Abstract
The infra-red spectra of o-nitroanilines
do not indicate any intramolecular hydrogen bonding unless there are nitro
groups in both positions 2 and 6 to the amino group. An examination of the
literature shows that there is no unambiguous evidence from other sources of
such bonding in simple o-nitroanilines. An explanation is given of the
variation of the stretching frequencies of the nitro group in sterically
hindered compounds and in those with electron-donating ortho- and
para-substituents.
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