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The mechanism involved in the following conversion is 
  • a)
    E2  – elimination  
  • b)
    E1 – elimination    
  • c)
    Syn – elimination  
  • d)
    E1cb – elimination 
Correct answer is option 'D'. Can you explain this answer?
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Both the Cβ–H and Cα–X bonds are breaking in the transition state of E2 reactions. The rate of E2 reaction is of second order. The rate shows primary isotopic (deuterium) effect, i.e. if Cβ–H is replaced by Cβ–D, the rate of reaction decreases sharply. The rate is also corelated with nucleofugality i.e. the ability of leaving group to leave. With a better nucleofuge, the rate of reaction increases. This is called the element effect.The element effect is also observed in E1cB reactions in which the second step is rate determining and elimination of first order w.r.t. conjugate base is observed. For E1cB reaction KH/KD ~ 1, therefore proton abstraction is not involved in the rate determing step. In D2O the incorporation of Deuterium at Cβ–H in the substrate is found many times faster than rate of elimination, in E1cB reaction.In E1 reaction only nucleofuge departs in slow step and a carbocation intermediate is formed.Q.Consider the following statement, “In 80% aqueous ethanol, t-Butyl iodide solvolyses 100 times as rapidly as t-Butylchloride, but the ratio of elimination to substitution products is the same for chloride and iodide.” This statement indicates that

Both the Cβ–H and Cα–X bonds are breaking in the transition state of E2 reactions. The rate of E2 reaction is of second order. The rate shows primary isotopic (deuterium) effect, i.e. if Cβ–H is replaced by Cβ–D, the rate of reaction decreases sharply. The rate is also corelated with nucleofugality i.e. the ability of leaving group to leave. With a better nucleofuge, the rate of reaction increases. This is called the element effect.The element effect is also observed in E1cB reactions in which the second step is rate determining and elimination of first order w.r.t. conjugate base is observed. For E1cB reaction KH/KD ~ 1, therefore proton abstraction is not involved in the rate determing step. In D2O the incorporation of Deuterium at Cβ–H in the substrate is found many times faster than rate of elimination, in E1cB reaction.In E1 reaction only nucleofuge departs in slow step and a carbocation intermediate is formed.Q.Observe the given reaction. In this reactionWhat is not true about this reaction

Both the Cβ–H and Cα–X bonds are breaking in the transition state of E2 reactions. The rate of E2 reaction is of second order. The rate shows primary isotopic (deuterium) effect, i.e. if Cβ–H is replaced by Cβ–D, the rate of reaction decreases sharply. The rate is also corelated with nucleofugality i.e. the ability of leaving group to leave. With a better nucleofuge, the rate of reaction increases. This is called the element effect.The element effect is also observed in E1cB reactions in which the second step is rate determining and elimination of first order w.r.t. conjugate base is observed. For E1cB reaction KH/KD ~ 1, therefore proton abstraction is not involved in the rate determing step. In D2O the incorporation of Deuterium at Cβ–H in the substrate is found many times faster than rate of elimination, in E1cB reaction.In E1 reaction only nucleofuge departs in slow step and a carbocation intermediate is formed.Q.For the given compounds I and II the rate of elimination byWhat is true about this reaction

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The mechanism involved in the following conversion isa)E2 elimination b)E1 elimination c)Syn elimination d)E1cb eliminationCorrect answer is option 'D'. Can you explain this answer?
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The mechanism involved in the following conversion isa)E2 elimination b)E1 elimination c)Syn elimination d)E1cb eliminationCorrect answer is option 'D'. Can you explain this answer? for JEE 2024 is part of JEE preparation. The Question and answers have been prepared according to the JEE exam syllabus. Information about The mechanism involved in the following conversion isa)E2 elimination b)E1 elimination c)Syn elimination d)E1cb eliminationCorrect answer is option 'D'. Can you explain this answer? covers all topics & solutions for JEE 2024 Exam. Find important definitions, questions, meanings, examples, exercises and tests below for The mechanism involved in the following conversion isa)E2 elimination b)E1 elimination c)Syn elimination d)E1cb eliminationCorrect answer is option 'D'. Can you explain this answer?.
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Here you can find the meaning of The mechanism involved in the following conversion isa)E2 elimination b)E1 elimination c)Syn elimination d)E1cb eliminationCorrect answer is option 'D'. Can you explain this answer? defined & explained in the simplest way possible. Besides giving the explanation of The mechanism involved in the following conversion isa)E2 elimination b)E1 elimination c)Syn elimination d)E1cb eliminationCorrect answer is option 'D'. Can you explain this answer?, a detailed solution for The mechanism involved in the following conversion isa)E2 elimination b)E1 elimination c)Syn elimination d)E1cb eliminationCorrect answer is option 'D'. Can you explain this answer? has been provided alongside types of The mechanism involved in the following conversion isa)E2 elimination b)E1 elimination c)Syn elimination d)E1cb eliminationCorrect answer is option 'D'. Can you explain this answer? theory, EduRev gives you an ample number of questions to practice The mechanism involved in the following conversion isa)E2 elimination b)E1 elimination c)Syn elimination d)E1cb eliminationCorrect answer is option 'D'. Can you explain this answer? tests, examples and also practice JEE tests.
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