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(D) The conversion involves the following steps:$1$. Ozonolysis $(O_3/Zn)$ of $1,2$-dimethylcyclohexene yields $2,6$-heptanedione.$2$. Intramolecular

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$1 	o 2 	o 3 	o 4$

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(D) The conversion involves the following steps:$1$. Ozonolysis $(O_3/Zn)$ of $1,2$-dimethylcyclohexene yields $2,6$-heptanedione.$2$. Intramolecular aldol condensation $(EtONa/EtOH/\Delta)$ converts the diketone into a cyclic $\alpha,\beta$-unsaturated ketone.$3$. Haloform reaction $(NaOCl)$ converts the methyl ketone group into a carboxylic acid group.$4$. Acidification $(H^{+})$ yields the final product,$2$-methylcyclohex$-1-$ene$-1-$carboxylic acid.

To carry out the following conversion,arrange the reagents in the correct order:
$O_3/Zn$ $(1)$
$EtONa/EtOH/\Delta$ $(2)$
$NaOCl$ $(3)$
$H^{+}$ $(4)$

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To carry out the following conversion,arrange the reagents in the correct order:$O_3/Zn$ $(1)$$EtONa/EtOH/\Delta$ $(2)$$NaOCl$ $(3)$$H^{+}$ $(4)$