(11) At position numbers 1, 2 and 5, the free radical will be stabilized by reso
ID: 700670 • Letter: #
Question
(11)
At position numbers 1, 2 and 5, the free radical will be stabilized by resonance on the adjacent benzene rings.
At position 3, the free radical will be stabilized because it is a tertiary free radical.
So the only position left is number 4, it is not stabilized by any resonance and also it is a primary free radical.
So the position which will be least susceptible to the substitution is number 4.
(12)
The molecules of o-nitrophenol show intra-molecular hydrogen bonding whereas the molecules of p-nitrophenol show inter-molecular hydrogen bonding. Hence o-nitrophenol is more steam volatile because of the presence of hydrogen bonding.
(14)
The typical reaction of a carbonyl group is an addition reaction proceeding through a nucleophilic attack. The reaction shown in option (A) is not a typical reaction for carbonyl group. The reaction in (B) is a typical reaction because it proceeds with a nucleophilic attack followed by the Beckmann Rearrangement reaction.
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