CHEM 110
McGill
Course Overview
Grade Boosters
Lessons & Practice
I. Welcome
1 min1. Quantum Theory and Atomic Structure
4hr2. Electron Configuration and Chemical Periodicity
4hr3. Models of Chemical Bonding
2.3hr4. The Shapes of Molecules
1.1hr5. Theories of Covalent Bonding
54min5.2.1. Molecular Orbital Theory Introduction3 min5.2.2. How to Draw MO Diagrams for Homonuclear Diatomics8 min5.2.3. Example: Molecular Orbitals of Li2 min5.2.4. Example: Molecular Orbitals of HeH3 min5.2.5. Practice: Diamagnetic Diatomics2 min5.2.6. Practice: MO Orbitals2 min5.2.7. Practice: Molecular Orbital (Challenging Problem)
6. Intermolecular Forces
1.9hr7. Organic Compounds
1.1hr7.3.1. Naming Simple Hydrocarbons4 min7.3.2. Hydrocarbon Example2 min7.3.3. Practice: Hydrocarbon Naming7.3.4. Practice: Hydrocarbon Naming 27.3.5. Steps to Naming Complex Organic Molecules4 min7.3.6. Naming Organic Molecules with Odd Functional Groups2 min7.3.7. Nomenclature Practice7.3.8. Practice: Naming Problem 27.3.9. Practice: Naming Problem 3
7.4.1. Conformational Isomers7.4.2. Newman Projections3 min7.4.3. Rotomers of 2-methylbutane2 min7.4.4. Newman Projection Conversion Concept Clarifier7.4.5. Anti vs Gauche Interactions3 min7.4.6. Ranking the Energy of Rotomoers Practice Question #27.4.7. Drawing Most Stable Rotomer Practice Question7.4.8. Cyclohexane Rings3 min7.4.9. Chair Flip Practice7.4.10. 1,3-diaxial Interactions in Cyclohexane Rings2 min7.4.11. Energy of Chair Structures Practice Question
7.5.1. Confirmations and Stereochemistry Introduction1 min7.5.2. E vs Z4 min7.5.3. Example: Which Molecules have Cis and Trans Isomers3 min7.5.4. Concept Clarifier7.5.5. Practice: Naming Alkenes with Stereochemistry1 min7.5.6. Chirality5 min7.5.7. Optical Isomers, R vs S6 min7.5.8. Asymmetric Centers Example7.5.9. Practice: Molecules which display chirality2 min7.5.10. Practice: Assigning Stereocenters7.5.11. Practice: Assigning Stereocenters7.5.12. Unrelated vs Diastereomers vs Enantiomers vs Identical5 min7.5.13. Stereoisomer practice problems7.5.14. Isomer Summary
8. Intro to Reactions
55min8.1.1. General Types of Organic Reactions2 min8.1.2. Nucleophiles and Electrophiles1 min8.1.3. Nucleophilic Substitution Reactions3 min8.1.4. Concept Clarifier8.1.5. SN2 Product Prediction Concept Clarifier8.1.6. Elimination Reactions2 min8.1.7. Addition to Alkenes and alkynes3 min8.1.8. Markovnikov's Rule1 min8.1.9. Predict the Products Alkene Addition8.1.10. Alkene Addition Practice Problem8.1.11. Practice: Bromine Addition Problem8.1.12. Addition Polymerization4 min8.1.13. Example: Converting a Monomer to a Polymer2 min8.1.14. Polymer Formation Questions8.1.15. Practice: Monomer Identification8.1.16. Practice: Polymer Identification
8.2.1. Periodic Trends Summary Sheet8.2.2. General Trends in p-block Bonding3 min8.2.3. Oxidation States Theory3 min8.2.4. Example: Oxidation States in the Hydroxide Ion32 sec8.2.5. Oxidation State Practice Questions8.2.6. Practice: Oxidation State of Sulphur in Sulphate and Sulphite1 min8.2.7. Practice: Oxidation State of Carbon in Methane21 sec
9. Transition Elements and Their Coordination Compounds
31min9.1.1. Complexes and ligands8 min9.1.2. Writing Chemical Formulas of Transition Metal Complexes5 min9.1.3. Isomers3 min9.1.4. Stereoisomers6 min9.1.5. Transition Metal Complexes Practice Question9.1.6. Practice: Isomers9.1.7. Practice: Isomers II9.1.8. Practice: Transition Metal Shapes9.1.9. Practice: Transition Metal Complexes9.1.10. Stereochemistry of Transition Metals Summary
9.2.1. Crystal Field Theory4 min9.2.2. Color of Transition Metal Complexes2 min9.2.3. Steps to Understanding Transition Metal Complex Colours2 min9.2.4. Paramagnetism and High-Spin/Low-Spin Complexes2 min9.2.5. Practice: Transition Metal Complex Absoprtion9.2.6. Practice: Transition Metal Complex Colours9.2.7. Practice: High Spin vs Low Spin
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