Ch 10 Particle Forces
States of Matter Solid- Particles moving about a fixed point Liquid-Particles moving about a moving point Gas-Particles filling the volume of the container with complete random motions.
Particle Forces Affect Solubility Vapor Pressures Freezing Points Boiling Points 3
Particle Forces Intramolecular forces (Relative strength = 100) Ionic bonding Covalent bonding Interparticle forces Ion-dipole forces Dipole-dipole (Polar molecules) (relative Strength = 1) London Forces (Dispersion forces)( Nonpolar molecules) (relative strength = 1) Hydrogen Bonding (Relative strength = 10)
Ion-Ion Interactions Coulomb’s law states that the energy (E) of the interaction between two ions is directly proportional to the product of the charges of the two ions (Q1 and Q2) and inversely proportional to the distance (d) between them.
Predicting Forces of Attraction Coulombs Law indicates the increases in the charges of ions will cause an increase in the force of attraction between a cation and an anion. Increases in the distance between ions will decrease the force of attraction between them.
Size of Ions
Lattice Energy M+(g) + X-(g) ---> MX(s) The lattice energy (U) of an ionic compound is the energy released when one mole of the ionic compound forms from its free ions in the gas phase. M+(g) + X-(g) ---> MX(s)
Comparing Lattice Energies Lattice Energies of Common Ionic Compounds Compound U(kJ/mol) LiF -1047 LiCl -864 NaCl -790 KCl -720 KBr -691 MgCl2 -2540 MgO -3791
Practice Determine which salt has the greater lattice energy. MgO and NaF MgO and MgS
Lattice Energy Using Hess’s Law
Electron Affinity Cl(g) + e-(g) ---> Cl-(g) Electron affinity is the energy change occurring when one mole of electrons combines with one mole of atoms or ion in the gas phase. Step 4 in diagram on the last slide. Cl(g) + e-(g) ---> Cl-(g) ΔHEa = -349 kj/mole
Calculating U Na+(g) + e-(g) ---> Na(g) -HIE1 Na(g) ---> Na(s) -Hsub Cl-(g) ---> Cl(g) + e-(g) -HEA Cl(g) ---> 1/2Cl2(g) -1/2HBE Na(s) + 1/2Cl2(g) ---> NaCl(s) Hf Na+(g) + Cl-(g) ---> NaCl(s) U U = Hf - 1/2HBE - HEA - Hsub - HIE1
Lattice energy for NaCl.
Interactions Involving Polar Molecules An ion-dipole interaction occurs between an ion and the partial charge of a molecule with a permanent dipole. The cluster of water molecules that surround an ion in aqueous medium is a sphere of hydration.
Illustrates of Ion-Dipole Interaction
The Solution Process Bond Breaking Processes Break solute particle forces (expanding the solute), endothermic Break solvent particle forces (expanding the solvent), endothermic
The Solution Process Attractive Forces Energy released when solute solvent are attracted, exothermic Energy is released due to new attractions Ion dipole if the solute is ionic and the solvent polar. London-Dipole for nonpolar solute and polar solvent Dipole-dipole for polar solute and polar solvent
The Solution Process Theromodynamics Enthalpy Entropy ΔS (Perfect crystal, assumed to be zero) Gibbs free energy ΔG ΔG = ΔH - T ΔS ΔG < 0, spontaneous change ΔG = 0, equilibrium ΔG > 0, nonspontaneous
The Solution Process Oil dissolving in water London forces holding the oil molecules together are large do to the large surface area of the oil The hydrogen bonds holding water molecules together are large The forces of attraction of between nonpolar oil and polar water are weak at best Thus the overall process is highly endothermic and not allowed thermo chemically
The Solution Process Oil dissolving in water Entropy should be greater than zero Free energy should be greater than zero, since the process is highly endothermic Thus the overall process is nonspontaneous
The Solution Process Sodium chloride dissolving in water Large amount of energy is required to break the ionic lattice of the sodium chloride (expand solute) Large amount of energy is required to separate the water molecules to expand the solvent breaking hydrogen bonds Formation of the ion dipole forces releases a large amount of energy, strong forces (why?) The sum of the enthalpies is about +6 kJ (slightly endothermic), which is easily overcome by the entropy of the solution formation.
