Homework 5 1st

Homework 5 1st - Take Assessment: Homework 5 Homework 5...

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Take Assessment: 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 Save Consider the following two stereoisomers. How are they different?
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Question 1 5 points Save Question 2 5 points Save Which of the following statements is(are) true for the compound cis-1,2- dichlorocyclopr opane?
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Question 2 5 points Save Question 3 5 points Save Below is the structure of cholesterol. What is the maximum number of optically active stereoisomers for the cholesterol molecule?
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Question 4 5 points Save The molecule shown below is chiral. Question 5 5 points Save Which of the following statements is (are) true for the compound (3R,4R)-3,4- dimethylhexane ?
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Question 5 5 points Save Question 6 5 points Save Determine the relationship between the two molecules shown. Question 7 5 points Save An optically active compound is composed of 75% of the (R) enantiomer and 25% of the (S) enantiomer. The enantiomeric
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Question 7 5 points Save excess (ee) is equal to Question 8 5 points Save What is the specific rotation ([α] D ) of the following molecule?
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Question 9 5 points Save If a sample of 2-butanol has an enantiomeric excess of 60% of l -2-butanol, how much of each isomer is present? Question 10 5 points Save How many stereocenters are there in the following molecule?
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5 points Save Question 11 5 points Save The molecule shown below can be described as a meso compound. Question 12
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This note was uploaded on 02/22/2011 for the course CHEM 301 taught by Professor Norris during the Spring '11 term at FSU.

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Homework 5 1st - Take Assessment: Homework 5 Homework 5...

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