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I have an proton NMR for a compound that I believe to be Salicylic Acid. It...

I have an proton NMR for a compound that I believe to be Salicylic Acid. It has major peaks at 11.0 ppm as well as around 10.5 ppm. Both peaks are broad singlets indicating that they should be -OH peaks. However, the typical Phenol has a peak around 5-6 ppm. Could it be possible that the aromatic ring and carbonyl group from the carboxylic acid influenced the phenol group enough to shift it that far downfield?

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