Water as a Solvent Water most important solvent, important to understand its solvent properties Most of the unusual solvent properties of water stem from it hydrogen bonding nature Consider the following ∆S of solution KCl →75j/K-mole LiF→-36j/K-mole CaS→-138 j/K-mole
Water as a Solvent We would expect ∆S>0 for all solutions, right? But two are negative, why? Obviously, something must be happening for the increased order. Ion-dipole forces are ordering the water molecules around the ions, thus causing more order in water i.e. less positions for water than in the pure liquid state
Water as a Solvent Smaller ions, have stronger ion dipole forces, thus pulling water closer, therefore less positions Also, ions with a charge greater than one will attract to water stronger than a one plus charge, thus more order due to less space between particles
Dipole-Dipole Interactions Dipole-dipole interactions are attractive forces between polar molecules. An example is the interaction between water molecules. The hydrogen bond is a special class of dipole-dipole interactions due to its strength.
Dipole-Dipole Forces H Cl H Cl H Cl Dipole-dipole (Polar molecules) δ– Alignment of polar molecules to two electrodes charged + and δ– Forces compared to ionic/covalent are about 1 in strength compared to a scale of 100, thus 1% δ– δ+ δ– δ+ δ– δ+ H Cl H Cl H Cl
Dipole Dipole Interactions
Hydrogen Bonding Hydrogen bonding a stronger intermolecular force involving hydrogen and usually N, O, F, and sometimes Cl Stronger that dipole-dipole, about 10 out of 100, or 10 Hydrogen needs to be directly bonded to the heteroatom Since hydrogen is small it can get close to the heteroatom Also, the second factor is the great polarity of the bond.
Hydrogen Bonding in HF(g)
Hydrogen Bonding in Water Chemistry 140 Fall 2002 Hydrogen Bonding in Water Solid ice has lower density than liquid water. H-bonding holds the ice in a rigid but open structure. Maximum density of water at 3.98 C. around a molecule in the solid in the liquid
Boiling Points of Binary Hydrides
Interacting Nonpolar Molecules Dispersion forces (London forces) are intermolecular forces caused by the presence of temporary dipoles in molecules. A instantaneous dipole (or induced dipole) is a separation of charge produced in an atom or molecule by a momentary uneven distribution of electrons.
Illustrations
Strength of Dispersion Forces The strength of dispersion forces depends on the polarizability of the atoms or molecules involved. Poarizability is a term that describes the relative ease with which an electron cloud is distorted by an external charge. Larger atoms or molecules are generally more polarizable than small atoms or molecules.
London Forces (Dispersion) Induced dipoles (Instantaneous ) Strength is surface area dependent More significant in larger molecules All molecules show dispersion forces Larger molecules are more polarizable
Instantaneous and Induced Dipoles
Molar Mass and Boiling Point Molar Mass and Boiling Points of Common Species. Halogen M(g/mol) Bp(K) Noble Gas He 2 4 F2 38 85 Ne 20 27 Cl2 71 239 Ar 40 87 Br2 160 332 Kr 84 120 I2 254 457 Xe 131 165 Rn 211
London vs Hydrogen Bonding Hydrocarbon Alcohol Molecular Formula Molar Mass Bp (oC) CH4 16.04 -161.5 CH3CH3 30.07 -88 CH3OH 32.04 64.5 CH3CH2CH3 44.09 -42 CH3CH2OH 46.07 78.5 CH3CH(CH)CH3 58.12 -11.7 CH3CH(OH)CH3 60.09 82 CH3CH2CH2CH3 -0.5 CH3CH2CH2OH 97
The Effect of Shape on Forces
Practice Rank the following compound in order of increasing boiling point. CH3OH, CH3CH2CH2CH3, and CH3CH2OCH3
Practice Rank the following compound in order of increasing boiling point. CH3OH, CH3CH2CH2CH3, and CH3CH2OCH3 MM IM Forces CH3OH 32.0 London and H-bonding CH3CH2CH2CH3 58.0 London, only CH3CH2OCH3 60.0 London and Dipole-dipole
Practice Rank the following compound in order of increasing boiling point. CH3OH, CH3CH2CH2CH3, and CH3CH2OCH3 MM IM Forces CH3OH 32.0 London and H-bonding CH3CH2CH2CH3 58.0 London, only CH3CH2OCH3 58.0 London and Dipole-dipole The order is: CH3CH2CH2CH3 < CH3CH2OCH3< CH3OH
Polarity and Solubility If two or more liquids are miscible, they form a homogeneous solution when mixed in any proportion. Ionic materials are more soluble in polar solvents then in nonpolar solvents. Nonpolar materials are soluble in nonpolar solvents. Like dissolves like
Polarity and Solubility If two or more liquids are miscible, they form a homogeneous solution when mixed in any proportion. Ionic materials are more soluble in polar solvents then in nonpolar solvents. Nonpolar materials are soluble in nonpolar solvents.
