Exam 18: Aromatic Substitution Reactions
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
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Exam 27: Synthetic Polymers119 Questions
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Provide the reagents necessary to carry out the following conversion. 

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Propose a stepwise synthesis for the following compound from benzene. 

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Provide the reagents necessary to carry out the following conversion. 

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A nitro group ___________ the benzene ring to make it __________ reactive than benzene.
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Cyclohexene undergoes an addition reaction with bromine, but benzene does not. Instead, benzene undergoes a substitution reaction with bromine. Explain why.
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Which one of the following compounds will be most reactive towards an electrophilic aromatic bromination reaction?
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Provide the structures of the intermediate products and final product in the following reaction sequence. 

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Provide the reagents necessary to prepare 1-bromo-3-isobutylbenzene from benzene.
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Provide the reagents necessary to carry out the following conversion. 

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Identify the electrophile for the Friedel-Crafts acylation of benzene.
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Draw the major resonance contributors for the intermediate that results when p-chloronitrobenzene is treated with NaOH.
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Which of the following substituents will direct the incoming group to the ortho/para position during electrophilic aromatic substitution?
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Arrange the following compounds in order of decreasing reactivity towards electrophilic aromatic substitution. 

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Which of the following substituents will not direct the incoming group to the ortho/para position during electrophilic aromatic substitution?
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Provide the reagents necessary to carry out the following conversion. 

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