IM Forces Forces Between Particles in Solids and Liquids • Ionic compounds – Attractive forces between oppositely charged ions hold ionic compounds together. – Ionic bonds are the strongest interparticle force. – Smaller the ion and the larger the charge on the ion the stronger the attractive forces among the ions Ionic Bonding Forces Between Particles in Solids and Liquids • Forces between molecular compounds – Intermolecular (IM) forces between molecules attract molecules to each other in the liquid and solid state. • IM forces are very weak as compared to ionic or covalent bonds States of Matter IM Forces Three types of IM Forces 1. Dipole-dipole force 2. Hydrogen “bonding” 3. London dispersion forces Interparticle Forces and Physical Properties • The stronger the attractive forces between particles in a liquid or solid, the – Higher the: • • • • Melting point Boiling point Surface tension Viscosity – Lower the: • Vapor pressure IM Forces • Dipole-dipole forces – Attractive forces between oppositely charged dipoles. – Dipole-dipole forces are found between polar compounds. • The more polar the compound the stronger the dipole-dipole force. IM Forces • Hydrogen “bonds” – Attractive force between a d+ H bonded to an O, N, or F and a d- O, N, or F generally on another molecule. • Really a relatively strong dipole-dipole force – Hydrogen bonding is the strongest of the IM forces. – H bonding is very important in water and in many biological molecules. • Hydrogen “bond” is a weak attractive force between a d + hydrogen and a d- O, N, or F in a second polar bond London Dispersion Forces • London Dispersion force – Very weak and short-lasting attractive forces between temporary dipoles • See figure 10.5 – Weakest of the IM forces London Dispersion Forces • London Dispersion forces – Found between all molecules in liquid/solid state. • Of greatest significance in nonpolar molecules as it’s the only IM force between nonpolar molecules – The larger the molecule the stronger the dipersion forces. Dispersion Forces Occur between every compound and arise from the net attractive forces amount molecules which is produced from induced charge imbalances The magnitude of the Dispersion Forces is dependent upon how easily it is to distort the electron cloud. The larger the molecule the greater it’s Dispersion Forces are. Dispersion Forces and Molecular Shape • Elongated ['i:lɔŋɡeitid, i'lɔŋ-] molecules have higher dispersion forces分散力than compact [kəm'pækt, 'kɔmpækt]简洁 molecules • Ringed structures have higher dispersion forces than straight chain molecules. – Consider: • Hexane • Cyclohexane • 2,2 – dimethyl butane Interparticle Forces • Weakest to Strongest: Intermolecular forces – all relatively weak London dispersion forces Dipole-dipole force Hydrogen Bonding Ionic bond - BY FAR THE Strongest: - not an IM Force Properties of Liquids • Freezing and boiling point • Surface tension • Capillary action • Viscosity [vi'skɔsəti]粘性,[ Which are directly related to the strength of the IM forces present between molecules? Change of State • Normal Freezing/Melting point – temperature at which the liquid and solid state co-exist at 1 atm pressure • Normal boiling point – temperature at which the liquid and gaseous state co-exist at 1 atm pressure • Predict the relative BP of: – Methane, acetone, methanol, ethanol, NaCl Surface Tension • Surface tension – Resistance of a liquid to increase its surface area – Measure of the energy needed to break the IM forces at the surface Capillary Action • Capillary action – Spontaneous rising of a liquid in a narrow tube • Related terms: – Cohesive forces – attractive forces among like molecules – Adhesive forces – attractive forces among dislike molecules See Figure 10.7, page 444 Concave meniscus Adhesion > Cohesion Convex meniscus Cohesion > adhesion Viscosity • Viscosity – resistance of a liquid to flow – Highly viscous liquids are thick (syrupy) – Consider relative viscosity of: • Propanol • Glycerol Graphite • Layers of ringed carbon structures – Each C is bonded to 3 other C – Each C is sp2 hybridized Diamond • A diamond is a gigantic molecule, each C atom is bonded to 4 other C atoms • Each C is sp3 hybridized A phase diagram summarizes the conditions at which a substance exists as a solid, liquid, or gas. Phase