Chemistry A Molecular Approach AP Edition Chapter 12 Solutions
12.1 Thirsty Solutions: Why You Shouldn't Drink Seawater
- Seawater draws water out of the body
- Seawater is a "thirsty" solution
- Seawater draws water toward itself
- A solution is a homogeneous mixture of two or more substances/components
- The majority component is the solvent
- The minority component is the solute
- Solutions form because of intermolecular forces
- Molecules want to form uniform mixtures over pure substances
- If a person drinks seawater, the water in their body will flow out in order to make the seawater uniform
- As the concentrations become more uniform, the solutions starts to dilute
12.2 Types of Solutions and Solubility
- Gaseous solutions are two gases mixed together
- Liquid solutions can be a gas and a liquid, a liquid and a liquid, or a solid and a liquid
- Solid solutions are two solids
- In aqueous solutions, water is the solvent and some other solid, liquid, or gas in the solute
- Soluble means the solute will dissolve in the solvent
- Insoluble means the solute will not dissolve in the solvent
- Solubility is the amount of substance that will dissolve in a given solvent
- Solubility depends on mixing and intermolecular forces
Nature's Tendency toward Mixing: Entropy
- Although most situations tend to lower potential energy, this is not true for all solutions
- Mixing two ideal gases does not lower their potential energy
- Entropy measures energy randomization or energy dispersal
- Energy dispersal happens in gases
- Energy dispersal happens when things are going from hot to cold in order to heat up the other end
The Effect of Intermolecular Forces
- Intermolecular forces can allow for or prevent solution formation
- Intermolecular forces exist in three ways: Solvent-solute, Solvent-solvent, and Solute-solute
- Solvent-solute is the interaction between solvent and solute particles
- Solvent-solvent is the interaction between a solvent particle and another solvent particle
- Solute-solute is the interaction between a solute particle and another solute particle
- Miscibility is the ability to be soluble in all proportions
- If the solvent-solute interactions are greater than the solvent-solvent and solute-solute interactions a solution will form
- If the solvent-solute interactions are equal to the solvent-solvent and solute-solute interactions a solution will form
- If the solvent-solute interactions are less than the solvent-solvent and solute-solute interactions a solution may or may not form
- Solution formation does depend on disparity
- The general rule of thumb is that "like dissolves like"
- Polar solvents tend to dissolve polar or ionic solutes
- Nonpolar solvents tend to dissolve nonpolar solutes
12.3 Energetics of Solution Formation
- When heat is released the process is exothermic (-)
- When heat is absorbed the process is endothermic (+)
- Separating a solute is always endothermic because energy is required to break IM forces
- Separating a solvent is always endothermic because energy is required to break IM forces
- Mixing solute particles with solvent particles is always exothermic because energy is released when interactions occur
- The enthalpy of a solution is the sum of the enthalpy changes in each step
- If the sum of the endothermic processes is equal to the exothermic process the enthalpy is 0
- If the endothermic processes are less than the exothermic process the enthalpy will be negative. The solution will be exothermic
- If the endothermic processes are greater than the exothermic process the enthalpy will be positive. The solution will be endothermic
- If the enthalpy of a solution is too large a solution will not form
Aqueous Solutions and Heats of Hydration
- The heat of hydration is the enthalpy change that occurs when 1 mole of the gas solute dissolves in water
- The enthalpy of hydration is always largely negative for ionic compounds
- If the enthalpy of the solute is less than the enthalpy of hydration, the enthalpy of the solution is negative. The solution will be exothermic
- If the solution is exothermic the solution will feel warm to the touch
- If the enthalpy of the solute is greater than the enthalpy of hydration, the enthalpy of the solution is positive. The solution will be endothermic
- If the solution is endothermic the solution will feel cool to the touch
- If the enthalpy of the solute is about equal to the enthalpy of hydration, the enthalpy of the solution is about 0. It will not be endo or exothermic
- If the enthalpy of the solution is about 0, there is no noticeable change in temperature
12.4 Solution Equilibrium and Factors Affecting Solubility
- The dissolution of a solute in a solvent is an equilibrium process
- Initially, the rate of dissolution is faster than the rate of recrystallization
