Exam 7: Alkenes and Alkynes
Exam 1: Structure and Bonding30 Questions
Exam 2: Polar Covalent Bonds: Acids and Bases35 Questions
Exam 3: Organic Compounds: Alkanes and Their Stereochemistry32 Questions
Exam 4: Organic Compounds: Cycloalkanes and Their Stereochemistry18 Questions
Exam 5: Stereochemistry at Tetrahedral Centers33 Questions
Exam 6: An Overview of Organic Reactions32 Questions
Exam 7: Alkenes and Alkynes34 Questions
Exam 8: Reactions of Alkenes and Alkynes37 Questions
Exam 9: Aromatic Compounds36 Questions
Exam 10: Structure Determination: Mass Spectrometry,infrared Spectroscopy,and Ultraviolet Spectroscopy41 Questions
Exam 11: Structure Determination: Nuclear Magnetic Resonance Spectroscopy37 Questions
Exam 12: Organohalides: Nucleophilic Substitutions and Eliminations37 Questions
Exam 13: Alcohols,phenols,and Thiols: Ethers and Sulfides19 Questions
Exam 14: Aldehydes and Ketones: Nucleophilic Addition Reactions30 Questions
Exam 15: Carboxylic Acids and Nitriles23 Questions
Exam 16: Carboxylic Acid Derivatives: Nucleophilic Acyl Substitution Reactions42 Questions
Exam 17: Carbonyl Alpha-Substitution and Condensation Reactions84 Questions
Exam 18: Amines and Heterocycles28 Questions
Exam 19: Biomolecules: Amino Acids,peptides,and Proteins36 Questions
Exam 20: Amino Acid Metabolism34 Questions
Exam 21: Biomolecules: Carbohydrates42 Questions
Exam 22: Carbohydrate Metabolism41 Questions
Exam 23: Biomolecules: Lipids and Their Metabolism31 Questions
Exam 24: Biomolecules: Nucleic Acids and Their Metabolism23 Questions
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Rank each set of substituents using the Cahn-Ingold-Prelog sequence rules by numbering the highest priority substituent 1 and numbering the lowest priority substituent 4.Place the number in the blank below the substituent.
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Draw structures corresponding to each name below.
-Draw:
trans-4,4-dimethylpent-2-ene
(Essay)
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Below are all the chemical structures and intermediates involved in a reaction.On the structures provided,show all electron flow using the arrow formalism for the complete stepwise mechanism.
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Instructions: Dieldrin,C12H8Cl6O,is a pentacyclic (five-ring)compound formerly used as an insecticide.Use this information to answer the following question(s).
-Refer to instructions.Calculate the degree of unsaturation for Dieldrin.
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A compound with the following molecular formula contains two double bonds.What is the correct subscript for H in the formula?
C10H?ClN2O
(Multiple Choice)
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Rank the carbocations below in order of increasing stability (least stable = 1;most stable = 3).Place the number corresponding to the carbocation's relative stability in the blank below the structure.
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Instructions: Provide names for each structure below.Be sure to include the cis,trans or E,Z designations where applicable.
Name and designate:
(Essay)
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Instructions: Assign E or Z configurations to each alkene below.
Assign:
(Essay)
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Choose substituents X and Y (listed in order below)for the following compound so as to make a Z isomer. 
(Multiple Choice)
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