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Arianne Dee

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Mariya Breyther

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Chris Sorensen

Data Analysis Fundamentals with Excel

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Chris Sorensen & Ammul Shergill

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George Levy

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Lee Donahoe & Michael Hartl

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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

Carbene

Epoxidation

Epoxide Reactions

Dihydroxylation

Ozonolysis

Ozonolysis Full Mechanism

Oxidative Cleavage

Alkyne Oxidative Cleavage

Alkyne Hydrohalogenation

Alkyne Halogenation

Alkyne Hydration

Alkyne Hydroboration

Radical Reaction

Radical Stability

Free Radical Halogenation

Radical Selectivity

Calculating Radical Yields

Anti Markovnikov Addition of Br

Allylic Bromination

Radical Synthesis

Alcohol Nomenclature

Naming Ethers

Naming Epoxides

Naming Thiols

Alcohol Synthesis

Leaving Group Conversions - Using HX

Leaving Group Conversions - SOCl2 and PBr3

Organic Chemistry 1 Final - Part 2 of 3

Draw the structure consistent with the name 3,4-epoxy-2-methylheptane.