chem equations Flashcards
(19 cards)
Boyle’s Law
- Gas law that state that P (atm) and V (L) are INVERSELY proportional under constant temp and mols
P1V1 = P2V2
Charles’ Law
- Gas law that state that V (L) and temp (K) are DIRECTLY proportional under constant pressure and mols
V1/T1 = V2/T2
Avogadro’s Law
- Gas law that state that V (L) and n (mols) are DIRECTLY proportional under constant temp and pressure
V1/n1 = V2/n2
Gay-Lussac’s Law
- Gas law that state that P (atm) and V (L) are DIRECTLY proportional under constant volume and mols
P1/T1 = P2/T2
Combined Gas Law
P1V1 / n1T1 = P2V2 / n2T2
5 postulates of the Ideal Gas Law
- Particles in a gas are in constant, random motion
- Combined volume of particles in negligible
- Particles exert no force on one another
- Gas molecule collisions are completely elastic (no IMF)
- All gases have the same average kinetic energy at a given temperature (avg kinetic energy of particles is proportional to the temp in Kelvins)
Ideal Gas Law formula
PV = nRT
R can be either, depends on the units of pressure (atm or kPa)
What is the Standard Temperature and Pressure (STP)?
Standard temp is 273 K, standard pressure is 1 atm, for an ideal gas
1 mol of gas at STP = 22.4 L
Daltons Law of Partial Pressure
Ptotal = P1 + P2 + P3 +…
(sum of all the partial pressures of gases)
P1 = X1(Ptotal)
- X1 is the mole fraction of gas 1 (mols of gas 1/total mols)
Gas density
d = m/V = PM/RT
Where:
d = density (p)
m = mass
V = voume
P = pressure
M = molar mass
R = ideal gas constant
T = temperature (K)
Graham’s Law of Effusion
- says the rate of effusion of a gas is inversely proportional to the square root of its molar mass
- LIGHT gases diffuse and effuse much FASTER than heavier gases
r1/r2 = sqrt(M2/M1)
where:
r1 = effusion rate of gas 1
r2 = effusion rate of gas 2
M1 = molar mass of gas 1
M2 = molar mass of gas 2
Freezing-Point Depression
- a drop in the minimum temp a which a substance freezes
- caused when a non-volatile solute is added
- means that a SOLUTION has a lower freezing point than a pure solvent
ΔTf = - kf i m
ΔTf = amount freezing point decreases
Kf = solvents freezing point depression constant
i = solute’s Van’t Hoff factor
m = molal concentration of solution
Osmotic Pressure
the pressure it would take to stop osmosis
Π = iMRT
Π = osmotic pressure (atm)
i = van’t Hoff factor
M = molarity of solution
R = universal gas constant (0.0821 L atm/K mol)
T = temperature in Kelvin
Boiling-point elevation
- the phenomenom that the boiling point of a liquid (a solvent) will be HIGHER when a non-volatile solute is added
- means that a solution has a higher bp than a pure solvent
ΔTb = kb i m
ΔTb = amount boiling point increases
kb = solvents boiling point elevation constant
i = solutes van’t hoff factor
m = molal concentration of solution
Raoult’s Law
calculating new vapour pressure
PA = XA P°A
(subscript A)
PA = vapour pressure of solution
XA = mole fraction of solvent
P°A = pure vapour pressure of solvent
Vapor pressure and boiling point relationship
Generally :
increase in vapor pressure = increase in bp
adding solute:
decrease vapour pressure = increase in bp
molality
m = mols solute/kg of solvent
molarity
M = mols solute/L of solution
solution is solute and solvent combined
Beer’s Law
A = εlc
A = abosrbance
ε = molar absorptivity concept (M^-1 cm^-1)
l = path length
c = concentration of solution (M)