The compound which reacts with excess bromine to produce $2,4,6$-tribromophenol is

  • A
    $1,3$-cyclohexadiene
  • B
    $1,3$-cyclohexanedione
  • C
    salicylic acid
  • D
    cyclohexanone

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Ortho and para nitrophenols are more acidic than phenol. Draw the resonance structures of the corresponding phenoxide ions.

The main product of the following reaction will be:

The reaction sequence is as follows:
$Catechol \xrightarrow{(i) CHCl_3 + KOH}{(ii) CH_2I_2 + NaOH} [X]$
Here $[X]$ is:

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Arrange the following compounds in decreasing order of their acidity.

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Phenol can be distinguished from ethanol by the reagent

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