Polarity and Solubility How does polarity effect solubility? The thermodynamic argument, is that the lower the potential energy, the more stable the system. If subtracting the potential energy of the solute from the potential energy of the original solute and solvent is negative (exothermic) then solution is thermodynamically favored.
Polarity and Solubility How does polarity effect solubility? Non polar solute and solvent: The forces holding these particles together are London Dispersion forces, the weakest of all of the inter-particle forces. The strength of these forces are relative to the surface area if solute and solvent are of similar size, then about the same amount of energy is required to separate solute and solvent particles from each other. And about the same amount of energy is released when solute and solvent are attracted to each other forming a solution. Thus we predict non polar solutes and solvents should dissolve
Polarity and Solubility How does polarity effect solubility? Non polar solute and polar solvent: Considering solutes and solvents of similar surface area it should be noted that more energy is required to separate the polar solvent molecules from each other, since dipole-dipole interactions are stronger. The only interaction between a nonpolar solute and polar solvent would be London Dispersion forces, so the energy released is much less than required for separating the solvent and solute. Subtracting the potential energy of the products from reactants would give a positive (endothermic) result and the solution would be less stable than the dissolution.
Practice Rank the following compound in order of increasing boiling point. CH3OH, CH3CH2CH2CH3, and CH3CH2OCH3
Solubility of Gases in Water Henry’s Law states that the solubility of a sparingly soluble chemically unreactive gas in a liquid is proportional to the partial pressure of the gas. Cgas = kHPgas where C is the concentration of the gas, kH is Henry’s Law constant for the gas.
Henry’s Law Constants Henry’s Law Constants Gas kH[mol/(L•atm)] kH[mol/(kg•mmHg)] He 3.5 x 10-4 5.1 x 10-7 O2 1.3 x 10-3 1.9 x 10-6 N2 6.7 x 10-4 9.7 x 10-7 CO2 3.5 x 10-2 5.1 x 10-5
Terms A hydrophobic (“water-fearing) interaction repels water and diminishes water solubility. A hydrophilic (“water-loving”) interaction attracts water and promotes water solubility.
Affects of Intermolecular Forces Solubility Vapor Pressures Freezing Points Boiling Points Surface tension
Vapor Pressure Vaporization or evaporation is the transformation of molecules in the liquid phase to the gas phase. Vapor pressure is the force exerted at a given temperature by a vapor in equilibrium with its liquid phase.
Vapor Pressure
Vapor Pressure The normal boiling point of a liquid is the temperature at which its vapor pressure equals 1 atmosphere.
Vapor Pressure of Solutions What evaporates faster, sugar water or pure water? s w s w s w w w w w w w
Vapor Pressure of Solutions What evaporates faster, sugar water or pure water? w(g) w(g) w(g) s w s w s w w w w w w w
Vapor Pressure of Solutions What evaporates faster, sugar water or pure water? w(g) w(g) w(g) s w s w s w w w w w w w Pure water evaporates faster, since there are more water particles on the surface, thus lowering the average kinetic energy. Evaporation of a solution is inversely proportional to concentration.
