Chemical Bonding
Intramolecular hydrogen bond is not present in:
The correct order of volalitity is:
Stronger intermolecular forces would make the substance less volatile.
We see intermolecular H-bonding in para-nitro phenol ,so para-nitro phenol is less volatile, where as in o-nitro phenol, intra H-bonding takes places, thus, it is highly volatile.
Intramolecular hydrogen bond is not present in:
Draw the structure of enol form of $$\displaystyle CH_3COCH_2COCH_3$$ with intramolecular hydrogen bonding.
Among the compounds $$A$$ and $$B$$ with molecular formula $${C}_{9}{H}_{18}{O}_{3}$$, $$A$$ is having higher boiling point the $$B$$. The possible structures of $$A$$ and $$B$$ are :
The intramolecular hydrogen bonding in compound leads to:
Out of o-nitrophenol and p-nitrophenol which has higher boiling point and why ?
The boiling and melting points of water are abnormally higher than those of other hybrides of group 16 of the periodic table. Give reasons.
Which concept best explains that o-nitrophenol is more volatile than p-nitrophenol?
Which of the following compound can form hydrogen bonds?
Intramolecular hydrogen bond is present in:
Out of the two compounds shown above, the vapour pressure of B at a particular temperature is expected to be :