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Chapter 6: Q47P (page 275)

a. What products will be obtained from the addition of Br2 to cyclohexene if H2O is added to the reaction

mixture?

b. Propose a mechanism for the reaction.

Short Answer

Expert verified

Double bond will attack on bromine atom and one bromine ion will release and another bromine ion will make bond with both carbon atoms which form double bond and with the addition of bromine it converts into single bond. Now oxygen lone pair of water molecule will attack on carbon which is bonded with bromine ion it can attack on either of the carbon and two substituents will form by releasing H+ ion.

Step by step solution

01

How reaction proceed

Double bond will attack on bromine atom and one bromine ion will release and another bromine ion will make bond with both carbon atoms which form double bond and with the addition of bromine it converts into single bond. Now oxygen lone pair of water molecule will attack on carbon which is bonded with bromine ion it can attack on either of the carbon and two substituents will form by releasing H+ ion.

02

Final answer

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Most popular questions from this chapter

When fumarate reacts with D2O in the presence of the enzyme fumarase, only one isomer of the product is formed, as shown here. Is the enzyme catalyzing a syn or an anti-addition of D2O?

What stereoisomers are obtained when (S)-3-methyl-1-pentene reacts with Cl2?

a. Is the reaction of 2-butene with HBr regioselective?

b. Is it stereoselective?

c. Is it stereospecific?

d. Is the reaction of 1-butene with HBr regioselective?

e. Is it stereoselective?

f. Is it stereospecific?

Draw the mechanism for the reaction of cyclohexene with HCl

Each of the following reactions has two nucleophiles that could add to the intermediate formed by the reaction of the alkene with an electrophile. What is the major product of each reaction
See all solutions

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