Chemistry - Aromatic Hydrocarbon Question with Solution | TestHub

ChemistryAromatic HydrocarbonAROMATIC NUCLEPHIC SUBSTITUTION BY SNAE and SNEAEasy2 minPYQ_2024
ChemistryEasysingle choice

Which of the following compound will most easily be attacked by an electrophile?

Question diagram: Which of the following compound will most easily be attacked

Options:

Answer:
D
Solution:

Ortho, para directing groups are electron-donating groups; meta directing groups are electron-withdrawing groups. The halide ions, which are electron-withdrawing but ortho, para directing, are the exception.

Here -OH group is strong electron donating group. Hence electrophile can easily give electron.

-OH group in phenol can release electrons to the ring better than -CH3 group in toluene. Cl atom has electron withdrawing effect which inhibits electrophile attack readily.


Stream:JEESubject:ChemistryTopic:Aromatic HydrocarbonSubtopic:AROMATIC NUCLEPHIC SUBSTITUTION BY SNAE and SNEA
2mℹ️ Source: PYQ_2024

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