Oregon Institute of Technology
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- OIT: CHE 101 - Introductory Chemistry
- OIT: CHE 201 - General Chemistry I (Clark)
- Unit 1: The Scale of the Atomic World
- Unit 2: The Structure of the Atom
- Unit 3: Nuclei, Ions, and Molecules
- 3.1: Nuclear Chemistry and Radioactive Decay
- 3.1: Nuclear Chemistry and Radioactive Decay (Problems)
- 3.2: A Brief History of the Organization of the Periodic Table
- 3.2: A Brief History of the Organization of the Periodic Table (Problems)
- 3.3: Writing Chemical Formulas
- 3.3: Writing Chemical Formulas (Problems)
- 3.4: Molecular and Ionic Compounds
- 3.4: Molecular and Ionic Compounds (Problems)
- Unit 4: Quantifying Chemicals
- Unit 5: Transformations of Matter
- Unit 6: Common Chemical Reactions
- 6.1: Calculating Molarity
- 6.1: Calculating Molarity (Problems)
- 6.2: Solutions Chemistry
- 6.2: Solutions Chemistry (Problems)
- 6.3: Classifying Chemical Reactions (Precipitation)
- 6.3: Classifying Chemical Reactions (Precipitation) (Problems)
- 6.4: Classifying Chemical Reactions (Acids and Bases)
- 6.4: Classifying Chemical Reactions (Acids and Bases) (Problems)
- 6.5: Classifying Chemical Reactions (Redox)
- 6.5: Classifying Chemical Reactions (Redox) (Problems)
- Unit 7: Ideal Gas Behavior
- 7.1: Temperature and Pressure
- 7.1: Temperature and Pressure (Problems)
- 7.2: The Gas Laws
- 7.2: The Gas Laws (Problems)
- 7.3: Applications of the Ideal Gas Law and Partial Pressures
- 7.3: Applications of the Ideal Gas Law and Partial Pressures (Problems)
- 7.4: Kinetic Molecular Theory
- 7.4: Kinetic Molecular Theory (Problems)
- Unit 8: Thermochemistry
- OIT: CHE 202 - General Chemistry II (Clark)
- Unit 1: The Quantum World
- Unit 2: Electrons in Atoms
- Unit 3: Periodic Patterns
- Unit 4: Lewis Structures
- Unit 5: Molecular Shape
- Unit 6: Molecular Polarity
- Unit 7: Intermolecular Forces in Action
- Unit 8: Solutions and Phase Changes
- Unit 9: Semiconductors
- OIT: CHE 315 - Environmental Chemistry & Toxicology (Clark)
- OIT: CHE 331 - Organic Chemistry (Under construction)
- AGENDA (Fall)
- Sample Agenda: Organic Chemistry
- Text
- Introduction to Organic Chemistry (Soderberg)
- Week 1: Gen chem recap, and O-chem intro
- Week 1: General chemistry recap & Organic chemistry intro
- 2: Introduction to Organic Structure and Bonding II
- Introduction
- Homework
- Labs
- OIT: CHE 332 -- Organic Chemistry II (Lund)
- 1: Fall term review chapters
- 1: Chapter 3 - Conformations and Stereochemistry
- 1.1: Conformations of open-chain organic molecules
- 1.2: Conformations of cyclic organic molecules
- 1.3: Chirality and stereoisomers
- 1.4: the R and S system
- 1.5: Optical Activity
- 1.6: Compounds with multiple chiral centers
- 1.7: Meso compounds
- 1.8: Fischer and Haworth projections
- 1.9: Stereochemistry in biology and medicine
- 1.10: Prochirality
- 1.11: Stereochemistry of alkenes
- 1.12: Problems for Chapter 3
- 1.13: Solutions to Chapter 3 exercises
- 2: Chapter 6 - Overview of Organic Reactivity
- 2.1: Prelude to Organic Reactivity
- 2.2: A First Look at Some Organic Reaction Mechanism
- 2.3: A Quick Review of Thermodynamics and Kinetics
- 2.4: Catalysis
- 2.5: Comparing Biological Reactions to Laboratory Reactions
- 2.6: Overview of Organic Reactivity (Exercises)
