Exam 8: Alcohols, Phenols, Ethers, and Their Sulfur Analogs
Exam 1: Structure and Bonding:acids and Bases41 Questions
Exam 2: Alkanes: the Nature of Organic Compounds44 Questions
Exam 3: Alkenes and Alkynes: the Nature of Organic Reactions40 Questions
Exam 4: Reactions of Alkenes and Alkynes44 Questions
Exam 5: Aromatic Compounds52 Questions
Exam 6: Sterechemistry at Tetrahedral Centers39 Questions
Exam 7: Organohalides: Nucleophilic Substitutions and Eliminations40 Questions
Exam 8: Alcohols, Phenols, Ethers, and Their Sulfur Analogs36 Questions
Exam 9: Aldehydes and Ketones: Nucleophilic Addition Reactions32 Questions
Exam 10: Carboxylic Acids and Derivatives: Nucleophilic Acyl Substitution Reactions63 Questions
Exam 11: Carbonyl Alpha-Substitution Reactions and Condensation Reactions38 Questions
Exam 12: Amines32 Questions
Exam 13: Structure Determination65 Questions
Exam 14: Biomolecules: Carbohydrates48 Questions
Exam 15: Biomolecules: Amino Acids, Peptides, and Proteins50 Questions
Exam 16: Biomolecules: Lipids and Nucleic Acids50 Questions
Exam 17: The Organic Chemistry of Metabolic Pathways40 Questions
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Instructions: Consider the Grignard reaction below to answer the following question(s).
-Refer to instructions. The nucleophile in this reaction is indicated by letter _____.
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(Short Answer)
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Correct Answer:
A
Instructions: Draw structures corresponding to each of the following IUPAC names.
-Draw:
cyclopropyl ethyl sulfide
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(Essay)
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Correct Answer:

A useful and general method for the synthesis of alcohols is the addition of Grignard reagents to carbonyl compounds. Show what Grignard reagent and what carbonyl compound you would start with to prepare each alcohol below. List all possibilities. 
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Correct Answer:

Instructions:
Give the major organic product(s) of the following reactions or sequences of reactions. Show all relevant stereochemistry.
-Write the product(s): 
(Essay)
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Instructions: Consider the Grignard reaction below to answer the following question(s).
-Refer to instructions. The electrophile in this reaction is indicated by letter _____.
(Short Answer)
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Instructions:
Give the major organic product(s) of the following reactions or sequences of reactions. Show all relevant stereochemistry.
-Write the product(s): 
(Essay)
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Instructions: Draw structures corresponding to each of the following IUPAC names.
-Draw:
2-phenylpropan-2-ol
(Essay)
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Instructions: Draw structures corresponding to each of the following IUPAC names.
-Draw:
Dicyclohexyl sulfide
(Essay)
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Instructions: Provide correct IUPAC names for each of the structures below.
-Name: 
(Short Answer)
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Instructions: Consider the reaction below to answer the following question.
-Refer to instructions. On the structures provided below draw arrows showing the mechanism of step two of this reaction. 
(Essay)
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Instructions: Draw structures corresponding to each of the following IUPAC names.
-Draw:
3-methylbut-2-en-1-ol
(Essay)
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Instructions:
Give the major organic product(s) of the following reactions or sequences of reactions. Show all relevant stereochemistry.
-Write the product(s): 
(Essay)
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Instructions: To answer the following question(s), consider the reaction below.
-Refer to instructions. On the templates provided below, draw both conformations of the alcohol product. Circle the least stable conformation. 
(Essay)
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Instructions:
Give the major organic product(s) of the following reactions or sequences of reactions. Show all relevant stereochemistry.
-Write the product(s): 
(Essay)
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Instructions:
Give the major organic product(s) of the following reactions or sequences of reactions. Show all relevant stereochemistry.
-Write the product(s): 
(Essay)
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Choose the best reagent for carrying out the following reactions from the list below. Place the letter of the reagent(s) in the box over the reaction arrow. Only one letter per box.
A)m-ClC6H4CO3H
B)H2/Pd
C)warm H2SO4/H2O
D)PCC, CH2Cl2
E)LiAlH4 in ether, then H3O+
F)NaOH, heat
(Essay)
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Instructions: Draw structures corresponding to each of the following IUPAC names.
-Draw:
2, 4, 6-trinitrophenol
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