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CHEM 2213
UWO
Course Overview
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Lessons & Practice
1. Anatomy of an Organic Molecule
1.6hr2. Organic Molecules as Acid-Base Reactions
56min2.2.1. Factors Influencing Acid/Base Strength2 min2.2.2. Electronegativity1 min2.2.3. Atom Size2 min2.2.4. Resonance3 min2.2.5. Hybridization3 min2.2.6. Induction3 min2.2.7. Aromaticity3 min2.2.8. Example: Acid/Base Strength 3 min2.2.9. Example: Acid/Base Strength 3 min2.2.10. Practice: Acid/Base Equilibria 2 min2.2.11. Practice: Acid/Base Equilibria 2 min
2.3.1. Important pKas You Should Know4 min2.3.2. Relationship Between pH and pKa2 min2.3.3. Amino Acids at Different pHs3 min2.3.4. Practice: Amino Acids in Solution3 min2.3.5. Practice: Amino Acids in Solution3 min2.3.6. Summary Sheet: Amino Acids in Solution of Various pH2.3.7. Summary Sheet: pKa's of Common Molecules
3. Fundamentals of Organic Structure: Molecular Conformations (Alkanes and Cycloalkanes)
50min3.5.1. IUPAC Systematic Naming Theory15 min3.5.2. Example: Converting Names to Structures2 min3.5.3. Example: IUPAC Systematic Naming2 min3.5.4. Example: IUPAC Systematic Naming2 min3.5.5. Practice: IUPAC Systematic Naming2 min3.5.6. Practice: IUPAC Systematic Naming2 min3.5.7. Summary Sheet: IUPAC Naming
4. Isomerism and Stereochemistry
1.5hr5. Alkyl Halides and Nucleophilic Substitutions and Eliminations
1.4hr6. Addition Reactions of Alkenes
2.2hr7. Aromaticity and Electrophilic Aromatic Substitution
48min8. Alcohols and Phenols Reactivity
59min8.3.1. SN1/SN2 Reactions of Alkyl Halides (Review)8.3.2. Electrophilic Addition to Alkenes: Acid-catalyzed Hydration (Review)8.3.3. Electrophilic Addition to Alkenes: Hydroboration/Oxidation (Review)8.3.4. Electrophilic Addition to Alkenes: Dihydroxylation (Review)8.3.5. Nomenclature and Physical Properties of Aldehydes and Ketones (Brief Introduction)8.3.6. General Reactivity of Aldehydes and Ketones (Brief Introduction)1 min8.3.7. General Mechanism at the Carbonyl4 min8.3.8. Reduction of Aldehydes and Ketones using NaBH42 min8.3.9. Reduction of any Carbonyl using LiAlH44 min8.3.10. Example: Reduction Reactions3 min8.3.11. Example: Reductions Reactions5 min8.3.12. The Grignard Reaction5 min8.3.13. Example: The Grignard Reaction2 min8.3.14. Practice: The Grignard Reaction5 min8.3.15. Study Sheet: Reaction Overview and Key Ideas
9. Structure Elucidation: IR, 13C-NMR, 1H-NMR
1.9hr10. Chemistry of Aldehydes and Ketones
2.3hr10.7.1. General Reactions with Oxygen Nucleophiles5 min10.7.2. Hydrate Formation1 min10.7.3. Acetal Formation2 min10.7.4. Ketal Formation2 min10.7.5. Hydrolysis of Acetals and Ketals3 min10.7.6. General Mechanism with Oxygen Nucleophiles9 min10.7.7. Stability of Hemiketals and Hemiacetals3 min10.7.8. Practice: Ketals and Acetals as Protecting Groups2 min10.7.9. Practice: Ketals and Acetals as Protecting Groups2 min10.7.10. Example: Synthesis and Hydrolysis of Ketals and Acetals1 min10.7.11. Practice: Mechanism in Acetal and Ketal Formation3 min10.7.12. Practice: Reagents in Acetal and Ketal Chemistry10.7.13. Practice: Identifying Acetals/Aldehydes2 min
10.9.1. Tautomerization8 min10.9.2. Enolate Formation3 min10.9.3. Kinetic vs. Thermodynamic Enolates5 min10.9.4. The Aldol Reaction3 min10.9.5. Mechanism of the Aldol Reaction5 min10.9.6. The Retro-Aldol Reaction1 min10.9.7. Mixed Aldol Reactions5 min10.9.8. Example: The Aldol Reaction4 min10.9.9. Practice: The Aldol Reaction2 min
11. Carboxylic Acids and Derivatives
1.1hrCHEM 2213 Overview
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Welcome to CHEM 2213! This on-demand course was put together especially for CHEM 2213 at UWO. Use the video lessons and notes to understand your lecture topics better, and the practice questions to cement your knowledge. And don't hesitate to leave a question in the Q&A box under each lesson if you need additional help with anything. Happy studying!
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Course Notes
Wizeprep's course notes with hundreds of easy-to-understand explanations, diagrams, and practice problems.