocell
reaction is feasibly if ΔGo is NEGATIVE
n - moles of e- transferred
F - Faraday constant
G and Ecell in V
dilution equation
ViCi = VfCf
initial vol x initial conc = vol x conc after dilution
equation for number of carbon atoms from mass spectra
n = (100 x abundance of M+1 ion) / (1.1 x abundance of M+ ion)
pH directly from pKa (Henderson-Hasselbach equation)
pH = pKa + log([A-]/[HA])