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When an alkene is subjected to treatment with Hg(OAc)2 in methanol followed by reaction with NaBH4, what new class of compound is formed?

In the following ozonolysis reaction, if we start with optically pure S-enantiomer, the product(s) obtained will be  

For the following problem, use a separate sheet of paper for your answers and then upload your answers at the following link:   https://canvas.dccc.edu/courses/28473/assignments/571797   Your work must be shown for full credit.   1. Provide the major organic product(s) for each of the following reactions. Show any relevant stereochemistry.  a.           b.          c.            d.          e.    

Which of the following isomers is the most stable alkene? Write your answer in the text box below.                 A                          B                                    C                                   D

Which of the following alkenes reacts with HCl at the slowest rate? A.   B.           C..   D.    E.                                                                                                                                                                                                                                            

What reagents are necessary to cause the following transformation?                                       —————–>                 

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

What is the correct IUPAC name for the following compound?  

How many elements of unsaturation do molecules with a molecular formula of C6H6Cl6 have?

What alkene, which contains no oxygen atoms and a single C=C, will give CH3CO(CH2)4CHO upon treatment with OsO4 followed by cleavage with periodic acid?