AIIMS 2019 Chemistry Carbocation Rearrangement MCQ Question





Correct Answer
Detailed Explanation
Option B is correct because it represents the final product formed after a carbocation rearrangement, where a more stable tertiary carbocation is generated, leading to the formation of a more substituted alkene through elimination. The other options are incorrect as they either depict intermediates that do not reflect the final product after rearrangement or show products that lack the necessary stability or structural features expected from the reaction sequence. Understanding carbocation stability and the mechanism of elimination reactions is crucial in predicting the major product in organic synthesis.
Found an issue with this question?
Related Questions
More from Organic Chemistry
CH₃OC₂H₅ and (CH₃)₃C – OCH₃ are treated with concentrated acidic iodide. The fragments after reactions obtained are
Arrange the following alkyl halides in decreasing order of the rate of β-elimination reaction with alcoholic KOH.
What happens when a carboxylic acid is treated with lithium aluminium hydride?