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CHEM 1121: General, Organic, and Biochemistry
- Publisher
- LibreTexts
- Source
- LibreTexts
- Language
- EN
- Category
- Basic Sciences
Contents· 175 sections
- 01: Measuring Matter and Energy
- 1.01: What is Chemistry
- 1.02: Classification of Matter
- 1.03: Introduction to Kinetic and Potential Energy
- 1.04: Measurements
- 1.05: Expressing Numbers- Scientific Notation
- 1.06: Expressing Numbers- Significant Figures
- 1.07: The International System of Units
- 1.08: Converting Units
- 1.09: Temperature Conversions
- 1.10: Specific Heat
- 1.11: Dosage Calculations
- 1.12: Chapter Summary
- 02: Atomic Structure
- 2.01: The Elements
- 2.02: Atomic Theory
- 2.03: The Structure of Atoms
- 2.04: Nuclei of Atoms
- 2.05: Arrangement of Electron (Shell Model)
- 2.06: The Periodic Table
- 2.07: Chapter Summary
- 03: Nuclear Chemistry
- 3.01: Radioactivity
- 3.02: Half-Life
- 3.03: Units of Radioactivity
- 3.04: Uses of Radioactive Isotopes
- 3.05: Nuclear Energy
- 3.06: 3.6 Chapter Summary
- 3.07: Ionic Bonding and Simple Ionic Compounds
- 04: Ionic Bonding and Simple Ionic Compounds
- 4.01: Two Types of Bonding
- 4.02: Ions
- 4.03: Formulas for Ionic Compounds
- 4.04: Ionic Nomenclature
- 4.05: Chapter Summary
- 05: Covalent Bonding and Simple Molecular Compounds
- 5.01: Covalent Bonds
- 5.02: Covalent Compounds- Formulas and Names
- 5.03: Multiple Covalent Bonds
- 5.04: Characteristics of Covalent Bonds
- 5.05: Characteristics of Molecules
- 5.06: Intermolecular Forces
- 5.07: Chapter Summary
- 06: Introduction to Chemical Reactions
- 6.01: Prelude to Introduction to Chemical Reactions
- 6.02: The Law of Conservation of Matter
- 6.03: Chemical Equations
- 6.04: Quantitative Relationships Based on Chemical Equations
- 6.05: Types of Chemical Reactions
- 6.06: Oxidation-Reduction (Redox) Reactions
- 6.07: Redox Reactions in Organic Chemistry and Biochemistry
- 6.E: Introduction to Chemical Reactions (Exercises)
- 6.S: Introduction to Chemical Reactions (Summary)
- 07: Quantities in Chemical Reactions
- 7.01: Formula Mass
- 7.02: The Mole
- 7.03: Atomic and Molar Masses
- 7.04: Mole-Mass Conversions
- 7.05: Mole-Mole Relationships in Chemical Reactions
- 7.06: Energetics of Biochemical Reactions
- 7.07: Factors Affecting Reaction Rates
- 7.08: Catalysis
- 7.09: Equilbria and Le Chatelier's Principle
- 7.10: Chapter Summary
- 08: States of Matter and the Gas Laws
- 8.01: Phase Changes
- 8.02: Solids Liquids and Gases
- 8.03: Gases and Pressure
- 8.04: Gas Laws
- 8.05: Chapter Summary
- 09: Solutions
- 9.01: Introduction to Solutions
- 9.02: Solution Concentration- Molarity
- 9.03: Other Units for Solution Concentrations
- 9.04: The Dissolution Process
- 9.05: Properties of Solutions
- 9.06: Dialysis and Tonicity
- 9.07: Chapter Summary
- 10: Acids and Bases
- 10.01: Arrhenius Definition of Acids and Bases
- 10.02: Brnsted-Lowry Definition of Acids and Bases
- 10.03: Water is both an Acid and a Base
- 10.04: The Strengths of Acids and Bases
