Question Error Report

Thank you for reporting, we will resolve it shortly

Back to Question

Q. The ease of dehydrohalogenation of alkyl halide with alcoholic $KOH$ is

WBJEEWBJEE 2011Haloalkanes and Haloarenes

Solution:

According to Saytzeff rule, any alkyl halide that gives a more highly substituted (more stable) alkene undergoes dehydrohalogenation faster than the one which gives a less highly substituted (less stable) alkene. Thus, the ease of dehydrohalogenation of different alkyl halides having the same halogen decreases in the order tertiary $\left(3^{\circ}\right)>$ secondary $\left(2^{\circ}\right)>$ primary $\left(1^{\circ}\right)$