ng from 3-hexene? Br Br a. CH,CH,CHCHCH,CH; b. CH,CH,CH,CH,CH,CH, Cl c. CH,CH,CH,CHCH,CH, с. ОН d. CH;CH,CH,CHCH,CH,

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Chapter12: Unsaturated Hydrocarbons
Section: Chapter Questions
Problem 12.28E
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What reagents would you use to prepare each of the follow-
ing from 3-hexene?
Br Br
a. CH,CH,CHCHCH,CH;
b. CH,CH,CH,CH,CH,CH,
CI
c. CH,CH,CH,CHCH,CH,
OH
d. CH;CH,CH,CHCH,CH,
Transcribed Image Text:What reagents would you use to prepare each of the follow- ing from 3-hexene? Br Br a. CH,CH,CHCHCH,CH; b. CH,CH,CH,CH,CH,CH, CI c. CH,CH,CH,CHCH,CH, OH d. CH;CH,CH,CHCH,CH,
Expert Solution
Step 1

Reaction a. 

Reaction of alkene with Br2 reduces the double bond and forms a dibromo product 

Reaction b. 

Reaction of alkene with reducing agent Lindlar's catalyst (H2/Pd), reduces the double from same phase 

Reaction c. 

Hydrohalogenation of alkene 

Reaction of alkene with HCl forms a monochloro product via carbocation intermediate.

Reaction d.

Acid catalysed hydration of alkene. 

Reaction of alkene with H2SO4 (catalyst)followed by water forms alcohol.

 

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