Exam 5: Stereoisomerism
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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Draw the Fischer projection of the following compound. 
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Drawn below is the structure of Plavix (clopidogrel), a medication used to manage blood clots. Assign the absolute configuration of the chirality center as R or S. 
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S
Which of the following is the correct IUPAC name of the following structure? SHAPE \* MERGEFORMAT

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B
Drawn below is the structure of Singulair (montelukast), a medication used to manage athsma. Assign the absolute configuration of the chirality center as R or S. 
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What is the specific rotation of a sample of carvone that is an equal mixture of the R and S enantiomers? (R)- carvone has a specific rotation of −61.
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Redraw the structure below as a wedge-dash structure and label any/all stereocenters with their absolute configuration. 
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The structure of Crestor (rosuvastatin), a medication used to reduce cholesterol, is shown below. If the specific rotation for this compound is known to be +100, what would be the specific rotation for the stereoisomer shown at the right? 
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Which of the following structures is a correct wedge/dash drawing of the following Fischer projection?

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Assign the absolute configuration of the chirality center as R or S. 
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