Definition: IMFs are attractive or repulsive forces between molecules. These forces are weaker than intramolecular forces (e.g., covalent bonds) that hold atoms together within a molecule.
Types of IMFs:
2.1. Van der Waals Forces: These include:
London Dispersion Forces (LDF): Present in all molecules, resulting from temporary fluctuations in electron distribution.
Strength increases with the size and shape of the molecule (more electrons, larger surface area).
Dipole-Dipole Forces: Occur between polar molecules due to permanent dipoles.
Strength depends on the magnitude of the dipole moments.
Dipole-Induced Dipole Forces: Occur when a polar molecule induces a temporary dipole in a nonpolar molecule.
2.2. Hydrogen Bonding: A special type of dipole-dipole interaction that occurs when hydrogen is bonded to highly electronegative atoms (N, O, F).
Stronger than typical dipole-dipole forces.
Essential for many biological processes and properties of water.
Impact of IMFs on Physical Properties:
3.1. Boiling Point and Melting Point: Stronger IMFs lead to higher boiling and melting points because more energy is required to overcome these forces.
3.2. Viscosity: Higher viscosity is observed in substances with stronger IMFs, as molecules are more attracted to each other, resisting flow.
3.3. Surface Tension: Stronger IMFs result in higher surface tension, as molecules at the surface are more strongly attracted to the bulk liquid.
3.4. Solubility: Substances with similar types and strengths of IMFs tend to be more soluble in each other (\"like dissolves like\").
Factors Affecting the Strength of IMFs:
4.1. Molecular Size and Shape: Larger molecules with greater surface area generally have stronger London dispersion forces.
4.2. Polarizability: The ease with which the electron cloud of a molecule can be distorted. Higher polarizability leads to stronger IMFs.
4.3. Dipole Moment: Molecules with larger dipole moments have stronger dipole-dipole interactions.
Examples and Applications:
5.1. Water (H_2O): Exhibits hydrogen bonding, leading to its high boiling point and surface tension.
5.2. Noble Gases: Only exhibit London dispersion forces; boiling points increase with atomic size (e.g., He < Ne < Ar < Kr < Xe).
5.3. Organic Molecules: Alkanes (LDF only), Aldehydes and Ketones (Dipole-Dipole forces), Alcohols (Hydrogen bonding).
Comparison Table of IMFs:
IMF Type | Present In | Strength | Example |
---|---|---|---|
London Dispersion | All molecules | Weakest | CH_4, He |
Dipole-Dipole | Polar molecules | Intermediate | CH3Cl, H2S |
Hydrogen Bonding | H bonded to N, O, F | Strong | H2O, NH3, HF |
Ion-Dipole | Ions and polar molecules | Very Strong | NaCl in water |
Note: Ion-dipole forces are typically stronger than hydrogen bonding but are not technically classified as IMFs (as they involve ions).
Here are some multiple-choice questions about intermolecular forces (IMFs), followed by their answers:
Question 1:
Which of the following is NOT a type of Van der Waals force?
(a) London Dispersion Forces
(b) Dipole-Dipole Forces
(c) Hydrogen Bonding
(d) Dipole-Induced Dipole Forces
Answer:
(c) Hydrogen Bonding
Question 2:
Which type of intermolecular force is present in all molecules?
(a) Dipole-Dipole Forces
(b) Hydrogen Bonding
(c) London Dispersion Forces
(d) Ion-Dipole Forces
Answer:
(c) London Dispersion Forces
Question 3:
Which of the following molecules is capable of forming hydrogen bonds?
(a) CH4 (b) H2S
(c) NH3 (d) C2H_6
Answer:
(c) NH_3
Question 4:
Which of the following properties is generally higher for substances with stronger intermolecular forces?
(a) Vapor Pressure
(b) Boiling Point
(c) Evaporation Rate
(d) Sublimation Rate
Answer:
(b) Boiling Point
Question 5:
Which factor primarily affects the strength of London Dispersion Forces?
(a) Dipole Moment
(b) Molecular Weight
(c) Hydrogen Bonding
(d) Ionic Charge
Answer:
(b) Molecular Weight
Question 6:
Which of the following best describes polarizability?
(a) The ability to form hydrogen bonds
(b) The measure of a molecule's dipole moment
(c) The ease with which an electron cloud can be distorted
(d) The strength of dipole-dipole interactions
Answer:
(c) The ease with which an electron cloud can be distorted
Question 7:
In which substance are dipole-dipole forces the strongest?
(a) H2 (b) CO2
(c) HCl
(d) CH_4
Answer:
(c) HCl
Question 8:
Which of the following arrangements lists the intermolecular forces in order of increasing strength (weakest to strongest)?
(a) Dipole-Dipole < London Dispersion < Hydrogen Bonding
(b) London Dispersion < Hydrogen Bonding < Dipole-Dipole
(c) London Dispersion < Dipole-Dipole < Hydrogen Bonding
(d) Hydrogen Bonding < Dipole-Dipole < London Dispersion
Answer:
(c) London Dispersion < Dipole-Dipole < Hydrogen Bonding
Question 9:
Which molecule would you expect to have the highest boiling point?
