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25 Pages

Homework 5 1st

Course: CHEM 301, Spring 2011
School: FSU
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Word Count: 976

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Assessment: Take Homework 5 Homework 5 Select the best answer. This Test allows 5 attempts. This is attempt number 1. This Test can be saved and resumed later. Question Completion Status: 1 2 3 4 5 21 22 23 24 25 Question 1 5 points Consider the following two stereoisomers. How are they different? Save Question 1 5 points Save Question 2 5 points Which of the following statements is(are) true...

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Assessment: Take Homework 5 Homework 5 Select the best answer. This Test allows 5 attempts. This is attempt number 1. This Test can be saved and resumed later. Question Completion Status: 1 2 3 4 5 21 22 23 24 25 Question 1 5 points Consider the following two stereoisomers. How are they different? Save Question 1 5 points Save Question 2 5 points Which of the following statements is(are) true for the compound cis-1,2dichlorocyclopr opane? Save Question 2 5 points Save Question 3 5 points Below is the structure of cholesterol. What is the maximum number of optically active stereoisomers for the cholesterol molecule? Save Question 4 5 points The molecule shown below is chiral. Save Question 5 5 points Which of the following statements is (are) true for the compound (3R,4R)-3,4dimethylhexane ? Save Question 5 5 points Save Question 6 5 points Determine the relationship between the two molecules shown. Save Question 7 5 points An optically active compound is composed of 75% of the (R) enantiomer and 25% of the (S) enantiomer. The enantiomeric Save Question 7 5 points excess (ee) is equal to Save Question 8 5 points What is the specific rotation ([]D) of the following molecule? Save Question 9 5 points If a sample of 2-butanol has an enantiomeric excess of 60% of l-2-butanol, how much of each isomer is present? Save Question 10 5 points How many stereocenters are there in the following molecule? Save Question 10 5 points Save Question 11 5 points The molecule shown below can be described as a meso compound. Save Question 12 5 points Which of the statements below correctly describes an achiral molecule? Save Question 12 5 points Save Question 13 5 points The molecule shown below is chiral. Save Question 14 5 points Which of the 7 isomers of Save Question 14 5 points cichlorocyclohe xane possess a plane of symmetry? Save Question 15 5 points Which of the following may be separated by ordinary physical methods? Save Question 16 5 points Carvone has Save Question 16 5 points two stereo isomers that are shown below. (+)-carvone smells like caraway seed and (-)-carvone has a spearmint odor. What direction does (=)-carvone rotate plane polarized light? Save Question 17 5 points In the assignment of absoloute Save Question 17 5 points configuration of molecule I below, what priority does the ethyl group have? Save Question 18 5 points The molecule shown below is chiral. Save Question 19 5 points Carvone has two stereo isomers that are shown below. (+)-carvone smells like caraway seed and (-)-carvone has a spearmint odor. What physical properties will be different for (+)-carvone and (-)-carvone? Save I. Density II. Boiling point III. Rotation of plane polarized light Question 20 5 points The molecule shown below is chiral. Save Question 21 5 points Give the sterochemical relationships between the two compounds shown below. Save Question 21 5 points Save Question 22 5 points How many stereoisomers are possible for 1-ethyl-3methylcyclohex ane? Save Question 23 5 points Give the sterochemical relationships between the two compounds shown below. Save Question 23 5 points Save Question 24 5 points Below is the structure of cholesterol. How many chiral centers are present in cholesterol? Save Question 25 5 points Which of the following has a plane of symmetry? Save Review Assessment: Homework 5 Christopher Lee Kelbaugh 10/16/10 2:09 Homework AM 5 Completed 95 out of 125 points Select the best answer. Question 1 5 out of 5 points Consider the following two stereoisomers. How are they different? Selected Answer: Question 2 0 out of 5 points Which of the following statements is(are) true for the compound cis-1,2dichlorocyclopropane? Selected Answer: Question 3 5 out of 5 points Below is the structure of cholesterol. What is the maximum number of optically active stereoisomers for the cholesterol molecule? Selected Answer: Question 4 The molecule shown below is chiral. 0 out of 5 points Selected Answer: Question 5 0 out of 5 points Which of the following statements is (are) true for the compound (3R,4R)-3,4dimethylhexane? Selected Answer: Question 6 Determine the relationship between the two molecules shown. 5 out of 5 points Selected Answer: Question 7 5 out of 5 points An optically active compound is composed of 75% of the (R) enantiomer and 25% of the (S) enantiomer. The enantiomeric excess (ee) is equal to Selected Answer: Question 8 What is the specific rotation ([]D) of the following molecule? 5 out of 5 points Question 8 Selected Answer: 5 out of 5 points Question 9 5 out of 5 points If a sample of 2-butanol has an enantiomeric excess of 60% of l-2-butanol, how much of each isomer is present? Selected Answer: Question 10 How many stereocenters are there in the following molecule? 5 out of 5 points Selected Answer: Question 11 5 out of 5 points The molecule shown below can be described as a meso compound. Selected Answer: Question 12 Selected Answer: 5 out of 5 points Which of the statements below correctly describes an achiral molecule? Question 13 The molecule shown below is chiral. 5 out of 5 points Selected Answer: Question 14 Selected Answer: 5 out of 5 points Which of the 7 isomers of cichlorocyclohexane possess a plane of symmetry? Question 15 Selected Answer: 5 out of 5 points Which of the following may be separated by ordinary physical methods? Question 16 5 out of 5 points Carvone has two stereo isomers that are shown below. (+)-carvone smells like caraway seed and (-)-carvone has a spearmint odor. What direction does (=)carvone rotate plane polarized light? Selected Answer: Question 17 5 out of 5 points In the assignment of absoloute configuration of molecule I below, what priority does the ethyl group have? Selected Answer: Question 18 The molecule shown below is chiral. 5 out of 5 points Selected Answer: Question 19 0 out of 5 points Carvone has two stereo isomers that are shown below. (+)-carvone smells like caraway seed and (-)-carvone has a spearmint odor. What physical properties will be different for (+)-carvone and (-)-carvone? I. Density II. Boiling point III. Rotation of plane polarized light Selected Answer: Question 20 The molecule shown below is chiral. 5 out of 5 points Selected Answer: Question 21 0 out of 5 points Give the sterochemical relationships between the two compounds shown below. Selected Answer: Question 22 Selected Answer: 5 out of 5 points How many stereoisomers are possible for 1-ethyl-3-methylcyclohexane? Question 23 0 out of 5 points Give the sterochemical relationships between the two compounds shown below. Selected Answer: Question 24 5 out of 5 points Below is the structure of cholesterol. How many chiral centers are present in cholesterol? Selected Answer: Question 25 Which of the following has a plane of symmetry? Selected Answer: 5 out of 5 points
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