An unknown alkene $(A)$ reacts with $3 \ mole$ of $H_2$ gas in the presence of a platinum catalyst to form $1$-isopropyl-$4$-methylcyclohexane. When the unknown alkene $(A)$ is ozonized and reduced,the following products are obtained:
$HCHO$,$OHC-CH_2-CO-CO-CH_3$,and $CH_3-CO-CH_2-CHO$
What is the structure of alkene $(A)$?

  • A
    Limonene ($1$-methyl$-4-$(prop$-1-$en$-2-$yl)cyclohex$-1-$ene)
  • B
    $1-$methyl$-4-$(prop$-1-$en$-2-$yl)cyclohex$-1,3-$diene
  • C
    $1-$isopropylidene$-4-$methylcyclohexa$-2,5-$diene
  • D
    $4-$methylene$-1-$(prop$-1-$en$-2-$yl)cyclohex$-1-$ene

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Similar Questions

The correct statement$(s)$ for the following addition reactions is(are):
$(i)$ $trans-but-2-ene \xrightarrow{Br_2/CHCl_3} M \text{ and } N$
(ii) $cis-but-2-ene \xrightarrow{Br_2/CHCl_3} O \text{ and } P$
[$A$] ($M$ and $O$) and ($N$ and $P$) are two pairs of diastereomers
[$B$] Bromination proceeds through trans-addition in both the reactions
[$C$] $O$ and $P$ are identical molecules
[$D$] ($M$ and $O$) and ($N$ and $P$) are two pairs of enantiomers

Electrophilic addition on a carbon-carbon double bond involves the intermediate formation of a more stable carbocation. This statement is called

$cis-3-hexene \xrightarrow{(a)} \text{meso } 3,4-hexanediol$
$trans-3-hexene \xrightarrow{(b)} \text{meso } 3,4-hexanediol$
Choose the pair of reagents $(a, b)$ for the above conversions.

The major product of the following reaction is $CH_3-CH(Br)-CH_2-CH_3 + \text{alc. } KOH \to $

In the given reaction,only one alkene undergoes preferential oxidation by electrophilic ozone. Identify the product $(P)$ of the given reaction.

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