A)I,ii and iii please a) The alkene drawn here undergoes an electrophilic addition reaction with HBr.5i) Give the IUPAC name of this molecule.ii) Outline the mechanism of this reaction. Your mechanism should show the formation ofBOTH possible products and should also name both products.iii) Explain why the Markovnikov rule does not predict a major product in this case.b) The common name of the molecule drawn below is diisopropyl ether. Its structural formulais (CH3)2CHOH(CH3)2.totIt can be synthesized in two steps using the starting materials propan-2-ol, 2-chloropropaneand sodium metal. One of these steps is a nucleophilic substitution reaction.i) Using structural formulae, write two balanced chemical equations representing the two stepsof this synthesis. No state symbols are required.ii) Outline the mechanism of the nucleophilic substitution step.

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Answered: A)I,ii and iii please

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A)I,ii and iii please

Organic Chemistry

8th Edition

ISBN:9781305580350

Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Publisher:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Chapter8: Haloalkanes, Halogenation, And Radical Reactions

Section: Chapter Questions

Problem 8.21P

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Question

A)I,ii and iii please

a) The alkene drawn here undergoes an electrophilic addition reaction with HBr.
5
i) Give the IUPAC name of this molecule.
ii) Outline the mechanism of this reaction. Your mechanism should show the formation of
BOTH possible products and should also name both products.
iii) Explain why the Markovnikov rule does not predict a major product in this case.
b) The common name of the molecule drawn below is diisopropyl ether. Its structural formula
is (CH3)2CHOH(CH3)2.
tot
It can be synthesized in two steps using the starting materials propan-2-ol, 2-chloropropane
and sodium metal. One of these steps is a nucleophilic substitution reaction.
i) Using structural formulae, write two balanced chemical equations representing the two steps
of this synthesis. No state symbols are required.
ii) Outline the mechanism of the nucleophilic substitution step.

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