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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

Test 2:Stereocenter Test

R and S Configuration

Enantiomers vs. Diastereomers

Atropisomers

Meso Compound

Test 3:Disubstituted Cycloalkanes

What is the Relationship Between Isomers?

Fischer Projection

R and S of Fischer Projections

Optical Activity

Enantiomeric Excess

Calculations with Enantiomeric Percentages

Non-Carbon Chiral Centers

Energy Diagram

Gibbs Free Energy

Enthalpy

Entropy

Hammond Postulate

Carbocation Stability

Carbocation Intermediate Rearrangements

Nucleophilic Substitution

Good Leaving Groups

SN2 Reaction

SN1 Reaction

Substitution Comparison

Organic Chemistry 1 Midterm - Part 3 of 3

In the given reaction, if the temperature is increased, which side of the reaction, if any, would be favored?