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An alkene "A" on reaction with O3 and Zn...

An alkene "A" on reaction with `O_3` and Zn gives propanone and ethanol in equimolar Addition of HCl to alkene "A" gives "B" as the product. The structure of product "B" is:

A

`H_(3)C-underset(Cl)underset(|)(CH)-underset(CH_(3))underset(|)overset(CH_(3))overset(|)(CH)`

B

`Cl-CH_(2)-CH_(2)-underset(CH_3)underset(|)overset(CH_(3))overset(|)(CH)`

C

D

`H_(3)C-CH_(2)-underset(Cl)underset(|)overset(CH_(3))overset(|)(C)-CH_(3)`

Text Solution

Verified by Experts

The correct Answer is:
D


`A=CH_(3)-underset(CH_(3))underset(|)(C)=CH-CH_(3)`
`B=CH_(3)-underset(CH_(3))underset(|)overset(Cl)overset(|)(C)-CH_(2)-CH_(3)`
Formation of B from A is markonikoff rule addition by E.A.R mechanism
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