BackGOB Chemistry Exam 2 Study Guide: Chemical Reactions, Acids & Bases, and Hydrocarbons
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Chapter 8: Chemical Reactions and Stoichiometry
Parts and Balancing of Chemical Equations
Chemical equations represent the reactants and products in a chemical reaction. Balancing ensures the law of conservation of mass is obeyed.
Reactants are substances consumed; products are substances formed.
Balancing involves adjusting coefficients so the number of atoms of each element is equal on both sides.
Example:
Types of Chemical Reactions
Chemical reactions are classified by how reactants change into products.
Composition (Synthesis): Two or more substances combine to form one product.
Decomposition: A single compound breaks down into two or more simpler substances.
Single Displacement: An element replaces another in a compound.
Double Displacement: Exchange of ions between two compounds.
Mole Relationships and Calculations
The mole is a fundamental unit for counting particles in chemistry.
Avogadro's Number: (atoms, molecules, or ions)
Use molar ratios from balanced equations to convert between moles of reactants and products.
Example: If 2 moles of react, 2 moles of are produced.
Molar Mass and Mass Calculations
Molar mass is the mass of one mole of a substance, used to convert between mass and moles.
Molar Mass: Sum of atomic masses in a chemical formula (g/mol).
Example: Molar mass of is g/mol.
To find mass:
Stoichiometry and Limiting Reactant
Stoichiometry uses balanced equations to predict amounts of products and reactants.
Determine the limiting reactant by comparing mole ratios.
Calculate the amount of product formed from a given amount of reactant.
Dilution Equation:
Chapter 9: Energy, Equilibrium, and Acids & Bases
Potential and Kinetic Energy
Energy in chemical systems can be stored (potential) or in motion (kinetic).
Potential Energy: Stored energy due to position or composition.
Kinetic Energy: Energy of motion.
Endothermic vs. Exothermic Reactions
Reactions are classified by energy flow.
Exothermic: Release energy; products have less energy than reactants.
Endothermic: Absorb energy; products have more energy than reactants.
Reading Energy Diagrams
Energy diagrams show the energy changes during a reaction.
Activation energy is the energy required to start a reaction.
Exothermic reactions have products lower than reactants; endothermic, higher.
Chemical Equilibrium
At equilibrium, the rate of the forward reaction equals the rate of the reverse reaction.
Equilibrium Constant:
Le Châtelier’s Principle: System shifts to counteract changes in concentration, pressure, or temperature.
Acids and Bases: Definitions and Properties
Acids and bases are defined by their ability to donate or accept protons.
Bronsted-Lowry Acid: Proton (H+) donor.
Bronsted-Lowry Base: Proton (H+) acceptor.
Strong acids/bases dissociate completely; weak acids/bases only partially.
pH, Buffers, and Neutralization
pH measures the acidity or basicity of a solution.
pH Equation:
Water Ionization Constant:
Buffer: Solution that resists changes in pH; made from weak acid and its conjugate base.
Neutralization: Acid reacts with base to form water and a salt.
Acid Dissociation Constants
Acid strength is measured by the acid dissociation constant ().
Equation:
pKa:
Henderson-Hasselbalch Equation:
Table: Common Acids and Their Values
Acid | Formula | |
|---|---|---|
Phosphoric acid | H3PO4 | 7.5 × 10-3 |
Nitrous acid | HNO2 | 4.5 × 10-4 |
Hydrofluoric acid | HF | 3.5 × 10-4 |
Formic acid | HCOOH | 1.8 × 10-4 |
Acetic acid | CH3COOH | 4.3 × 10-5 |
Carbonic acid | H2CO3 | 4.3 × 10-7 |
Hydrosulfuric acid | H2S | 9.1 × 10-8 |
Dihydrogen phosphate ion | H2PO4- | 6.2 × 10-8 |
Hydrocyanic acid | HCN | 4.9 × 10-10 |
Bicarbonate ion | HCO3- | 5.6 × 10-11 |
Hydrogen phosphate | HPO42- | 2.2 × 10-13 |
Chapter 13: Hydrocarbons and Organic Chemistry
Hydrocarbon Structure and Nomenclature
Hydrocarbons are organic compounds composed of carbon and hydrogen. Their structure and naming follow IUPAC rules.
Condensed Structural Formula: Shows the arrangement of atoms without displaying all bonds.
Line Structure: Simplified representation where lines represent bonds between carbon atoms.
Alkanes: Single bonds only; Alkenes: At least one double bond; Alkynes: At least one triple bond.
Example: Ethane: CH3CH3; Ethene: CH2CH2
Physical Properties of Hydrocarbons
Hydrocarbons vary in solubility and physical properties based on structure.
Most hydrocarbons are nonpolar and insoluble in water.
Solubility decreases as the hydrocarbon chain length increases.
Isomerism and Stereochemistry
Isomers have the same molecular formula but different structures.
Structural Isomers: Differ in connectivity of atoms.
Stereoisomers: Same connectivity, different spatial arrangement.
Cis/Trans Isomers: Occur in alkenes due to restricted rotation around double bonds.
Reactions of Hydrocarbons
Hydrocarbons undergo characteristic reactions such as substitution, addition, and elimination.
Hydrogenation: Addition of hydrogen to double or triple bonds.
Halogenation: Addition of halogen atoms (Cl, Br, etc.) to hydrocarbons.
Example: Halogenation of benzene can occur at three positions: ortho, meta, para.
Appendix: Periodic Table
The periodic table organizes elements by increasing atomic number and groups elements with similar chemical properties.
Groups: Vertical columns; elements share similar properties.
Periods: Horizontal rows; properties change progressively.
Useful for determining atomic masses, valence electrons, and element classification.
Key Equations and Constants
Avogadro's Number: (atoms, molecules, or ions)
Molarity:
Dilution Equation:
Equilibrium Constant:
Water Ionization Constant:
pH Equation:
Hydronium Ion Concentration:
Acid Dissociation Constant:
pKa:
Henderson-Hasselbalch Equation:
Additional info: Some context and explanations have been expanded for clarity and completeness, including definitions, examples, and academic context for formulas and tables.