Consider the following compound:

Which of the following staements are correct?

Options

A. Loss of `Br(a)` atom in dehydrobrobromination reaction results in the formation of the most reactive double bond towards hydrogentaion reaction.
B. Removel of `Br(c)` atom results in the formaion of the most stable carbocation.
C. The above compound conatins five asymmetric `C` atoms.
D. The above compound does not show geometrical isomers.

Answer

`(a,b,c)`

Explanation

a. Loss of `Br(a)` would give less-subsituted alkene (more reactive, less stable).
b. Removel of `Br(c)` would give stable `2^(@)` allylic `C^(o+)`.
c.
Statemtents (a),(b) and (c) are correct.
Statements (d) is wrong, Since teh compound shows `G,I`.