Chapter 3, Problem 137EQ

Give the major organic product of the following reaction sequence.

Provide the curved-arrow mechanism to account for the following nucleophillic addition-elimination reaction.

One of the two diastereomers shown below reacts with potassium tertbutoxide significantly faster than then the other. Which one is it? Provide an explanation and predict the product of the fast reaction.

Explain why compound A will not undergo a ring-opening reaction under thermal conditions, but compound B will.

Please complete both subpart reactions in clear handwritten answer on a paper!

Kepone, aldrin, and chlordane are synthesized from hexachlorocyclopentadiene and other five-membered-ring compounds. Show how these three pesticides are composed of two five-membered rings.

If toluene and vinyl chloride have Friedel -  Crafts alkylation, what major product will be?

Give a clear handwritten answer with explanation..give the  SN2 mechanism of given bleow reaction

Give the major products