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 present before the reaction; products are formed after the reaction.
Balancing involves adjusting coefficients so the number of atoms of each element is equal on both sides.
Example:
Types of Chemical Reactions
Chemical reactions can be classified by how reactants are transformed into products.
Composition (Synthesis): Two or more substances combine to form one product.
Decomposition: A single compound breaks down into two or more products.
Single Displacement: An element replaces another in a compound.
Double Displacement: Exchange of ions between two compounds.
Combustion: A substance reacts with oxygen, releasing energy, usually as heat and light.
Example: (combustion)
Stoichiometry and Mole Calculations
Stoichiometry involves quantitative relationships in chemical reactions.
Mole: The amount of substance containing particles (Avogadro's number).
Molar Mass: The mass of one mole of a substance (g/mol).
Conversions: Use molar mass to convert between grams and moles.
Example: To find moles in 18g of water:
Limiting Reactant and Theoretical Yield
The limiting reactant determines the maximum amount of product formed.
Calculate moles of each reactant; the one producing the least product is limiting.
Theoretical yield: The maximum amount of product possible from limiting reactant.
Example: If 2 mol H2 and 1 mol O2 react, H2 is limiting for .
Dilution Calculations
Dilution involves adding solvent to decrease concentration.
Use the formula:
Example: To dilute 50 mL of 2 M solution to 1 M:
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.
Breaking bonds requires energy (endothermic); forming bonds releases energy (exothermic).
Endothermic vs. Exothermic Reactions
Endothermic: Absorbs heat; products have higher energy than reactants.
Exothermic: Releases heat; products have lower energy than reactants.
Energy diagrams show the energy change during a reaction.
Chemical Equilibrium
At equilibrium, the rate of the forward reaction equals the rate of the reverse reaction.
Equilibrium constant (K):
Le Châtelier’s Principle: If a system at equilibrium is disturbed, it will shift to counteract the disturbance.
Acids and Bases
Bronsted-Lowry definition: Acids donate protons (H+), bases accept protons.
Strong acids/bases: Completely ionize in water (e.g., HCl, NaOH).
Weak acids/bases: Partially ionize (e.g., acetic acid, ammonia).
Acid dissociation constant (Ka):
pH:
pKa:
Buffer: A solution that resists pH change, made from a weak acid and its conjugate base.
Neutralization: Acid + base → salt + water.
Acid-Base Calculations
Water dissociation constant:
Relationship:
pH and pOH:
Henderson-Hasselbalch equation:
Acid Dissociation Constants Table
The following table lists common acids and their values, which indicate acid strength (lower = weaker acid):
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 | HCO2H | 1.8 × 10-4 |
Acetic acid | CH3COOH | 1.8 × 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 Basics
Hydrocarbons: Structure and Properties
Hydrocarbons are organic compounds consisting of only carbon and hydrogen.
Alkanes: Saturated hydrocarbons with single bonds (C–C).
Alkenes: Unsaturated hydrocarbons with at least one double bond (C=C).
Alkynes: Unsaturated hydrocarbons with at least one triple bond (C≡C).
Solubility: Hydrocarbons are generally nonpolar and insoluble in water.
Structural Formulas and Isomerism
Condensed structural formula: Shows the arrangement of atoms without all bonds.
Line structure: Simplified organic structure where lines represent bonds between carbon atoms.
Isomers: Molecules with the same molecular formula but different structures.
Cis-trans isomerism: Occurs in alkenes due to restricted rotation around double bonds.
Naming and Identifying Hydrocarbons
Use IUPAC rules to name hydrocarbons based on the longest carbon chain and substituents.
Identify the structure from the name and vice versa.
Determine molecular formula from line or condensed structure.
Reactions of Hydrocarbons
Halogenation: Replacement of hydrogen with a halogen (e.g., Cl, Br).
Identify possible products when given a reactant and reaction conditions.
Know the three positions for disubstituted benzenes: ortho (1,2-), meta (1,3-), para (1,4-).
Appendix: Key Equations and Constants
Avogadro's number: (atoms, molecules, or ions)
Molarity (M):
Dilution:
Equilibrium constant:
Water dissociation:
pH:
pK_a:
Henderson-Hasselbalch:
Appendix: Periodic Table
The periodic table organizes elements by increasing atomic number and groups elements with similar chemical properties. It is essential for determining atomic masses, valence electrons, and predicting chemical behavior.
Additional info: The study guide covers foundational GOB Chemistry topics, including chemical reactions, stoichiometry, acids and bases, equilibrium, and introductory organic chemistry. The included tables and equations are essential for problem-solving and conceptual understanding in a GOB Chemistry course.