In an attempt to prepare n−propylbenzene, a chemist alkylated benzene with 1−chloropropane and aluminum chloride. However, two isomeric hydrocarbons were obtained in a ratio of 2:1, the desired n−propylbenzene being the minor component. What do you think was the major product? How did it arise?

Aluminum Chloride grasped the 1-chloropropane forming an intermediate product composed of Aluminum tetrachloride and n-propylcation. It is well understood that primary carbocations are unstable and therefore undergo hydrogen shifting to attain stability. n-Propylcarbocation undergone hydrogen shifting, forming isopropylcarbocation which reacted with benzene forming 2-Phenylpropane as the major product and HCl as a byproduct.

AlCl3 + CH3CH2CH2Cl --> AlCl4- + CH3CH2CH2+

CH3CH2CH2+ ---> CH3CH(+)CH3

C6H6 + CH3CH(+)CH3 ---> C6H5CH(CH3)2 + H+

AlCl4- + H+ ---> HCl + AlCl3

braza909 braza909 · Answer 2 · 2020-04-29T06:00:24+02:00

braza909 braza909

29-04-2020

Answer:

From the given problem statement,he was attempting to prepare n−propylbenzene by alkylation benzene with 1−chloropropane and aluminum chloride,but 1-propyle benze was a major product in result.

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