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Why is picric acid not more steam volatile than p-nitrophenol, if intramolecular bonding results in increased steam volatility?

I understand that relative to p-nitrophenol, o-nitrophenol would be more steam volatile (as p-nitrophenol can form intermolecular hydrogen bonds), but my question lies in the fact that its volatile ...
rania h's user avatar
6 votes
0 answers
1k views

Diazo Coupling reaction with para-substituted phenol?

Usually Diazo coupling occurs at para-position unless the para-position is occupied, in which case coupling occurs at ortho-position. While solving questions I found in both the cases as shown, the ...
Chloritone_360's user avatar
0 votes
3 answers
876 views

Is there an intramolecular hydrogen bond in guaiacol?

Is there a hydrogen bond between the $\ce{H}$ atom of $\ce{-OH}$ group and the $\ce{O}$ atom of the $\ce{-OCH3}$ group in ortho-methoxyphenol? I was told no. But I want to know why.
Govind Balaji S's user avatar
0 votes
2 answers
605 views

Organic problem: acidity of benzene substituents

Ortho nitro benzoic acid is more acidic than para benzoic acid since intermolecular H bonding comes into play in the latter compound. But why is that among para nitro phenol and ortho nitro phenol, ...
Harini's user avatar
  • 313
21 votes
5 answers
10k views

Strength of hydrogen bonding in phenol or methanol

I wanted to know whether hydrogen bonding is stronger in phenol or methanol. I saw on Wikipedia about the enthalpies of hydrogen bonding in various cases. but could not find the answer to this ...
Sugandha Gupta's user avatar