Foundation9 past questions

Reactive Intermediates: Carbocations, Carbanions, and Free Radicals

Learn about the structure, stability, and formation of carbocations, carbanions, and free radicals in organic reactions.

Why this shows up in the exam

You need to predict which intermediates are most stable and how they influence reaction pathways.

How NEET tests this

Direct recall · 5 QsApplication · 2 QsStatement analysis

Practise it

These are real questions from past NEET papers that test this exact idea.

Question 1 of 9NEET 1991

Which of the following is the most stable carbocation (carbonium ion)?

Push further

More challenging

3 harder questions built from the past papers above — a step up in difficulty, with distractors designed so you can't get there by elimination. Written and checked by our reviewers, not from a real paper.

Question 1 of 3

Consider the following statements regarding hyperconjugation in free radicals: (I) It involves the delocalization of sigma electrons of C-H bonds. (II) The stability of a radical increases with an increase in the number of alpha-hydrogens. (III) Benzyl radical (C₆H₅-CH₂•) is primarily stabilized by hyperconjugation. Which of the above statements are correct?