Exam 4: Isomers: the Arrangement of Atoms in Space
Exam 1: Remembering General Chemistry: Electronic Structure and Bonding90 Questions
Exam 2: Acids and Bases: Central to Understanding Organic Chemistry43 Questions
Exam 3: An Introduction to Organic Compounds: Nomenclature, physical Properties, and Structure136 Questions
Exam 4: Isomers: the Arrangement of Atoms in Space125 Questions
Exam 5: Alkenes: Structure,nomenclature,and an Introduction to Reactivity - Thermodynamics and Kinetics84 Questions
Exam 6: The Reactions of Alkenes - the Stereochemistry of Addition Reactions89 Questions
Exam 7: The Reactions of Alkynes - Introduction to Multistep Synthesis124 Questions
Exam 8: Delocalized Electrons: Their Effect on Stability, pka, and the Products of a Reaction - Aromaticity and Electronic Effects: an Introduction to the Reactions of Benzene185 Questions
Exam 9: Substitution and Elimination Reactions of Alkyl Halides228 Questions
Exam 10: Reactions of Alcohols, ethers, epoxides, amines and Sulfur-Containing Compounds109 Questions
Exam 11: Organometallic Compounds65 Questions
Exam 12: Radicals141 Questions
Exam 13: Mass Spectrometry,infrared Spectroscopy,and Uvvis Spectroscopy140 Questions
Exam 14: Nmr Spectroscopy122 Questions
Exam 15: Reactions of Carboxylic Acids and Carboxylic Acid Derivatives126 Questions
Exam 16: Reactions of Aldehydes and Ketones122 Questions
Exam 17: Reactions at the Α-Carbon121 Questions
Exam 18: Reactions of Benzene and Substituted Benzenes168 Questions
Exam 19: More About Amines - Reactions of Heterocylic Compounds126 Questions
Exam 20: The Organic Chemistry of Carbohydrates110 Questions
Exam 21: Amino Acids,peptides,and Proteins117 Questions
Exam 22: Catalysis in Organic Reactions and in Enzymatic Reactions92 Questions
Exam 23: The Organic Chemistry of the Coenzymes, compounds Derived From Vitamins102 Questions
Exam 24: The Organic Chemistry of the Metabolic Pathways90 Questions
Exam 25: The Organic Chemistry of Lipids37 Questions
Exam 26: The Chemistry of the Nucleic Acids94 Questions
Exam 27: Synthetic Polymers116 Questions
Exam 28: Pericyclic Reactions102 Questions
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Which of the following terms best describes the pair of compounds shown: enantiomers,diastereomers,or the same compound? 

(Short Answer)
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(-)-Mandelic acid has a specific rotation of -158°.What would be the specific rotation of a solution which contains 40% (-)-mandelic acid and 60% (+)-mandelic acid?
(Multiple Choice)
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Which of the following terms best describes the pair of compounds shown: enantiomers,diastereomers,or the same compound? 

(Short Answer)
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Can one predict whether a compound with a single asymmetric center is dextro- or levorotatory based on the R/S assignment at this asymmetric center? Explain briefly.
(Essay)
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Draw a enantiomer of the α-pinene present in juniper berry that is used to flavor gin. 

(Essay)
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Determine the E/Z and R,S configuration for 7,8-dihydrovomifoliol which is responsible for the fruity aroma of champagne. 

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How many stereoisomers exist with the following basic connectivity? CH3CHClCH2CHClCH3
(Multiple Choice)
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What is the relationship between the structures shown below? 

(Multiple Choice)
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Which of the following terms best describes the pair of compounds shown: enantiomers,diastereomers,or the same compound? 

(Short Answer)
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The configuration of R-(+)-glyceraldehyde is as follows:
What is the absolute configuration of (-)-lactic acid? 


(Multiple Choice)
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Which of the following terms best describes the pair of compounds shown: enantiomers,diastereomers,or the same compound? 

(Short Answer)
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Assign an R or S configurational label to each asymmetric center in the molecule below. 

(Essay)
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Consider the molecules with molecular formula C2H2Br2Cl2.
(a)Draw a structure that is optically inactive because it does not have an asymmetric center.
(b)Draw a structure that is optically inactive because it is a meso compound.
(c)Draw a structure that is optically active because it is chiral.
(Essay)
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A solution containing 0.96 g of 2-bromooctane in 10 mL ether solution gave an observed rotation of -1.8° in a 10 cm cell at 20°C.Calculate the specific rotation of this solution.
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