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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

Basicity of Aromatic Heterocycles

Ionization of Aromatics

Electrophilic Aromatic Substitution

Benzene Reactions

EAS:Halogenation Mechanism

EAS:Nitration Mechanism

EAS:Friedel-Crafts Alkylation Mechanism

EAS:Friedel-Crafts Acylation Mechanism

EAS:Any Carbocation Mechanism

Electron Withdrawing Groups

Acylation of Aniline

Limitations of Friedel-Crafts Alkyation

Blocking Groups - Sulfonic Acid

EAS:Synergistic and Competitive Groups

Side-Chain Halogenation

Side-Chain Oxidation

Birch Reduction

EAS:Sequence Groups

EAS:Retrosynthesis

Diazo Replacement Reactions

Diazo Sequence Groups

Diazo Retrosynthesis

Nucleophilic Aromatic Substitution

Benzyne

Naming Aldehydes

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Oxidizing and Reducing Agents

Organic Chemistry 2 Midterm - Part 2 of 4

Name the carbonyl-containing compound below. If possible, provide both common and IUPAC names.CH2(Cl)CH2CH2CH2CH(CH3)CHO

Name the carbonyl-containing compound below. If possible, provide both common and IUPAC names.
CH₂(Cl)CH₂CH₂CH₂CH(CH₃)CHO