Action of hydrogen chloride on $CH_3-C(CH_3)=CH_2$ and on $CH \equiv CH$ will predominantly give the compounds,respectively:

  • A
    $CH_3-CH(CH_3)-CH_2Cl$ and $CH_2Cl-CH_2Cl$
  • B
    $CH_3-CCl(CH_3)-CH_3$ and $CH_3-CHCl_2$
  • C
    $CH_3-CH(CH_3)-CH_2Cl$ and $CH_3-CHCl_2$
  • D
    $CH_3-CH(CH_3)-CH_3$ and $CH_2Cl-CH_2Cl$

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The major product $[R]$ in the following sequence of reactions is :-

Match the following reactions in List-$I$ with their products in List-$II$:
List-$I$List-$II$
$A$. The reaction of $1,6$-dibromohexane with $Zn$.$i$. $H_3C-C \equiv CH$
$B$. Reaction of ethanol with concentrated $H_2SO_4$ at $443 \ K$.$ii$. $H_2C=CH_2$
$C$. Major product in the reaction of propene with $HBr$ in the presence of benzoyl peroxide.$iii$. $CH_3-CH_2-CH_2-Br$
$D$. The reaction of $1,1$-dibromopropane with $NaNH_2$ at $433 \ K$.$iv$. Cyclohexane

"$P$" is a hydrocarbon with the molecular formula $C_8H_{14}$. On ozonolysis,"$P$" forms "$Q$". "$Q$" on treatment with alkali under reflux conditions produces "$R$",which on treatment with $I_2/NaOH$ gives a yellow precipitate. Acidification of the solution gives "$S$". The structure of "$S$" is given below:
(Structure $S$: $1-$methyl$-2-$oxocyclopentanecarboxylic acid derivative or similar cyclic structure as per common reaction pathways).
The correct structure of "$P$" is:

Which of the following reagents will convert glycerol into acrolein?

Difficult
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The product$(s)$ from the above reaction will be

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