What is the correct order of stability for the following alkenes?

  • A
    $1$-Butene > trans-$2$-Butene > cis-$2$-Butene
  • B
    trans-$2$-Butene > $1$-Butene > cis-$2$-Butene
  • C
    trans-$2$-Butene > cis-$2$-Butene > $1$-Butene
  • D
    cis-$2$-Butene > trans-$2$-Butene > $1$-Butene

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When neopentyl alcohol is heated with an acid,it slowly converts into an $85:15$ mixture of alkenes $A$ and $B$,respectively. What are these alkenes $?$ (Note: $A$ is the major product and $B$ is the minor product.)

What is the product obtained when an alkene is reacted with cold and dilute alkaline potassium permanganate $(KMnO_4)$?

Consider compounds $A$, $B$ and $C$ with following structural formulae: $A = CH_{3} - CH_{2} - CH_{2} - CH_{2} - CH_{2} - OH$, $B = CH_{2} = CH - CH_{2} - CH_{2} - CH_{3}$, $C = HO - CH_{2} - CH_{2} - CH(OH) - CH_{3}$. For the conversion of $B$ from $A$, reagent $(D)$ required is . . . . . . and structural formula of product $(E)$ obtained when $C$ undergoes same reaction using excess reagent $(D)$ is . . . . . . .

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Which of the following alkenes reacts fastest with $H_2$ under catalytic hydrogenation conditions?

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