BackComprehensive Study Guide: General Chemistry II Final Exam Topics
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Solutions
Concentration and Molarity
Concentration describes the amount of solute dissolved in a given quantity of solvent or solution. Molarity (M) is the most common unit, defined as moles of solute per liter of solution.
Formula:
Example: To prepare 1.0 L of 0.5 M NaCl, dissolve 0.5 mol NaCl in enough water to make 1.0 L of solution.
Particle Diagrams: Visual representations showing the relative number of solute and solvent particles in a solution.
Colligative Properties
Colligative properties depend on the number of solute particles, not their identity. Key properties include:
Freezing Point Depression:
Boiling Point Elevation:
Vapor Pressure Lowering: Addition of solute lowers the vapor pressure of the solvent.
Where: = van 't Hoff factor, and = constants, = molality.
Example: Adding salt to ice lowers its freezing point, causing ice to melt at lower temperatures.
Enthalpy of Solution and Intermolecular Forces
The enthalpy of solution () is the heat absorbed or released when a solute dissolves. Intermolecular forces (IMFs) such as hydrogen bonding, dipole-dipole, and London dispersion forces affect solubility and solution properties.
Example: Ionic compounds dissolve in water due to ion-dipole interactions.
Kinetics
Rate of Reaction
The rate of reaction measures how quickly reactants are converted to products, typically as change in concentration over time.
Formula:
Example: If [A] decreases from 1.0 M to 0.5 M in 10 s, rate = 0.05 M/s.
Order of Reaction
The order of reaction indicates how the rate depends on reactant concentrations. Determined experimentally.
Example: Rate law:
Rate Constants
The rate constant (k) is a proportionality constant in the rate law, specific to a reaction at a given temperature.
Units depend on overall reaction order.
Activation Energy and Reaction Progress Diagrams
Activation energy (E_a) is the minimum energy required for a reaction to occur. Reaction progress diagrams show energy changes during a reaction.
Arrhenius Equation:
Equilibria
Equilibrium and Equilibrium Constants
Chemical equilibrium occurs when the rates of forward and reverse reactions are equal. The equilibrium constant (K) expresses the ratio of product to reactant concentrations at equilibrium.
Expression:
ICE Tables
ICE (Initial, Change, Equilibrium) tables help calculate equilibrium concentrations.
Example: For , set up initial, change, and equilibrium rows to solve for unknowns.
Relationship Between and
uses concentrations; uses partial pressures. For gases:
= change in moles of gas
Reaction Quotient (Q) and Le Chatelier’s Principle
The reaction quotient (Q) predicts the direction a reaction will proceed to reach equilibrium. Le Chatelier’s Principle states that a system at equilibrium responds to disturbances by shifting to counteract the change.
Example: Increasing reactant concentration shifts equilibrium toward products.
Aqueous Equilibria
Acids, Bases, and Conjugates
Strong acids/bases dissociate completely; weak acids/bases only partially. Conjugate acid-base pairs differ by one proton.
Example: (base) and (conjugate acid)
pH Calculations Using and
and are equilibrium constants for acids and bases. pH is calculated as:
Use ICE tables and / to solve for [H+] or [OH-].
Solubility Product () and Molar Solubility
describes the solubility of sparingly soluble salts. Molar solubility is the number of moles of solute that dissolve per liter.
Example: For ,
Thermodynamics
Entropy Changes
Entropy (S) measures disorder. Increases with more particles, higher temperature, or phase changes (solid → liquid → gas).
Example: Dissolving salt in water increases entropy.
Gibbs Free Energy and Spontaneity
Gibbs free energy (G) predicts spontaneity:
If , the process is spontaneous.
Relationship Between and
Nuclear Chemistry
Isotopes
Isotopes are atoms of the same element with different numbers of neutrons.
Example: , , and are isotopes of carbon.
Types of Nuclear Changes
Includes alpha decay, beta decay, gamma emission, and nuclear fission/fusion.
Example: (beta decay)
Half-Life Calculations
Half-life (t1/2) is the time for half of a radioactive sample to decay.
Oxidation-Reduction (Redox)
Balancing Redox Equations
Redox reactions involve electron transfer. Equations are balanced by separating into half-reactions and balancing mass and charge.
Example:
Cell Voltage in Voltaic Cells
Voltaic (galvanic) cells generate electricity from spontaneous redox reactions. Cell voltage (Ecell) is calculated from standard reduction potentials.
Nernst Equation
The Nernst equation calculates cell potential under nonstandard conditions:
Organic Compounds
Hydrocarbon Isotopes
Hydrocarbons are compounds of hydrogen and carbon. Isotopes refer to molecules with different isotopic forms of carbon or hydrogen.
Example: Methane with instead of .
Functional Groups
Functional groups are specific groups of atoms within molecules that determine chemical reactivity.
Examples: Alcohol (-OH), carboxylic acid (-COOH), amine (-NH2), alkene (C=C), alkyne (C≡C).
Sample Structure: The diagram provided shows a simple hydrocarbon chain, likely representing an alkane.
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