115 Intermolecular Force Worksheet Key
115 Intermolecular Force Worksheet Key
115 Intermolecular Force Worksheet Key
1. Identify the strongest intermolecular force present in pure samples of the following substances:
2. Identify the strongest intermolecular force operating in the condensed phases of the following
substances. Fully explain how you determined this.
3. Based on the intermolecular forces present, predict the relative boiling points of each of the
substances below. Arrange each series of substances in order of increasing boiling point. State
your reasons for the order you use (identify the forces and explain how they affect the boiling
point).
lowest bp: propane (CH3CH2CH3) < dimethyl ether (CH3OCH3)< ethanol (CH3CH2OH) highest bp
Dimethyl ether cannot form hydrogen bonds (no O-H bond), but is polar and has dipole-dipole forces.
Ethanol can form hydrogen bonds. propane is nonpolar, so it has only London dispersion forces. The
boiling point increases as the strength of the intermolecular forces increase:
b. Br2, Cl2, I2
All are nonpolar molecules so only London dispersion forces are present. London dispersion forces get
stronger as molar mass increases.
4. For each pair of substance identify the substance that is likely to have the higher vapor pressure.
Explain your reasoning.
a. CO2 or SO2
CO2 will have the higher vapor pressure. Vapor pressure tends to decrease as the strength of the
intermolecular forces increase. Carbon dioxide is non-polar (dispersion forces only). Sulfur dioxide is
polar (dipole-dipole forces are present).
b. CH3OH or CH3-O-CH3
CH3OCH3 will have the higher vapor pressure. Vapor pressure tends to decrease as the strength of the
intermolecular forces increase. CH3OH can hydrogen bond. CH3OCH3 is polar (bent shape around the
oxygen), so dipole-dipole forces are the strongest forces in this compound.