In the given reaction sequence,Y is:Cyclohexa | vedclass

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(A) $1$. Cyclohexanol undergoes acid-catalyzed dehydration $(H^{\oplus}/\Delta)$ to form cyclohexene $(X)$.$2$. Cyclohexene then undergoes reductive o

Vedclass · Accepted Answer

$OHC-(CH_2)_4-CHO$

Vedclass · Answer

(A) $1$. Cyclohexanol undergoes acid-catalyzed dehydration $(H^{\oplus}/\Delta)$ to form cyclohexene $(X)$.$2$. Cyclohexene then undergoes reductive ozonolysis $((1) O_3, (2) H_2O/Zn)$ to break the double bond and form a dicarbonyl compound.$3$. The reaction is: Cyclohexene $\xrightarrow{O_3/Zn, H_2O}$ Hexanedial $(OHC-(CH_2)_4-CHO)$.$4$. Therefore,$Y$ is $OHC-(CH_2)_4-CHO$.

In the given reaction sequence,$Y$ is:
Cyclohexanol $\xrightarrow{H^{\oplus}/\Delta} X$ $\xrightarrow[(2) H_2O/Zn]{(1) O_3} Y$

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In the given reaction sequence,$Y$ is:Cyclohexanol $\xrightarrow{H^{\oplus}/\Delta} X$ $\xrightarrow[(2) H_2O/Zn]{(1) O_3} Y$