Question:

The boiling point of $p$-nitrophenol is higher than that of $o$-nitrophenol because

Updated On: Jul 28, 2022
  • intramolecular hydrogen bonding exists in $p$-nitrophenol
  • $-NO_2$ group at $p$-position behaves in a different way from that at $o$-position
  • $p$-nitrophenol has a higher molecular weight than $o$-nitrophenol
  • there is intermolecular hydrogen bonding in $p$-nitrophenol
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The Correct Option is D

Solution and Explanation

$p$-Nitrophenol has intermolecular hydrogen bonding so it has more boiling point and less volatile than $o$-nitrophenol which has intramolecular hydrogen bonding.
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Concepts Used:

Phenols

Phenol is a different class of organic compounds that are usually found in wide usage in an extensive range of industries and also for domestic purposes. Phenol is formed when a hydrogen atom in a benzene molecule is replaced by the chemical -OH group.

Phenol is also called as Carbolic acid. It is an aromatic organic compound having the molecular formula C6H5OH. It is a volatile white crystalline solid. The molecule consists of a phenyl group (−C6H5) bonded to a hydroxy group (−OH). Phenol is mildly acidic, it requires careful handling because it can cause chemical burns.

Classification of Phenol

On the basis of the different number of hydroxyl groups attached, the phenols can be classified further into three types.

  • Monohydric phenols: These contain one -OH group.
  • Dihydric phenols: These contain two -OH groups. These may be ortho-, meta- or para- derivative.
  • Trihydric phenols: These contain three -OH groups.

Properties of Phenol

  1. Phenol is an organic compound that is appreciably soluble in water, with about 84.2 g dissolving in 1000 mL (0.895 M).
  2. It is a weak acid.  
  3. is highly reactive toward electrophilic aromatic substitution.