The product $(X)$ is:

  • A
    $4-$ethylcyclohex$-1-$ene with a methoxymethyl ether group
  • B
    cis$-4-$ethylcyclohex$-1-$ene with a methoxy group
  • C
    trans$-4-$methylcyclohex$-1-$ene with an ethoxymethyl ether group
  • D
    cis$-4-$methylcyclohex$-1-$ene with an ethoxy group

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Similar Questions

Predict the major product of the reaction:

Consider the following sequence of reactions:
Nitrobenzene $\xrightarrow[(ii) NaNO_2, HCl, 0^{\circ}C]{(i) Sn + HCl} \text{Benzenediazonium chloride}$ $\xrightarrow{(iii) Cu_2Cl_2} \text{Chlorobenzene}$ $\xrightarrow{(iv) Na, \text{Ether}} A$
Molar mass of the product formed $(A)$ is $.............. \ g \ mol^{-1}$.

In the following reaction sequence, $X$ and $Z$, respectively, are:
$CH_{3}CH_{2}CH_{2}-OH + PCl_{5} \rightarrow CH_{3}CH_{2}CH_{2}Cl + X + HCl$
$CH_{3}CH_{2}CH_{2}Cl \xrightarrow{alc. KOH, \Delta} Y$
$Y \xrightarrow{HBr, (C_{6}H_{5}CO)_{2}O_{2}} Z$

The product$(s)$ formed during the following reaction is/are:
$Ph-CH_2-C^*H_2-OTs \xrightarrow{AcONa, AcOH} \text{Product(s)} \ [C^* = \text{isotopic carbon}]$

Given below are two statements:
Statement $I$: $3$-phenylpropene reacts with $HBr$ and gives secondary alkyl bromide having a chiral carbon atom as the major product.
Statement $II$: Aryl chlorides and aryl cyanides can be prepared by Sandmeyer reaction as well as Gattermann reaction.

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