
Assertion:The addition of HCl to 3-methyl-1-butene gives 2-chloro-2-methyl butane as the major product.
Reason:Rearrangement of carbocation to move stable carbocation leads to the formation of a major product.
A.Both Assertion and Reason are correct and Reason is the correct explanation for Assertion.
B.Both Assertion and Reason are correct but Reason is not the correct explanation for Assertion.
C.Assertion is correct but Reason is incorrect.
D.Both Assertion and Reason are incorrect.
Answer
526.2k+ views
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.
Recently Updated Pages
Master Class 11 Social Science: Engaging Questions & Answers for Success

Master Class 11 Physics: Engaging Questions & Answers for Success

Master Class 11 Maths: Engaging Questions & Answers for Success

Master Class 11 Economics: Engaging Questions & Answers for Success

Master Class 11 Computer Science: Engaging Questions & Answers for Success

Master Class 11 Chemistry: Engaging Questions & Answers for Success

Trending doubts
What is meant by exothermic and endothermic reactions class 11 chemistry CBSE

10 examples of friction in our daily life

Difference Between Prokaryotic Cells and Eukaryotic Cells

1 Quintal is equal to a 110 kg b 10 kg c 100kg d 1000 class 11 physics CBSE

One Metric ton is equal to kg A 10000 B 1000 C 100 class 11 physics CBSE

Draw a diagram of a plant cell and label at least eight class 11 biology CBSE

