Ortho nitrophenol exhibits intramolecular hydrogen bonding. In the ortho isomer, the hydroxyl group (-OH) and the nitro group (-NO\(_2\)) are close enough in proximity for the hydrogen atom of the hydroxyl group to form a bond with the oxygen of the nitro group. This results in a stable structure with intramolecular hydrogen bonding.
On the other hand, para nitrophenol does not have this kind of interaction because the -OH and -NO\(_2\) groups are positioned far apart (in the para position), preventing the formation of intramolecular hydrogen bonds.
Thus, Ortho nitrophenol has intramolecular hydrogen bonding.