- As the concentration of the dissolved solute increases, the rate of recrystallization increases
- When the rate of dissolution and recrystallization are equal, dynamic equilibrium is reached
- In a saturated solution all solute has been dissolved. If more solute were to be added, it would not dissolve
- Saturated solutions are in dynamic equilibrium
- In an unsaturated solution not all of the solute has been dissolved. If more solute was added it would dissolve
- Unsaturated solutions are not at dynamic equilibrium
- A supersaturated solution can contain more solute than it is supposed to
- Supersaturated solutions are unstable
The Temperature Dependence of the Solubility of Solids
- Solubility of a solid in water strongly depends on temperature
- The solubility of most solids increases with an increase in temperature
- Recrystallization is a way to purify a solid
- Recrystallization is used to make rock candy
Factors Affecting the Solubility of Gases in Water
- Solutions of gases dissolved in water are common
- The solubility of a gas in a liquid are temperature and pressure dependent
The Effect of Temperature
- The solubility of gases in liquids decrease with an increase in temperature
- There is an inverse relationship between gas solubility and temperature
- Warm temperature results in lower oxygen concentration
The Effect of Pressure
- The higher the pressure of a gas above a liquid, the more soluble the gas is in the liquid
- Henry's law quantifies the solubility of gas with increasing pressure
- Sgas = kHPgas
- Sgas is the solubility of the gas in M
- kH is the constant of proportionality (Henry's law constant)
- kH depends in the specific solute and solvent (also temperature)
- Pgas is the partial pressure of the gas in atm
12.5 Expressing Solution Concentration
- A dilute solution contains a small amount of solute compared to the solvent
- A concentrated solution contains large amounts of solute compared to the solvent
- Concentration can be found with molarity, molality, parts by mass, parts by volume, mole fraction, and mole percent
Molarity
- The unit for molarity is M
- M = amount of solute / volume of solution
- The amount of solute is always in moles
- The volume of the solution is always in L
- Molarity is often used when making, diluting, or transerfing solutions
- Molarity depends on volume. Since volume depends on temperature, molarity is temperature dependent
Molality
- Molality is showed with m
- m = amount of solute / mass of solvent
- The amount of solute is always in moles
- The mass of the solvent is always in kg
- Molality is used when comparing concentrations over a range of temperatures
Parts by Mass and Parts by Volume
- Parts by mass is the ratio of the mass of solute to the mass of the solution. It is then multiplied by a multiplication factor
- (Mass solute / Mass solution) x multiplication factor
- For percent by mass, the multiplication factor is 100
- Percent by mass = (mass solute / mass solution) x 100%
- Percent means per hundred. A solution with a 14% concentration contains 14g solute for 100g solution
- Dilute solutions typically use parts per million (ppm) or parts per billion (ppb)
- Parts per million have a multiplication factor of 10^6
- Parts per billion has a multiplication factor of 10^9
- ppm = (mass solute / mass solution) x 10^6
- ppb = (mass solute / mass solution) x 10^9
- Parts by volume is a ratio of volume of solute to volume of solution. It is then multiplied by a multiplication factor
- (Volume solute / Volume solution) x multiplication factor
- A solution with 22% volume has 22mL solute for 100mL solution
Using Parts by Mass (or Parts by Volume) in Calculations
- Parts by mass or parts by volume can be used as a conversion factor
Mole Fraction and Mole Percent
- Mole fraction is represented by Xsolute
- Xsolute = amount solute / total amount of solute and solvent
- nsolute / nsolute + nsolvent
- Both are represented in moles
- Mole percent is the mole fraction times 100%
- mol % = Xsolute x 100%
12.6 Colligative Properties: Vapor Pressure Lowering, Freezing Point Depression, Boiling Point Elevation, and Osmotic Pressure
- Colligative properties depend on the number of particles dissolved in a solution
- Colligative properties do not depend on the type of particle
- Colligative properties include vapor pressure lowering, freezing point depression, boiling point elevation, and osmotic pressure
- When 1 mole of a nonelectrolyte is dissolved in water, 1 mole of dissolved particles is formed
- When 1 mole of an electrolyte is dissolved in water, more than 1 mole of dissolved particles is formed
Vapor Pressure Lowering
- Vapor pressure of a liquid is the pressure of gas above the liquid when they are in dynamic equilibrium
- The vapor pressure of a the solution is lower than the vapor pressure of a pure solvent
