Ortho-nitrophenol is less soluble in water than $p-$ and $m-$nitrophenol because...

  • A
    $o-$nitrophenol has a lower melting point than $m-$ and $p-$isomers.
  • B
    $o-$nitrophenol is more steam volatile than $m-$ and $p-$isomers.
  • C
    $o-$nitrophenol shows intermolecular $H-$bonding.
  • D
    $o-$nitrophenol shows intramolecular $H-$bonding.

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Similar Questions

Viscosity of a liquid arises due to strong intermolecular forces existing between the molecules. Stronger the intermolecular forces,greater is the viscosity. Name the intermolecular forces existing in the following liquids and arrange them in the increasing order of their viscosities. Also give reason for the assigned order in one line.
Water,hexane $(CH_3CH_2CH_2CH_2CH_2CH_3)$,glycerine $(CH_2OHCH(OH)CH_2OH)$

What is the reason for the exceptionally high boiling point of water?

The incorrect order of boiling point is

Which concept best explains that $o-$nitrophenol is more volatile than $p-$nitrophenol?

Which of the following compounds in liquid state does not have hydrogen bonding?

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