Intermolecular Forces, Solids, and Liquids

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Presentation transcript:

Intermolecular Forces, Solids, and Liquids Chapter 11

Solids, Liquids, and Gases: A Comparison--Section 11.1 The physical state that a substance is most directly influenced by the amount of kinetic energy present in the substance

Intermolecular Forces Section 11.2 The physical properties of liquids are largely dominated by the effects of intermolecular forces Vapor pressure Boiling point Melting point

Ion-Ion Interactions Strongest interaction Most often are found in ionic solids (very few ionic liquids) Strongest because it involves a full negative and positive charge (not partial)

Ion-Dipole Forces Ion-dipole forces exist between an ion with a full charge and the oppositely charged end of a dipole on a different molecule

Dipole-dipole Forces Similar to ion-dipole, but involves the alignment of dipoles of two different polar compounds The strength of dipole-dipole interactions increases as the strength of the dipole interactions increase

H-Bonding (Special Case of Dipole-Dipole Interaction) For a H-bond to form the following two criteria must be met: A covalent bond containing hydrogen must exist (N-H, O-H, or F-H bond) H-bond donor A lone pair of electrons must exist H-bond acceptor

London Dispersion Forces London dispersion forces exist for every single molecule (both polar and nonpolar) They are the only intermolecular force present for nonpolar molecules or atoms, however Strength of dispersion forces depends on the polarizability of the atom or molecule

Polarizability The polarizability of a molecule describes the extent to which the electron distribution can be altered creating an instantaneous dipole As a result, large atoms or molecules tend to have stronger dispersion forces than smaller

Predicting Boiling Points Using IMFs Identify the intermolecular forces and predict which substance of each pair has the stronger force of attraction. CF4 and CCl4 CH3OH and CHCl3 ClF and BrCl See Sample Exercise 11.3 (Pg. 447)

Phase Changes Section 11.4 As the individual particles of a solid, liquid, or gas gain or lose kinetic energy, they may go through a series of phase changes

Heat of Fusion and Heat of Vaporization Heat of fusion, Hfus, is the amount of energy required to convert a solid into a liquid (melt) Ex: H2O (s) H2O (l) Hfus = 6.01 kJ/mol Heat of vaporization, Hvap, refers to the energy required to convert a liquid into a gas or vapor Ex: H2O (l) H2O (g) Hvap = 40.7 kJ/mol

Comparison What can be said about the intermolecular forces for each of the compounds shown here?

Heat of Sublimation On rare occasions compounds will change directly from a solid into a gas Ex: CO2 (dry ice) and I2 Heat of sublimation, Hsub is therefore the sum of Hfus and Hvap Ex: CO2 (s) CO2 (g) Hsub = 25.2 kJ/mol

Heating Curves Heating curve for H2O

Enthalpy Changes Associated with Phase Changes Calculate the enthalpy change upon converting 2.30 mol of ice at -25 C to water vapor steam at 125 C under a constant pressure of 1 atm. The specific heats of ice, water, and steam are 2.03 J/g-K, 4.18 J/g-K, and 1.84 J/g-K, respectively. For H2O, Hfus = 6.01 kJ/mol and Hvap = 40.67 kJ/mol. See Sample Exercise 11.4 (Pg. 451)

Vapor Pressure Section 11.5 The vapor pressure of a liquid is the result of a dynamic equilibrium between the liquid and gas phases of that liquid Substances with very high vapor pressures are said to be very volatile Ex:

Vapor Pressure and Boiling Point A liquid will begin to boil when it’s vapor pressure equals the external pressure acting on the surface of the liquid Boiling point can be altered by a change in pressure (this is why some cooking directions include high altitude directions) The boiling point of a liquid at 1 atm (760 torr) is referred to as the normal boiling point

Structure of Solids Section 11.7 Solids can be categorized based on two criteria: Structure Crystalline solid Amorphous solid Type of bonding Covalent-network Ionic Metallic Molecular

Amorphous vs. Crystalline -- Very organized, repeating structure Amorphous -- Covalently bound, but not as organized

Bonding in Solids Section 11.8 Solids can be further classified by the types of intermolecular forces at work in the sample Molecular Covalent-network Ionic Metallic

Types of Solids Molecular Solids Covalent-Network Solids Forces at work: London dispersion, dipole-dipole, H-bonding Ex: Ar, CH4, CO2(s), etc Covalent-Network Solids Forces at work: Covalent bonds Essentially one gigantic molecule Ex: Diamond, SiO2 (quartz) Covalent-Network solids

Types of Solids (cont.) Ionic Solids Metallic Solids Made up of ionic compounds Forces at work: Ion-ion Metallic Solids Made up of metallic elements Forces at work: Metallic bonds

Metallic Bonding Metallic bonds are more than simply dispersion forces between atoms of metals Much stronger than that The bonding is best described as the valence electrons spread out over the entire sample of metal Sea of electrons