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Home » Basic and Health Sciences » Chemistry » Freshman Organic Chemistry I (Yale) » 28. Stereochemical Nomenclature; Racemization and Resolution (Yale)

28. Stereochemical Nomenclature; Racemization and Resolution (Yale)

Course:Freshman Organic Chemistry I (Yale)
Discipline:Basic and Health Sciences
Institute:Yale University
Instructor(s): Professor J. Michael McBride
Level:College

Freshman Organic Chemistry I (Yale)

1. How Do You Know? (Yale)
10. Reality and the Orbital Approximation (Yale)
11. Orbital Correction and Plum-Pudding Molecules (Yale)
12. Overlap and Atom-Pair Bonds (Yale)
13. Overlap and Energy-Match (Yale)
14. Checking Hybridization Theory with XH_3 (Yale)
15. Chemical Reactivity: SOMO, HOMO, and LUMO (Yale)
16. Recognizing Functional Groups (Yale)
17. Reaction Analogies and Carbonyl Reactivity (Yale)
18. Amide, Carboxylic Acid and Alkyl Lithium (Yale)
19. Oxygen and the Chemical Revolution (Beginning to 1789) (Yale)
2. Force Laws, Lewis Structures and Resonance (Yale)
20. Rise of the Atomic Theory (1790-1805) (Yale)
21. Berzelius to Liebig and Wöhler (1805-1832) (Yale)
22. Radical and Type Theories (1832-1850) (Yale)
23. Valence Theory and Constitutional Structure (1858) (Yale)
25. Models in 3D Space (1869-1877); Optical Isomers (Yale)
24. Determining Chemical Structure by Isomer Counting (1869) (Yale)
32. Stereotopicity and Baeyer Strain Theory (Yale)
33. Conformational Energy and Molecular Mechanics (Yale)

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