1. Z-2-chlorocyclopentanol and E-2-chlorocyclopentanol eachreact with NaOH to eliminate HCl but they give different finalproducts C5H8O. Show how each forms
2. The reactions of bromotrichloromethane with toluene in thepresence of a peroxide affords trichloromethane and benzyl bromide.Show the mechanism, indicating the chain carrying and initiatingsteps
3.
Show how to convert 2-hydroxypropane to 1-hydroxypropane:
(a) Using BH3 at some point
(b) Not using BH3
4.
Show the products of the reaction of Br2 with cis-2-butnene (Z)and with trans-2-butene (E). Show and them any enantiomersformed.
(a) in pentane (b) in water, forming bromoalcohols
