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Question

Chemistry Question on Haloalkanes and Haloarenes

The ease of dehydrohalogenation of alkyl halide with alcoholic KOHKOH is

A

3o<2o<1o3^{o} < 2^{o} < 1^{o}

B

3o>2o>1o3^{o} > 2^{o} >1^{o}

C

3o<2o>1o3^{o} < 2^{o} > 1^{o}

D

3o>2o<1o3^{o} > 2^{o} < 1^{o}

Answer

3o>2o>1o3^{o} > 2^{o} >1^{o}

Explanation

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 (3)>\left(3^{\circ}\right)> secondary (2)>\left(2^{\circ}\right)> primary (1)\left(1^{\circ}\right)