Question

in which compound addition reaction will take place according to markovnikov's rule.​

Answer 1

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Explanation:

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Answer 2

Answer:

Concept:
While the halide group attaches to the carbon atom with the most alkyl substituents when a protic acid (HX) is introduced to an asymmetric alkene, the acidic hydrogen adheres to the carbon with the most hydrogen substituents.

Explanation:

“Hydrogen is added to the carbon with the most hydrogens and the halide is added to the carbon with the least hydrogens”

               

                    $\mathrm{CH}_{3}-\mathrm{CH}=\mathrm{CH}_{2}+\mathrm{HBr}$

compound addition reaction will take place according to markovnikov's rule in the above chemical equation.

Let's think about the addition reaction when an alkene and water combine to form alcohol. A carbocation is formed as this reaction progresses. In this reaction, the hydrogen atom joins to the other carbon in the double bond, which has more carbon-hydrogen bonds, whereas the hydroxyl group attaches to the carbon with more carbon-carbon bonds.

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