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STOP – Before you click submit, check that you have answered…

STOP – Before you click submit, check that you have answered all the questions. Check at the top of the screen that all your questions have a check mark. If not, click on the ones that have a (?) to go back and answer the question. Questions√Question 1 (?) Question 2

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What is the correct IUPAC name for the following structure?…

What is the correct IUPAC name for the following structure?    

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What configurations are found in the product(s) of the react…

What configurations are found in the product(s) of the reaction below?

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Which of the following alkenes is most stable? Write your an…

Which of the following alkenes is most stable? Write your answer using a number in the text box below. 

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Which of the following alkenes is most stable? Write your an…

Which of the following alkenes is most stable? Write your answer using a number in the text box below.  

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What reagents are necessary to complete the following transf…

What reagents are necessary to complete the following transformation?    

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Classify the following molecule as and E isomer, a Z isomer,…

Classify the following molecule as and E isomer, a Z isomer, or neither. Write your answer in the text box below using capital letters. 

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What is the major organic product formed in the following re…

What is the major organic product formed in the following reaction?

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A reaction of an unknown alkene with meta-chloroperoxybenzoi…

A reaction of an unknown alkene with meta-chloroperoxybenzoic acid (MCPBA) in dichloromethane followed by hydrolysis with H2O/H+ yielded, as the major product, a racemic mixture of (2S, 3S) and (2R, 3R)-3-methylpentan-2,3-diol. What is the specific structure of the alkene used in the reaction?

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Which of the following does characterize a more highly subst…

Which of the following does characterize a more highly substituted carbocation? I.  Forms more rapidly than less highly substituted carbocationsII. Forms product more slowly than less highly substituted carbocationsIII. Has a smaller ΔGŧ (activation energy) than less highly substituted carbocationsIV. Is more stable than less highly substituted carbocations  

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