- 10.05: pH and Kw
- 10.06: Buffers
- 10.07: End-of-Chapter Material
- 11: Organic Chemistry of Hydrocarbons
- 11.01: Introduction to Organic Chemistry
- 11.02: Organic Chemistry
- 11.03: Structures and Names of Alkanes
- 11.04: Branched-Chain Alkanes
- 11.05: Condensed Structural and Line-Angle Formulas
- 11.06: Cycloalkanes
- 11.07: IUPAC Nomenclature
- 11.08: Alkenes- Structure and Nomenclature
- 11.09: Alkenes- Cis-Tran Isomerization
- 11.10: Alkynes
- 11.11: Aromatic Compounds
- 11.12: Aromatic Compounds- Structure and Nomenclature
- 11.13: Physical Properties of Hydrocarbons
- 11.14: Chapter Summary
- 12: Organic Functional Groups - Structure and Nomenclature
- 12.01: Organic Compounds with Functional Groups
- 12.02: 9.2 Alcohols and Phenols- Nomenclature and Classification
- 12.03: Glycols and Glycerol
- 12.04: Ethers
- 12.05: Aldehydes and Ketones- Structure and Names
- 12.06: Organic Sulfur Compounds
- 12.07: Carboxylic Acids- Structures and Names
- 12.08: Esters- Structures and Names
- 12.09: Phosphate Esters
- 12.10: Amines
- 12.11: Amides
- 13: Organic Reactions
- 13.01: Organic Reactions
- 13.02: Organic Reactions (Exercises)
- 14: Properties of Organic Functional Groups
- 14.01: Physical Properties of Alcohols
- 14.02: Physical Properties of Aldehydes and Ketones
- 14.03: Physical Properties of Carboxylic Acids
- 14.04: Physical Properties of Esters
- 14.05: Physical Properties of Amines
- 14.06: Physical Properties of Amides
- 14.07: Ionization of Carboxylic Acids
- 14.08: Amines as Bases
- 14.09: Chirality
- 14.10: End-of-Chapter Material
- 15: Carbohydrates
- 15.01: Introduction to Carbohydrates
- 15.02: Classes of Monosaccharides
- 15.03: Important Hexoses
- 15.04: Cyclic Structures of Monosaccharides
- 15.05: Properties of Monosaccharides
- 15.06: Disaccharides
- 15.07: Polysaccharides
- 15.08: Diabetes
- 15.09: Chapter Summary
- 16: Lipids
- 16.01: Introduction to Lipids
- 16.02: Fatty Acids
- 16.03: Fats and Oils
- 16.04: Membranes and Membrane Lipids
- 16.05: Steroids
- 16.06: Chapter Summary
- 17: Proteins and Enzymes
- 17.01: Properties of Amino Acids
- 17.02: Reactions of Amino Acids
- 17.03: Peptides
- 17.04: Proteins
- 17.05: Enzymes
- 17.06: Enzymatic Catalysis
- 17.07: Enzymatic Activity
- 17.08: Enzyme Inhibition
- 17.09: Enzyme Cofactors and Vitamins
- 17.10: Chapter Summary
- 18: Nucleic Acids
- 18.01: Nucleotides
- 18.02: Nucleic Acid Structure
- 18.03: Replication and Expression of Genetic Information
- 18.04: Protein Synthesis and the Genetic Code
- 18.05: Mutations and Genetic Diseases
- 18.06: Viruses
- 18.07: Chapter Summary
- 19: Energy Metabolism
- 19.01: Prelude to Energy Metabolism
- 19.02: ATP- the Universal Energy Currency
- 19.03: Stage I of Catabolism
- 19.04: Overview of Stage II of Catabolism
- 19.05: Stage III of Catabolism
- 19.06: Stage II of Carbohydrate Catabolism
- 19.07: Stage II of Lipid Catabolism
- 19.08: Stage II of Protein Catabolism
- 19.09: Oxidative Phosphorylation
- 19.10: Energy Metabolism (Exercises)
- 19.11: Energy Metabolism (Summary)