- When a nonvolatile solute is added, the rate of vaporization is slower than the rate of the pure solvent (rate if condensation is greater)
- By the time the rates are equal again, the concentration of solvent molecules has decreased
- A concentrated solution has the ability to draw a solvent to itself
- Nature's tendency to mix causes a solution to become less and less concentrated
- Raoult's law quantifies the vapor pressure of a solution
- Psolution = XsolventPsolvent
- Psolution is the vapor pressure of the solution
- Xsolvent is the mole fraction of the solvent
- Psolvent is the vapor pressure of the pure solvent at the same temperature
- Vapor pressure lowering is the difference in vapore pressure between the pure solvent and the solution
- Vapor pressure lowering = Psolvent - Psolution
- The vapor pressure lowering is directly proportional to the mole fraction of the solute
Vapor Pressure of Solutions Containing a Volatile (Nonelectrolyte) Solute
- If a solution contains a volatile solvent and volatile solute, both affect the vapor pressure of the solution
- An ideal solution will follow Raoult's law at all concentrations (for both solute and solvent)
- In an ideal solution the solute-solvent interactions are equal to solvent-solvent interactions
- In a nonideal solution, solute-solvent interactions are either stronger or weaker than solvent-solvent interactions
- If solute-solvent interactions are stronger, the solute will stop the solvent from vaporizing quickly
- If a solution is dilute, Raoult's law works as an approximation
- If a solution is not dilute, the effect and vapor pressure will be less than Raoult's predicted amount
- If solute-solvent interactions are weaker, the solute will allow more vaporization
- A solution that is not dilute will have a large effect and the vapor pressure will be greater than Raoult's predicted amount
Freezing Point Depression and Boiling Point Elevation
- Vapor pressure lowering occurs at all temperatures
- A lower melting point is called freezing point depression
- A higher boiling point is called boiling point elevation
- The freezing point of a solution is lower than the freezing point of a pure solvent
- Tf = m X Kf
- Tf is the change in temperature of the freezing point in Celsius (usually a positive number)
- m is molality of solution in moles solute per kilogram solvent
- Kf is the freezing point depression constant for the solvent
- The boiling point of a solution is higher than the boiling point of a pure solvent
- Tb = m X Kb
- Tb is the change in temperature of the boiling point in Celsius
- m is the molality of the solution in moles solute per kilogram solvent
- Kb is the boiling point of elevation constant for the solvent
Osmotic Pressure
- Osmosis is the flow of solvent from a solution of a lower solute concentration to one of a higher solute concentration
- Concentrated solutions draw solvent from more dilute solutions
- The semipermeable membrane allows some substances to pass through, but not all
- Osmotic pressure is the pressure required to stop osmotic glow
- Osmotic pressure = MRT
- M is molarity of the solution
- T is the temperature (in Kelvin)
- R is the ideal gas constant
12.7 Colligative Properties of Strong Electrolyte Solutions
- Van't Hoff factor is the ratio of moles or particles in a solution to moles of formula units dissolved
- Van't Hoff factor is represented with and i
- i = moles of particles in solution / moles of formula units dissolved
- The expected factor only occurs in very dilute solutions
- The expected values do not occur because some ions pair in a solution
- To calculated the different properties for an ionic solution, multiple the m by i
- Tf = im X Kf
- Tb = im X Kb
- Osmotic pressure = iMRT
Strong Electrolytes and Vapor Pressure
- An electrolyte solutions has a greater freezing point depression than a solution that is a nonelectrolyte solution of the same concentration
- Vapor pressure of an electrolyte solution is greater than that of a nonelectrolyte solution
Colligative Properties and Medical Solutions
- Osmotic pressures that are greater than body fluids are hyperosmotic
- Hyperosmotic solutions take water out of cells and tissues
- Osmotic pressures that are less than body fluids are hyposmotic
- Hyposmotic solutions pump water into cells
- Isosmotic solutions are normal
12.8 Colloids
- Colloidal dispersion, or a colloid, is a mixture when the substance is dispersed evenly but not fully dissolved
- Milk, fog, smoke, and whipped cream are all colloids
- Colloids are determined by the size of the particles
- If the diameter is between 1nm and 1000nm, the mixture is a colloid
- Colloid particles move in what is called the Brownian motion
- In micelles, the nonpolar end interacts with the center of a sphere to maximize interactions
- Micelles structure scatter light
- Scattering light is called the Tyndall effect