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

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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

Infrared Spectroscopy

Infrared Spectroscopy Table

IR Spect:Drawing Spectra

NMR Spectroscopy

1H NMR:Number of Signals

1H NMR:Q-Test

1H NMR:E/Z Diastereoisomerism

H NMR Table

1H NMR:Spin-Splitting (N + 1) Rule

1H NMR:Spin-Splitting Simple Tree Diagrams

1H NMR:Spin-Splitting Complex Tree Diagrams

1H NMR:Spin-Splitting Patterns

NMR Integration

NMR Practice

Carbon NMR

Structure Determination without Mass Spect

Mass Spectrometry

Mass Spect:Fragmentation

Mass Spect:Isotopes

Aromaticity

Huckel's Rule

Pi Electrons

Aromatic Hydrocarbons

Annulene

Aromatic Heterocycles

Frost Circle

Naming Benzene Rings

Acidity of Aromatic Hydrocarbons

Organic Chemistry 2 Midterm - Part 1 of 4

Determine if each of the following statements is true or false:i. The coupling constant in hertz (Hz) is directly proportional to the operating frequency.ii. Compared to the operating frequency in IR and UV-vis spectroscopy, the operating frequency in NMR spectroscopy is much higher.

Determine if each of the following statements is true or false:

i. The coupling constant in hertz (Hz) is directly proportional to the operating frequency.
ii. Compared to the operating frequency in IR and UV-vis spectroscopy, the operating frequency in NMR spectroscopy is much higher.