Freshman Organic Chemistry with J. Michael McBride
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What you'll learn
This course includes
- 30 hours of video
- Certificate of completion
- Access on mobile and TV
Course content
1 modules • 37 lessons • 30 hours of video
Freshman Organic Chemistry with J. Michael McBride
37 lessons
• 30 hours
Freshman Organic Chemistry with J. Michael McBride
37 lessons
• 30 hours
- 1. How Do You Know? 46:41
- 2. Force Laws, Lewis Structures and Resonance 50:13
- 3. Double Minima, Earnshaw's Theorem and Plum-Puddings 45:03
- 4. Coping with Smallness and Scanning Probe Microscopy 50:02
- 5. X-Ray Diffraction 47:10
- 6. Seeing Bonds by Electron Difference Density 51:10
- 7. Quantum Mechanical Kinetic Energy 49:18
- 8. One-Dimensional Wave Functions 49:51
- 9. Chladni Figures and One-Electron Atoms 49:36
- 10. Reality and the Orbital Approximation 48:34
- 11. Orbital Correction and Plum-Pudding Molecules 49:27
- 12. Overlap and Atom-Pair Bonds 50:35
- 13. Overlap and Energy-Match 49:44
- 14. Checking Hybridization Theory with XH_3 47:36
- 15. Chemical Reactivity: SOMO, HOMO, and LUMO 47:12
- 16. Recognizing Functional Groups 50:08
- 17. Reaction Analogies and Carbonyl Reactivity 41:44
- 18. Amide, Carboxylic Acid and Alkyl Lithium 51:21
- 19. Oxygen and the Chemical Revolution (Beginning to 1789) 47:10
- 20. Rise of the Atomic Theory (1790-1805) 50:01
- 21. Berzelius to Liebig and Wöhler (1805-1832) 49:22
- 22. Radical and Type Theories (1832-1850) 49:15
- 23. Valence Theory and Constitutional Structure (1858) 48:47
- 24. Determining Chemical Structure by Isomer Counting (1869) 50:15
- 25. Models in 3D Space (1869-1877); Optical Isomers 49:02
- 26. Van't Hoff's Tetrahedral Carbon and Chirality 48:27
- 27. Communicating Molecular Structure in Diagrams and Words 51:36
- 28. Stereochemical Nomenclature; Racemization and Resolution 47:30
- 29. Preparing Single Enantiomers and the Mechanism of Optical Rotation 50:19
- 30. Esomeprazole as an Example of Drug Testing and Usage 50:43
- 31. Preparing Single Enantiomers and Conformational Energy 48:53
- 32. Stereotopicity and Baeyer Strain Theory 46:18
- 33. Conformational Energy and Molecular Mechanics 47:53
- 34. Sharpless Oxidation Catalysts and the Conformation of Cycloalkanes 49:18
- 35. Understanding Molecular Structure and Energy through Standard Bonds 48:42
- 36. Bond Energies, the Boltzmann Factor and Entropy 47:51
- 37. Potential Energy Surfaces, Transition State Theory and Reaction Mechanism 47:44
