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  3. 1. z-2-chlorocyclopentanol and e-2-chlorocyclopent

1. Z-2-chlorocyclopentanol and E-2-chlorocyclopentanol each react with NaOH to eliminate HCl but they give different final products...

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Chemistry

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

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