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Question

Markovnikov’s rule:

Alkenes undergo electrophilic addition reactions. They are triggered by the acid acting as an electrophile toward the π-electrons of the double bond.

Markovnikov’s rule states that when an unsymmetrically substituted alkene reacts with a hydrogen halide, the hydrogen atom adds to the carbon that has a greater number of hydrogens, e.g.,

What is the energy profile of the given reaction?

A
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B
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C
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D
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Solution

The correct option is C
Markovnikov’s addition on alkene using HX is a 2 step process.
1st step involves the generation of carbocation and is a slow step whereas 2nd step involves attack of Nu(X) to form product and is a fast process.


The step with the largest activation energy will be the rate-determining step. In the figure, the second step has larger activation energy and is, therefore, the rate-determining step.

Energy profile of the given reaction has 2 peaks indicating 2 steps and 1st peak will be higher than 2nd indicating 1st step as slow.


So, the correct answer is (B).


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