Chemical Bonding
Intramolecular hydrogen bond is not present in:
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 :
Given molecular formula is $$C_9H_{18}O_3$$
Also, $$A$$ has higher boiling point than $$B$$.
So, for the given molecular formula we can write $$2$$ functional groups namely alcohol and ether.
And if we compared alcohol and ether in terms of their boiling point, ether has a very low boiling point than alcohols.
It is because in ethers there is no $$O-H$$ bond so it can form hydrogen bonding that is why it does not form hydrogen bonding.
But in case of alcohol, we have $$O-H$$ bond so it can form hydrogen bonding, that is why more amount of energy required to break the bonds so, more boiling point.
So, $$A$$ is alcohol and $$B$$ is ether.
Hence, option B is correct.
Intramolecular hydrogen bond is not present in:
The correct order of volalitity is:
Draw the structure of enol form of $$\displaystyle CH_3COCH_2COCH_3$$ with intramolecular hydrogen bonding.
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 :