GOC and Organic Chemistry BasicsmediumMCQ SINGLE

The reaction of chloroform () with a strong base (such as or ) proceeds via an -elimination mechanisGOC and Organic Chemistry Basics Chemistry Question

Question

The reaction of chloroform ($CHCl_3$) with a strong base (such as $NaOH$ or $KOH$) proceeds via an $\alpha$ -elimination mechanism. What is the highly reactive intermediate generated in this process?

Answer: C

💡 Solution & Explanation

The base abstracts the acidic proton from chloroform to form $CCl_3^-$, which rapidly loses a chloride ion ($Cl^-$) in an $\alpha$ -elimination step to generate the neutral, electron-deficient electrophile, dichlorocarbene ($:CCl_2$).

💬
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 Mains Chemistry content — all in one place.

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