In the given esterification reaction,the labelled $^{18}O$ will be found in:

  • A
    $H_2O$
  • B
    Methyl benzoate
  • C
    Both $(a)$ and $(b)$
  • D
    Benzoic acid

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$A$ $\xleftarrow{CH_3OH, CH_3O^{-}}$ ($1$-methyl$-6-$oxabicyclo[$3.1$.$0$]hexane) $\xrightarrow{CH_3OH, H_2SO_4}$ $B$
$A$ $\&$ $B$ are :

Assertion: $tert$-Butyl methyl ether is not prepared by the reaction of $tert$-butyl bromide with sodium methoxide.
Reason: Sodium methoxide is a strong nucleophile.

Arrange the following sets of compounds in order of their increasing boiling points:
$(a)$ Pentan$-1-$ol,butan$-1-$ol,butan$-2-$ol,ethanol,propan$-1-$ol,methanol.
$(b)$ Pentan$-1-$ol,$n-$butane,pentanal,ethoxyethane.

Cyclohexanol and phenol can be distinguished by

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Match the structures in Column-$I$ with their common names in Column-$II$ and $\text{IUPAC}$ names in Column-$III$.
Column-$I$Column-$II$ (Common Name)Column-$III$ ($\text{IUPAC}$ Name)
$(A)$ Phenol$(1)$ Resorcinol$(i)$ Benzene$-1,2-$diol
$(B)$ Benzene$-1,3-$diol$(2)$ Catechol(ii) Phenol
$(C)$ Benzene$-1,2-$diol$(3)$ Phenol(iii) Benzene$-1,4-$diol
$(D)$ Benzene$-1,4-$diol$(4)$ Hydroquinone(iv) Benzene$-1,3-$diol

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