a. Give the structure of the products obtained from the reaction of each enantiomer of cis-1 chloro-2-isopropylcyclopentane
Question:
a high concentration of sodium methoxide in methanol.
b. Are all the products optically active?
c. How would the products differ if the starting material were the trans isomer? Are all these products optically active?
d. Will the cis enantiomers or the trans enantiomers form substitution products more rapidly?
e. Will the cis enantiomers or the trans enantiomers form elimination products more rapidly?
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a These are S N 2E2 reactions b Only the substitution products ar...View the full answer
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