Isomerism and StereochemistryhardMCQ SINGLE

Which of the following structural or energetic constraints severely prevents the formation of a stabIsomerism and Stereochemistry Chemistry Question

Question

Which of the following structural or energetic constraints severely prevents the formation of a stable enol tautomer in rigid bicyclic ketones like bicyclo[2.2.1]heptan-2-one?

Answer: B

💡 Solution & Explanation

According to Bredt's rule, placing a $sp^2$ hybridized double bond at the bridgehead of small bicyclic systems creates immense angle strain, forcing an impossible planar geometry. Thus, even if an acidic $\alpha$ -hydrogen is present at the bridgehead position, it cannot participate in keto-enol tautomerism.

💬
Still have doubts about this question?
Send it to our AI chemistry tutor on WhatsApp — gets answered in minutes
Ask on WhatsApp →

Practice 22,000+ questions like this

AI-adaptive practice, video lectures, and full JEE Advanced Chemistry content — all in one place.

JEE Advanced · JEE Mains · NEET · IChO · AP Chemistry