Challenging1 past question

Electronic Effects in Organic Molecules

Study the inductive, electromeric, resonance, and hyperconjugation effects and their influence on stability and reactivity of organic intermediates.

Why this shows up in the exam

These effects explain trends in stability and reactivity, which are commonly tested in mechanism and stability questions.

How NEET tests this

Statement analysis

Practise it

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

Question 1 of 1NEET 2023

Given below are two statements: Statement I : In an organic compound, when inductive and electromeric effects operate in opposite directions, the inductive effect predominates. Statement II : Hyperconjugation is observed in o-xylene. In the light of the above statements, choose the correct answer from the options given below:

Push further

More challenging

4 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 4

Which of the following statements correctly describes the interplay of electronic effects in stabilizing a carbocation? Statement I: Both inductive effect and hyperconjugation contribute to the stability of a carbocation, with hyperconjugation generally being the more dominant factor for alkyl carbocations. Statement II: A primary carbocation like CH3CH2+ is stabilized primarily by the +I effect of the methyl group, as it lacks sufficient alpha-hydrogens for significant hyperconjugation.