(a) CH3CH2CH3 (b) CH3CH2OH (c) CH3OCH3 (d) CH3CH2CH2CH_3
Answer:
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Answers to Multiple Choice Questions:
Question: Which of the following claims is true about intermolecular forces?
Answer: Intermolecular forces are interactions between molecules.
Question: Which of the following is not a type of intermolecular force?
Answer: Ionic bond is not a type of intermolecular force.
Question: Which of the following is not a type of intermolecular force?
Answer: Covalent bond is not a type of intermolecular force.
Question: Which of the following intermolecular forces is caused by a temporary dipole?
Answer: London dispersion is caused by a temporary dipole.
Question: Which of the following molecules is most likely to interact using hydrogen bonds? (Numbers are subscripts)
Answer: CH3NH2 is most likely to interact using hydrogen bonds.
Question: Which of the following intermolecular forces is the weakest?
Answer: London dispersion is the weakest intermolecular force.
Question: Which is the predominant intermolecular force that is present in a sample of pure water?
Answer: Hydrogen bond is the predominant intermolecular force in pure water.
Question: Which is the predominant intermolecular force that is present in a sample of pure oxygen, O2?
Answer: London dispersion is the predominant intermolecular force in pure oxygen (O_2).
Question: Which intermolecular force increases with increasing molecular mass?
Answer: London dispersion increases with increasing molecular mass.
Question: What type of intermolecular forces is found in any molecule regardless of polarity?
Answer: London dispersion is found in any molecule regardless of polarity.
Question: Which of the following pure substances forms hydrogen bonds?
Answer: HF forms hydrogen bonds.
Question: What explains the very high melting and boiling point of water?
Answer: Hydrogen bonds between water molecules explain the high melting and boiling point of water.
Question: What force explains the ability for water molecules to dissolve ionic compounds?
Answer: Ion-dipole attraction explains why water dissolves ionic compounds.
Question: Which of these physical properties typically increases when intermolecular forces increase?
Answer: All of these (Melting Point, Viscosity, Boiling Point) typically increase when intermolecular forces increase.
Question: Which of these molecules has the strongest London dispersion force? (Numbers are subscripts)
Answer: I_2 has the strongest London dispersion force.
Question: Hydrogen bonding occurs when hydrogen is bonded to N, O, or F. Which of the following would form hydrogen bonding with water molecules? (Numbers are subscripts)
Answer: NH_3 would form hydrogen bonding with water molecules.
Question: Can CH4 form hydrogen bonding? Why? (Numbers are subscripts)
Answer: No, CH_4 cannot form hydrogen bonding because the electronegativity between carbon and hydrogen is almost zero.
Question: A substance capable of hydrogen bonding has a ___ boiling point than a similar substance that doesn't hydrogen bond.
Answer: A substance capable of hydrogen bonding has a higher boiling point.
Question: Which of the following would have the highest boiling point? (Numbers are subscripts)
Answer: H_2O would have the highest boiling point.
Question: What type of intermolecular force is the result of temporary uneven distribution of electrons around molecules that result in momentary dipoles?
Answer: London dispersion is the result of temporary uneven distribution of electrons.
Question: Which of the following claims is true about the following diagram that is shown below?
Answer: The two molecules interact using hydrogen bonds (assuming the diagram shows hydrogen bonding between them).
Question: Which of the following claims is true about the following diagram that is shown below?
Answer: It shows an example of hydrogen bonds (assuming the diagram illustrates hydrogen bonding).
Question: Which of the following claims is true about the following diagram that is shown on below?
Answer: It shows an example of ion-dipole (assuming the diagram illustrates ion-dipole).
Question: What is the primary intermolecular force that occurs in pure hexane? See structure below.
Answer: London dispersion is the primary intermolecular force in pure hexane.
Question: What is the primary intermolecular force that best explains why pure ethanol has a higher boiling point than diethyl ether? See image below.
Answer: Hydrogen bonds best explain why pure ethanol has a higher boiling point than diethyl ether.
Question: Benzene, C6H6 is a carcinogen. Its structure is shown below. Considering the observation that benzene is only sparingly soluble in water, which of the following best describes the intermolecular forces of attraction between water and benzene?
Answer: There are dipole-induced dipole and London dispersion interactions between water and benzene.
Question: Analyze each of the following Lewis structures. Which of these molecules is the least soluble in water? (The numbers are subscripts)
Answer: CH3CH2CH2CH3 is the least soluble in water.
Question: On the basis of molecular structure and bond polarity, which of the following compounds is most likely to have the greatest solubility in water? (The numbers are subscripts)
Answer: NH_3 is most likely to have the greatest solubility in water.
Question: Which of the following substances has the greatest solubility in pentane, CH3CH2CH2CH2CH3? (The numbers are subscripts)
Answer: CCl4 has the greatest solubility in pentane (CH3CH2CH2CH2CH3).
Question: Which of the following ions would interact the strongest with water? (The + signs are charges)
Answer: Li^+ would interact the strongest with water.
Question: Which of the following ions would interact the weakest with water