Answer
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Hint: Addition reaction is a type of reaction in which one compound is added to another to combine and form the product. Along with addition, rearrangement of carbocation takes place, in which the proton that is H atom is transferred to form a short-lived intermediate which further can lead to structural rearrangement of the molecule to obtain a larger yield.
Complete step-by-step answer:When an addition reaction is performed on alkene by adding strong acids like HBr, HI, HCl, etc. the C=C bond is broken to form new covalent bonds with the hydrogen and conjugate base of the acid. The general reaction will be,
In this example, that is 3-methyl-1-butene, the C involved in double bonds are structurally unsymmetrical, hence a reaction with a strong acid like HCl will give two products in different quantities. This is because of the rearrangement of the carbocation.
Mechanism of the reaction:
Hence, the correct option is option A - Both Assertion and Reason are correct and Reason is the correct explanation for Assertion.
Note:In this reaction that is the reaction of unsymmetrical alkene when reacts with HCl the double bond that is protonated will form a major product fast due to stable carbocation rearrangement compared to the other product.
Complete step-by-step answer:When an addition reaction is performed on alkene by adding strong acids like HBr, HI, HCl, etc. the C=C bond is broken to form new covalent bonds with the hydrogen and conjugate base of the acid. The general reaction will be,
In this example, that is 3-methyl-1-butene, the C involved in double bonds are structurally unsymmetrical, hence a reaction with a strong acid like HCl will give two products in different quantities. This is because of the rearrangement of the carbocation.
Mechanism of the reaction:
Hence, the correct option is option A - Both Assertion and Reason are correct and Reason is the correct explanation for Assertion.
Note:In this reaction that is the reaction of unsymmetrical alkene when reacts with HCl the double bond that is protonated will form a major product fast due to stable carbocation rearrangement compared to the other product.
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