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Learn the toughest concepts covered in Organic Chemistry with step-by-step video tutorials and practice problems by world-class tutors.

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Johnny Betancourt

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

E2 Mechanism

E2 - Anti-Coplanar Requirement

E2 - Cumulative Practice

E1 Reaction

Solvents

Leaving Groups

Nucleophiles and Basicity

SN1 SN2 E1 E2 Chart (Big Daddy Flowchart)

Cumulative Substitution/Elimination

Alkene Stability

Zaitsev Rule

Dehydrohalogenation

Double Elimination

Acetylide

Hydrogenation of Alkynes

POCl3 Dehydration

Alkynide Synthesis

Addition Reaction

Markovnikov

Hydrohalogenation

Acid-Catalyzed Hydration

Oxymercuration

Hydroboration

Hydrogenation

Halogenation

Organic Chemistry 1 Final - Part 1 of 3

The reaction shown below involves a step where the hydroxy group in the reactant is converted to a good leaving group via protonation. Propose a reasonable mechanism for the reaction.