Exam 17: Aromatic Compounds
Exam 1: A Review of General Chemistry: Electrons, Bonds, and Molecular Properties191 Questions
Exam 2: Molecular Representations168 Questions
Exam 3: Acids and Bases127 Questions
Exam 4: Alkanes and Cycloalkanes116 Questions
Exam 5: Stereoisomerism141 Questions
Exam 6: Chemical Reactivity and Mechanisms96 Questions
Exam 7: Alkyl Halides: Nucleophilic Substitution and Elimination Reactions224 Questions
Exam 8: Addition Reactions of Alkenes153 Questions
Exam 9: Alkynes177 Questions
Exam 10: Radical Reactions102 Questions
Exam 11: Synthesis106 Questions
Exam 12: Alcohols and Phenols147 Questions
Exam 13: Ethers and Epoxides; Thiols and Sulfides139 Questions
Exam 14: Infrared Spectroscopy and Mass Spectrometry135 Questions
Exam 15: Nuclear Magnetic Resonance Spectroscopy140 Questions
Exam 16: Conjugated Pi Systems and Pericyclic Reactions140 Questions
Exam 17: Aromatic Compounds118 Questions
Exam 18: Aromatic Substitution Reactions122 Questions
Exam 19: Aldehydes and Ketones169 Questions
Exam 20: Carboxylic Acids and Their Derivatives144 Questions
Exam 21: Alpha Carbon Chemistry: Enols and Enolates147 Questions
Exam 22: Amines112 Questions
Exam 23: Introduction to Organometallic Compounds118 Questions
Exam 24: Carbohydrates144 Questions
Exam 25: Amino Acids, Peptides, and Proteins133 Questions
Exam 26: Lipids123 Questions
Exam 27: Synthetic Polymers119 Questions
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Provide the structure of the major product(s) for the following reaction. 
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Provide the reagents necessary to carry out the following conversion. 
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Provide the structures of the intermediates and final product in the following reaction sequence. 
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Provide the structure of the major product(s) for the following reaction.

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Classify the following compound as aromatic, antiaromatic, or nonaromatic. Explain your choice. 
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Which one of the following statements is not true for a compound to be considered as aromatic?
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Classify the following compound as aromatic, antiaromatic, or nonaromatic. Explain your choice. 
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Identify the aromatic hydrocarbon with the highest stabilization energy per ring.
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Which one of the following compounds would exhibit seven signals in its 13C NMR spectrum? 
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Provide the reagents necessary to carry out the following conversion. 
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Provide a structure for the compound with molecular formula C10H12O2 and with the following spectroscopic data.
IR: 1680 cm−1, 2750 cm−1, 2850 cm−1
1H NMR: 1.1 (triplet, 3H), 3.5 (quartet, 2H), 4.5 (singlet, 2H), 7.3 (doublet, 2H), 7.7 (doublet, 2H), 9.9 (singlet, 1H)
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Using a Frost circle, draw the molecular orbital energy diagram for the cyclononatetraenyl cation and predict if it is aromatic. 
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