- 2.7: Overview of Organic Reactivity (Summary)
- 1: Chapter 3 - Conformations and Stereochemistry
- 7: Acid-base Reactions
- 1: Prelude to Acid-base Reactions
- 2: Overview of Acid-Base Reactions
- 3: The Acidity Constant
- 4: Structural Effects on Acidity and Basicity
- 5: Acid-base Properties of Phenols
- 6: Acid-base properties of nitrogen-containing functional groups
- 7: Carbon Acids
- 8: Polyprotic Acids
- 9: Effects of enzyme microenvironment on acidity and basicity
- 10: Acid-base Reactions (Exercises)
- 11: Acid-base Reactions (Summary)
- 8: Nucleophilic Substitution Reactions
- 1: Prelude to Nucleophilic Substitution Reactions
- 2: Two Mechanistic Models for Nucleophilic Substitution
- 3: Nucleophiles
- 4: Electrophiles
- 5: Leaving Groups
- 6: Regiochemistry of SN1 Reactions with Allylic Electrophiles
- 7: SN1 or SN2? Predicting the Mechanism
- 8: Biological Nucleophilic Substitution Reactions
- 9: Nucleophilic substitution in the Lab
- 10: Nucleophilic Substitution Reactions (Exercises)
- 11: Nucleophilic Substitution Reactions (Summary)
- 9: Phosphate Transfer Reactions
- 1: Prelude to Phosphate Transfer Reactions
- 2: Overview of Phosphate Groups
- 3: Phosphate Transfer Reactions - An Overview
- 4: ATP, The Principal Phosphate Group Donor
- 5: Phosphorylation of Alcohols
- 6: Phosphorylation of Carboxylates
- 7: Hydrolysis of Organic Phosphates
- 8: Phosphate Diesters in DNA and RNA
- 9: The Organic Chemistry of Genetic Engineering
- 10: NMR of phosphorylated compounds
- 11: Phosphate Transfer Reactions (Exercise)
- 12: Phosphate Transfer Reactions (Summary)
- 10: Nucleophilic Carbonyl Addition Reactions
- 1: Prelude to Nucleophilic Carbonyl Addition Reactions
- 2: Nucleophilic Additions to Aldehydes and Ketones - An Overview
- 3: Hemiacetals, Hemiketals, and Hydrates
- 4: Acetals and Ketals
- 5: N-glycosidic Bonds
- 6: Imines
- 7: A Look Ahead - Addition of Carbon and Hydride Nucleophiles to Carbonyls
- 8: Nucleophilic Carbonyl Addition Reactions (Exercises)
- 9: Nucleophilic Carbonyl Addition Reactions (Summary)
- 11: Nucleophilic Acyl Substitution Reactions
- 1: Prelude to Nucleophilic Acyl Substitution Reactions
- 2: Carboxylic Acid Derivatives
- 3: The Nucleophilic Acyl Substitution Mechanism
- 4: The Relative Reactivity of Carboxylic Acid Derivatives
- 5: Acyl Phosphates
- 6: Acyl Phosphates
- 7: Hydrolysis of Thioesters, Esters, and Amides
- 8: Protein Synthesis on the Ribosome
- 9: Nucleophilic Substitution at Activated Amides and Carbamides
- 10: Nucleophilic Acyl Substitution Reactions in the Laboratory
- 11: A Look Ahead - Acyl Substitution Reactions with a Carbanion or Hydride Ion Nucleophile
- 12: Nucleophilic Acyl Substitution Reactions (Exercises)
- 13: Nucleophilic Acyl Substitution Reactions (Summary)
- 12: Reactions at the α-Carbon, Part I
- 1: Prelude to Reactions at the α-carbon, part I
- 2: Review of Acidity at the α-Carbon
- 3: Isomerization at the α-Carbon
- 4: Aldol Addition
- 5: α-Carbon Reactions in the Synthesis Lab - Kinetic vs. Thermodynamic Alkylation Products
- 6: Reactions at the α-Carbon, Part I (Exercises)
- 7: Reactions at the α-Carbon, Part I (Summary)
- 1: Fall term review chapters
- OIT: CHE 333 - Organic Chemistry III (sample)
- 1: Spring Term Agenda
- 2: Text
- 13 - Reactions at the α-Carbon, Part II
- 14 - Electrophilic Reactions
