(a)
Interpretation: The products formed due to elimination and most likely mechanism for below reaction should be written.
Concept introduction: Carbocations generated from
If the leaving group present eliminates along with a proton in absence of any strong nucleophile the double bond formation might occur. Such reactions are known as two-step unimolecuar elimination, abbreviated as
(b)
Interpretation: The products formed due to elimination and most likely mechanism for below reaction should be written.
Concept introduction: Carbocations generated from alkyl halides have two fates; they can be either trapped by nucleophiles to give substitution product or may deprotonate to yield a small amount of alkene.
If the leaving group present eliminates along with a proton in absence of any strong nucleophile the double bond formation might occur. Such reactions are known as two-step unimolecuar elimination, abbreviated as
(c)
Interpretation: The products formed due to elimination and most likely mechanism for below reactionshould be written.
Concept introduction: Carbocations generated from alkyl halides have two fates; they can be either trapped by nucleophiles to give substitution product or may deprotonate to yield a small amount of alkene.
If the leaving group present eliminates along with a proton in absence of any strong nucleophile the double bond formation might occur. Such reactions are known as two-step unimolecuar elimination, abbreviated as
(d)
Interpretation: The products formed due to elimination and most likely mechanism should be written.
Concept introduction: Carbocations generated from alkyl halides have two fates; they can be either trapped by nucleophiles to give substitution product or may deprotonate to yield a small amount of alkene.
If the leaving group present eliminates along with a proton in absence of any strong nucleophile the double bond formation might occur. Such reactions are known as two-step unimolecuar elimination, abbreviated as
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Organic Chemistry: Structure and Function
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