Diagram of Water 11.9 11.9 CH 11: Properties of Solutions 1. Describing Solutions – concentration units 2. Energetics of solution formation 3. Colligative Properties of solutions • • • • BP elevation FP depression Osmotic pressure Vapor Pressure Terms • Solution – homogeneous mixture • Solvent – generally the larger component of the solution – Determines the physical state of the solution • Solute – generally the smaller component of the solution – Solute is dispersed in the solvent Solution Composition • Concentrated solution – relatively large amount of solute • Dilute solution – relatively small amount of solute Solution Composition • Unsaturated solution –solution with less than the maximum amount of solute that will normally dissolve at a given temperature • Saturated solution - solution with maximum amount of solute that will normally dissolve at a given temperature Solution Composition • Super-saturated solution - solution with more than the maximum amount of solute that will normally dissolve at a given temperature Concentration Units Molarity (M) = moles solute/Liters solution Molality (m) = moles solute/kg solvent Mass % = Mass solute/mass solution x100% Mole fraction (cA) = moles A/total moles Practice! • Start by writing definitions for the concentration units M= m= Mass % = Mole fraction = Starting with Molarity Solution: – 3.75 M H2SO4 solution with a density of 1.23 g/mL Calculate: – Mass % – Molality – mole fraction of H2SO4 Starting with Masses Solution: – A solution is made by combining 66.0 grams of acetone (C3H6 O) with 146.0 grams of water. – Solution has a density of 0.926 g/mL Calculate: – – – – Molarity – need volume of solution Mass % Molality Mole fraction of acetone Starting with Mass % Solution: – 35.4 % H3PO4 – Density of 1.20 g/mL Calculate: – Molarity – Molality – Mole fraction of H3PO4 Starting with Molality Solution: – 2.50 m HCl solution – Density of 1.15 g/mL Calculate: – Molarity – need _______ – Mass % – Mole fraction of HCl Solution Formation Formation of a solution involves 3 steps 1. Separate the solute particles • expand the solute 2. Separate the solvent particles • Expand the solvent 3. Form the solution – Solute and solvent interact Solution Formation • Each step of solution formation involves energy and has a DH. DH1 = energy needed to separate the solute DH2 = energy needed to separate the solvent DH3 = energy released when solution forms Solution Formation DHsolution = DH1 + DH2 + DH3 Solutions form when the DHsolution is a small value – see page 492 Factors Impacting Solubility • Structure – like dissolves like – #38 on page 520 Factors Impacting Solubility • Pressure – Pressure has little impact on the solubility of liquids and solids – Pressure has a significant impact on the solubility of gases in a liquid • The higher the pressure of gaseous solute above a liquid the higher the concentration of the gas in the solution Henry’s Law • Henry’s Law: C = kP C = Concentration of dissolved gas k = solution specific constant P = partial P of the solute gas above the solution • No calculations required. Temperature and Solubility • Temperature has variable effects on the amount of solid that will dissolve in an aqueous solution! – See figure 11.6 page 496 • Solutes do dissolve more rapidly at higher temperatures Temperature and Solubility • The solubility of a gas in water decreases as temperature increases. – See figure 11.7 on page 496 – Thermal pollution – read the story on page 497 when you get a chance Vapor Pressure of Solutions • See Raoult’s Law on page 498 • Psolution = csolvent P0 solvent Colligative Properties • Colligative properties – properties of a solution that depend upon the amount of dissolved solute, not the identity of the solute. • Freezing point depression • Boiling point elevation • Osmotic Pressure • Note: I will be weaving section 11.7 and the van’t Hoff factor (i) into my consideration of these properties and not consider it separately. Colligative Properties D FP = Kf m i D BP = Kb m i See page 505 for needed constants 1. Calculating the bp or fp of a solution 2. Calculating the molar mass of a solute from fp or bp data Osmotic Pressure • Osmotic Pressure (P) is often used to determine the molar mass of large biological molecules – See figure 11.17 on page 508 P = MRTi