- 15 - Oxidation and Reduction Reactions
- Flavin-Dependent Monooxygenase Reactions - Hydroxylation, Epoxidation, and the Baeyer-Villiger Oxidation
- Hydrogenation of alkenes and Dehydrogenation of Alkanes
- Hydrogenation of Carbonyl and Imine Groups
- Hydrogen Peroxide is a Harmful - Reactive Oxygen Species
- Monitoring Hydrogenation and Dehydrogenation Reactions by UV Spectroscopy
- Oxidation and Reduction in the Context of Metabolism
- Oxidation and Reduction of Organic Compounds - An Overview
- Oxidation and Reduction Reactions (Summary)
- Oxidation and Reduction Reactions (Exercises)
- Prelude to Oxidation and Reduction Reactions
- Redox Reactions of Thiols and Disulfides
- 16 - Radical Reactions
- Destruction of the Ozone Layer by a Radical Chain Reaction
- Flavin as a One-Electron Carrier
- Overview of Single-Electron Reactions and Free Radicals
- Oxidative Damage to cells, Vitamin C, and Scurvy
- Prelude to Radical Reactions
- Radical Chain Reactions
- Radical Reactions (Exercises)
- Radical Reactions (Summary)
- Useful Polymers formed by Radical Chain Reactions
- 17 - The Organic Chemistry of Vitamins
- Labs
- Practice Problems
- OIT: CHE 333 -- Organic Chemistry III (Lund)
- 1: Reactions at the α-Carbon, Part II
- 2: Retrosynthetic analysis and metabolic pathway prediction
- 3: Electrophilic Reactions
- 4: Oxidation and Reduction Reactions
- 4.1: Prelude to Oxidation and Reduction Reactions
- 4.2: Oxidation and Reduction of Organic Compounds - An Overview
- 4.3: Oxidation and Reduction in the Context of Metabolism
- 4.4: Hydrogenation of Carbonyl and Imine Groups
- 4.5: Hydrogenation of alkenes and Dehydrogenation of Alkanes
- 4.6: Monitoring Hydrogenation and Dehydrogenation Reactions by UV Spectroscopy
- 4.7: Redox Reactions of Thiols and Disulfides
- 4.8: Flavin-Dependent Monooxygenase Reactions - Hydroxylation, Epoxidation, and the Baeyer-Villiger Oxidation
- 4.9: Hydrogen Peroxide is a Harmful - Reactive Oxygen Species
- 4.10: Oxidation and Reduction Reactions (Exercises)
- 4.11: Oxidation and Reduction Reactions (Summary)
- 5: Radical Reactions
- 5.1: Prelude to Radical Reactions
- 5.2: Overview of Single-Electron Reactions and Free Radicals
- 5.3: Radical Chain Reactions
- 5.4: Useful Polymers formed by Radical Chain Reactions
- 5.5: Destruction of the Ozone Layer by a Radical Chain Reaction
- 5.6: Oxidative Damage to cells, Vitamin C, and Scurvy
- 5.7: Flavin as a One-Electron Carrier
- 5.8: Radical Reactions (Exercises)
- 5.9: Radical Reactions (Summary)
- 6: The Organic Chemistry of Vitamins
- 6.1: Prelude to the Organic Chemistry of Vitamins
- 6.2: Pyridoxal Phosphate (Vitamin B6)
- 6.3: Thiamine Diphosphate (Vitamin B1)
- 6.4: Thiamine Diphosphate, Lipoamide and the Pyruvate Dehydrogenase Reaction
- 6.5: Folate
- 6.6: The Oganic Chemistry of Vitamins (Exercises)
- 6.7: The Oganic Chemistry of Vitamins (Summary)
- 7: Index of enzymatic reactions by pathway
- 8: Index of laboratory synthesis reactions
OIT: CHE 101 - Introductory Chemistry
OIT: CHE 201 - General Chemistry I (Clark)
OIT: CHE 202 - General Chemistry II (Clark)
OIT: CHE 315 - Environmental Chemistry & Toxicology (Clark)
OIT: CHE 331 - Organic Chemistry (Under construction)
OIT: CHE 332 -- Organic Chemistry II (Lund)
OIT: CHE 333 - Organic Chemistry III (sample)
OIT: CHE 333 -- Organic Chemistry III (Lund)