Gen. Chem 4 Flashcards
(38 cards)
Ideal Gas Assumptions for MCAT
1) Gas molecules themselves are of negligible volume compared to the volume occupied by the gas
2) All intermolecular forces between gas molecules are negligible
THINK OF IDEAL GASES AS HAVING: NO VOLUME AND NO INTERMOLECULAR FORCES
Ideal Gas Law
PV= nRT
R= 0.0821 Latm/molK or 8.314 J/mol*K
Number of moles (n) of gas
The number of moles of gas is the only measurement of the molecules themselves we consider.
STP (Standard temperature and pressure)
- Assume that all gases are ideal AND start out at STP
Variables in the IDEAL GAS LAW at STP:
- P: 1 atm
- V: 22.4 L
- n= 1 mole
- R= 0.0821 Latm/molK or 8.31 J/mol*K
- T= 273 K (0 degrees C)
How to solve IDEAL GAS problems
- Manipulating equations
- P1V1/T1 = P2V2/T2 for the name number of moles of gas the ratio of PV/T must remain constant regardless of the changes made to the system.
Boyle’s Law
P1V1=P2V2
Assumes constant temperature
Charles’ Law
V1/T1=V2/T2
Assumes constant pressure
Van der Waals Equation
[P + a’(n/V)^2] * [(V/n) - b’]= RT
a’ is a constant that represent the actual strength of the intermolecular attractions
b’ is a constant that represents the actual volume of the molecules
PV/nRT ratio tells us which of two assumptions is the major cause of the deviation from IDEAL GAS LAW behavior:
PV/nRT > 1 it is due mostly to MOLECULAR VOLUME assumption
PV/nRT < 1 it is due mostly to INTERMOLECULAR FORCES assumption
Dalton’s Law of Partial Pressures
Ptotal=P1+P2+P3…
Adding more of gas 1 (P1) to an existing mixture of 3 gases, we have increased the partial pressure of gas 1 and the total pressure, but have had ZERO effect on the partial pressure of the other gases. Partial pressure is NOT similar to mole fraction or mass percent.
Effusion and Diffusion (Graham’s Law)
Diffusion: process by which gas molecules spread from areas of high concentration to areas of low concentration due to random motion imparted to them as a result of their KE and collisions w/ other molecules
Effusion: diffusion of gas particle through a pin hole. Pin hole is defined as a hole smaller than the average distance a gas molecule travels between collisions.
E1/E2 = sqrt(MW2)/sqrt(MW1)
E1 and E2 can represent either the effusion rate or the diffusion rate of gases 1 and 2, respectively
- Notice that the rate of effusion or diffusion is INVERSELY proportional to the molecular weight (MW) of the gas
Phase
Molecules of the same “phase”
a) Are in the same state (solid, gas, liquid)
b) have the same chemical composition
c) Are structurally homogenous (e.g., in the solid state, carbon can exist as either diamond or graphite. These meet the first two criteria, but not the third, so they are different “phases” of carbon.)
Heating Curves
- Horizontal sections represent phase changes
- If heat on x-axis, then length of first horizontal section represents the heat of fusion and the length of the second horizontal section represents the heat of vaporization.
- Slope of the lines between horizontal sections represents the inverse (DELTA T/Q) of heat capacity (Q/DELTA T) for that particular phase.
Calculating DELTA H from a heating curve
There is no change in temperature during a phase change (that is why it’s horizontal), all energy goes into breaking intermolecular forces and none goes toward an increase in temperature.
Vapor pressure
Partial pressure of the gaseous form of a liquid that exists over that liquid when the liquid and gas phases are in equilibrium
How is vapor pressure affected by temperature?
By increasing temperature, we increase vapor pressure. KE is higher in higher temperature so more molecules will have energy required to break intermolecular forces.
What two quantities are equal when a liquid boils?
When vapor pressure of the liquid equals atmospheric pressure
Raoult’s Law
Vapor Pressure w/ a NONVOLATILE solute= (mole fraction of the pure solvent, X) * (Vp of the pure solvent, VP knot)
VP=XVPknot
Total Vapor Pressure w/ a VOLATILE SOLUTE= (mole fraction of solvent * Vpknot of the solvent) + (mole fraction of the solute * Vpknot of the solute). Vp total = Vp solvent + Vp solute = XsolventVpknotsolvent + XsoluteVpknot solute
Henry’s Law
The solubility of a gas in a liquid is directly proportional to the partial pressure of the gas over that liquid
Gas solubility
Opposite of solubility of solids in liquids.
- For gases dissolved in liquids, increased temperature DECREASES solubility and decreased temperature INCREASES solubility
- Increasing the vapor pressure of a gas X over a liquid increases the solubility of gas X in that liquid
- Polar and non-polar gases easily form homogenous mixtures.
Boiling Point Elevation
Boiling point of a liquid is ELEVATED when a NON-VOLATILE solute is added according to
DELTA T = kbmi
kb= constant
m=molality
i=number of ions formed per molecule (VAN’T HOFF FACTOR)
T’T
Freezing Point Depression
The freezing point of a liquid is depressed when a NON-VOLATILE solute is added according to
DELTA T= kfmi
kf= constant (different than kb)
Osmotic Pressure
Tendency of water to move from one solution to another across a semi-permeable membrane. It is the side that will RECEIVE the water via osmosis that has the highest osmotic pressure.
Pi (greek symbol)= iMRT
i=Van Hoft factor M= molarity of solute R= gas constant T= absolute temperature