Vapor Pressures of Solutions Roault, 1880s. Dissolved solute lowers vapor pressure of solvent. The partial pressure exerted by solvent vapor above an ideal solution is the product of the mole fraction of solvent in the solution and the vapor pressure of the pure solvent at a given temperature. PA = A P° July 2009 General Chemistry: Chapter 11 Slide 60 of 46
Vapor Pressure of Solutions Raoult’s Law Psolution = Xsolvent (Psolvent) P - vapor pressure X - mole fraction Xsolute + Xsolvent = 1
Vapor pressure of solutions What evaporates faster pure water of sugar water? What is vapor pressure Roualts Law Psol = XsolventP°solvent Equation of a straight line The slope is the P°solvent The y-intercept is zero July 2009 General Chemistry: Chapter 11 62
For a Solution that Obeys Raoult's Law, a Plot fo Psoln Versus Xsolvent, Give a Straight Line
Vapor Pressure of Solvent and Solution
An Aqueous Solution and Pure Water in a Closed Environment
Liquid-Vapor Equilibrium Chemistry 140 Fall 2002 Liquid-Vapor Equilibrium The vapor phase is richer in the more volatile component. July 2009 General Chemistry: Chapter 11 Slide 66 of 46 66
Two Volatile Liquids Ideal Solution Positive deviation Negative deviation Positive deviation exists when experimental value is larger than calculated value, weaker solute solvent attraction; more evaporation. Negative deviation exists when experimental value is smaller than calculated value; stronger solvent solute attraction; less evaporation
Fractional Distillation July 2009 General Chemistry: Chapter 11 Slide 68 of 46
Fractional Distillation July 2009 General Chemistry: Chapter 11 Slide 69 of 46
Phase Diagram of Water Note: Negative slope
Phase Diagram of Water
Phase Diagram CO2 Note: Posititve Slope
Phase Diagram CO2
Special Properties of Water Hydrogen bonding found in water gives it special properties listed below: Surface tension Capillary Rise Viscosity
Surface Tension
Surface Tension Surface Tension units J/m2
Surface Tension Adhesive forces stronger in red aqueous solution Cohesive forces stronger in mercury liquid
Capillary Rise
Viscosity
Terms Capillary action is the rise of a liquid up a narrow tube as a result of adhesive forces between the liquid and the tube and cohesive forces within the liquid. Viscosity is a measure of the resistance to flow of a fluid.
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ChemTour: Lattice Energy Click to launch animation PC | Mac Students learn to apply Coulomb’s law to calculate the exact lattice energies of ionic solids. Includes Practice Exercises.
ChemTour: Intermolecular Forces Click to launch animation PC | Mac This ChemTour explores the different types of intermolecular forces and explains how these affect the boiling point, melting point, solubility, and miscibility of a substance. Includes Practice Exercises.
Click to launch animation ChemTour: Henry’s Law Click to launch animation PC | Mac Students learn to apply Henry’s law and calculate the concentration of a gas in solution under varying conditions of temperature and pressure. Includes interactive practice exercises.
ChemTour: Molecular Motion Click to launch animation PC | Mac Students use an interactive graph to explore the relationship between kinetic energy and temperature. Includes Practice Exercises.
ChemTour: Raoult’s Law Click to launch animation PC | Mac Students explore the connection between the vapor pressure of a solution and its concentration as a gas above the solution. Includes Practice Exercises.
ChemTour: Phase Diagrams Click to launch animation PC | Mac Students use an interactive phase diagram and animated heating curve to explore how changes in temperature and pressure affect the physical state of a substance.
ChemTour: Capillary Action Click to launch animation PC | Mac In this ChemTour, students learn that certain liquids will be drawn up a surface if the adhesive forces between the liquid on the surface of the tube exceed the cohesive forces between the liquid molecules.
ChemTour: Boiling and Freezing Points Click to launch animation PC | Mac Students learn about colligative properties by exploring the relationship between solute concentration and the temperature at which a solution will undergo phase changes. Interactive exercises invite students to practice calculating the boiling and freezing points of different solutions.
ChemTour: Osmotic Pressure Click to launch animation PC | Mac Students discover how a solute can build up pressure behind a semipermeable membrane. This tutorial also discusses the osmotic pressure equation and the van’t Hoff factor.
Solubility of CH4, CH2Cl2, and CCl4 Which of the following three compounds is most soluble in water? © 2008 W. W. Norton & Company Inc. All rights reserved. A) CH4(g) B) CH2Cl2(λ) C) CCl4(λ)
Solubility of CH4, CH2Cl2, and CCl4 Consider the following arguments for each answer and vote again: A gas is inherently easier to dissolve in a liquid than is another liquid, since its density is much lower. The polar molecule CH2Cl2 can form stabilizing dipole-dipole interactions with the water molecules, corresponding to a decrease in ΔH°soln. The nonpolar molecule CCl4 has the largest molecular mass, and so is most likely to partially disperse into the water, corresponding to an increase in ΔS°soln. Answer: B
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