Exam 5: Aromatic Compounds
Exam 1: Structure and Bonding:acids and Bases40 Questions
Exam 2: Alkanes: The Nature of Organic Compounds47 Questions
Exam 3: Alkenes and Alkynes: the Nature of Organic Reactions37 Questions
Exam 4: Reactions of Alkenes and Alkynes44 Questions
Exam 5: Aromatic Compounds51 Questions
Exam 6: Sterechemistry at Tetrahedral Centers35 Questions
Exam 7: Organohalides: Nucleophilic Substitutions and Eliminations49 Questions
Exam 8: Alcohols, Phenols, Ethers, and Their Sulfur Analogs39 Questions
Exam 9: Aldehydes and Ketones: Nucleophilic Addition Reactions32 Questions
Exam 10: Carboxylic Acids and Derivatives: Nucleophilic Acyl Substitution Reactions66 Questions
Exam 11: Carbonyl Alpha-Substitution Reactions and Condensation Reactions37 Questions
Exam 12: Amines31 Questions
Exam 13: Structure Determination64 Questions
Exam 14: Biomolecules: Carbohydrates41 Questions
Exam 15: Biomolecules: Amino Acids, Peptides, and Proteins43 Questions
Exam 16: Biomolecules: Lipids and Nucleic Acids37 Questions
Exam 17: The Organic Chemistry of Metabolic Pathways35 Questions
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Instructions:
Given the major organic product(s) of each of the following reactions. If no reaction is predicted, write "N.R."
Write the product: 
Free
(Essay)
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Correct Answer:

Instructions: Provide the IUPAC name for each of the following compounds.
IUPAC Name:
Free
(Essay)
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Correct Answer:
m-nitrotoluene
What is the major organic product obtained from the following reaction? 
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(Multiple Choice)
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Correct Answer:
C
Instructions: Consider the reaction below to answer the following question(s).
Refer to instructions. This reaction proceeds _____________ (faster or slower) than benzene.
(Short Answer)
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Which of the following sets of substituents are all o/p-directing in electrophilic aromatic substitution reactions?
(Multiple Choice)
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Instructions: Consider the reaction below to answer the following question(s).
Refer to instructions. Draw the structure of product
D.
(Essay)
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Instructions:
Consider the Friedel-Crafts alkylation reaction below to answer the following questions:
What is the role of the AlCl3 in the reaction?
(Essay)
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Consider the production of 1-bromo-4-nitrobenzene:
a) Explain why Pathway A for the production of 1-bromo-4-nitrobenzene produces a higher yield of the product.
b) If reaction Pathway A is carried out at high temperatures, a trisubstituted product forms. Draw the structure of the product and explain why it forms.
(Essay)
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Instructions:
Given the major organic product(s) of each of the following reactions. If no reaction is predicted, write "N.R."
Write the product:
(Essay)
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What is the correct assignment of the names of the following aromatic compounds? 
(Multiple Choice)
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Instructions: Consider the reaction below to answer the following question(s).
Refer to instructions. The nucleophile in the reaction is indicated by letter _____.
(Short Answer)
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Circle the compound(s) in the following set that will undergo both substitution and addition when treated with Br2. 
(Essay)
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Which of the following undergoes the most rapid acylation upon treatment with acetyl chloride and AlCl3?
(Multiple Choice)
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Instructions: Consider the reaction below to answer the following question(s).
Refer to instructions. The Lewis acid catalyst in the reaction is indicated by letter _____.
(Short Answer)
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