Chemistry - GOC Question with Solution | TestHub

ChemistryGOCAromaticityEasy2 minQB
ChemistryEasymultiple choice

Which member of each of the following pairs is more readily deprotonated ? Choose the correct pair(s).

(A) structure structure

(B) structure structure

(C) structure structure

Options:(select one or more)

Answer:
A, C
Solution:

(A) deprotonating cyclopentadiene gives the aromatic cyclopentadienyl anion (6π), while benzene would give an unstabilised aryl anion : correct. (B) cycloheptatriene gives an anti-aromatic 8π anion but still has an C-H that is far more acidic than any vinylic C-H of cyclooctatetraene, so the order shown is wrong. (C) cyclopropene gives the anti-aromatic cyclopropenyl anion (4π), so cyclopentadiene is more readily deprotonated : correct. Correct pairs : A and C.

Stream:JEESubject:ChemistryTopic:GOCSubtopic:Aromaticity
⏱ 2mℹ️ Source: QB

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