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Chris Sorensen

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Chris Sorensen & Ammul Shergill

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Lost in reaction mechanisms, functional groups, or synthesis problems? Organic chemistry becomes manageable through step-by-step guidance and practice.

Johnny Betancourt

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Jules Bruno

1. A Review of General Chemistry

2. Molecular Representations

3. Acids and Bases

4. Alkanes and Cycloalkanes

5. Chirality

6. Thermodynamics and Kinetics

7. Substitution Reactions

8. Elimination Reactions

9. Alkenes and Alkynes

10. Addition Reactions

11. Radical Reactions

12. Alcohols, Ethers, Epoxides and Thiols

13. Alcohols and Carbonyl Compounds

14. Synthetic Techniques

15. Analytical Techniques:IR, NMR, Mass Spect

16. Conjugated Systems

17. Ultraviolet Spectroscopy

18. Aromaticity

19. Reactions of Aromatics: EAS and Beyond

20. Phenols

21. Aldehydes and Ketones: Nucleophilic Addition

22. Carboxylic Acid Derivatives: NAS

23. The Chemistry of Thioesters, Phophate Ester and Phosphate Anhydrides

24. Enolate Chemistry: Reactions at the Alpha-Carbon

25. Condensation Chemistry

26. Amines

27. Heterocycles

28. Carbohydrates

29. Amino Acids

30. Peptides and Proteins

31. Catalysis in Organic Reactions

32. Lipids 

33. The Organic Chemistry of Metabolic Pathways

34. Nucleic Acids

35. Transition Metals

36. Synthetic Polymers

[BOOK ORGO] CLUTCH

Ernest

Leaving Group Conversions - Sulfonyl Chlorides

Leaving Group Conversions Summary

Williamson Ether Synthesis

Making Ethers - Alkoxymercuration

Making Ethers - Alcohol Condensation

Making Ethers - Acid-Catalyzed Alkoxylation

Making Ethers - Cumulative Practice

Ether Cleavage

Alcohol Protecting Groups

Silyl Ether Protecting Groups

Sharpless Epoxidation

Thiol Reactions

Sulfide Oxidation

Oxidizing and Reducing Agents

Reducing Agent

Nucleophilic Addition

Preparation of Organometallics

Grignard Reaction

Protecting Alcohols from Organometallics

Organometallic Cumulative Practice

Moving Functionality

Alkynide Alkylation

Alkane Halogenation

Retrosynthesis

Organic Chemistry 1 Final - Part 3 of 3

What are the electrophile and the nucleophile in the first step of the reaction mechanism?