"$P$" is a hydrocarbon with the molecular formula $C_8H_{14}$. On ozonolysis,"$P$" forms "$Q$". "$Q$" on treatment with alkali under reflux conditions produces "$R$",which on treatment with $I_2/NaOH$ gives a yellow precipitate. Acidification of the solution gives "$S$". The structure of "$S$" is given below:
(Structure $S$: $1-$methyl$-2-$oxocyclopentanecarboxylic acid derivative or similar cyclic structure as per common reaction pathways).
The correct structure of "$P$" is:
(Structure $S$: $1-$methyl$-2-$oxocyclopentanecarboxylic acid derivative or similar cyclic structure as per common reaction pathways).
The correct structure of "$P$" is:
- A
- B
- C
- D
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| List-$I$ | List-$II$ |
|---|---|
| $A$. The reaction of $1,6$-dibromohexane with $Zn$. | $i$. $H_3C-C \equiv CH$ |
| $B$. Reaction of ethanol with concentrated $H_2SO_4$ at $443 \ K$. | $ii$. $H_2C=CH_2$ |
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