Reaction Intermediate|Word Meaning|Nucleophile|Electrophile|Bond Breakage|Carbocation - Formation|OMR

Word Formation|OMR

Reaction OF carbocation with Base and Nucleophile

Reaction Intermediate, Carbocation General Point || Stereochemistry Related To Carbocation

Reaction Intermediates|| Carbocation|| Stability OF Carbocation|| Rearrangement OF Carbocation (Hydride, Alkyl and Phenyl shift Reaction)

Electrophiles || Nucleophiles || Types OF Reactions

Types OF Reactions||electrophile|| Nucleophile and Free radical Reaction

Aldehydes and ketones undergo nucleophilic/electrophilic addition reactions.

Electrophilic Addition Reactions (Classical Carbocation)

Passage Organic compounds mainly consist of covalent bonds. The electron pair in these covalent bonds may undergo displacement either of their own or under the influence of other species. The cleavage of covalent bond between two atoms takes place in homolytic or heterolytic fashion. The homolytic fission results into free radicals while heterolytic fission results into carbocations and carbanions. These are also called reaction intermediates and are attacked by electrophiles and nucleophiles. The electrophiles seek electron rich sites while nucleophiles seek electron deficient sites. Answer the followings Questions : The most stable carbocation is :

Passage Organic compounds mainly consist of covalent bonds. The electron pair in these covalent bonds may undergo displacement either of their own or under the influence of other species. The cleavage of covalent bond between two atoms takes place in homolytic or heterolytic fashion. The homolytic fission results into free radicals while heterolytic fission results into carbocations and carbanions. These are also called reaction intermediates and are attacked by electrophiles and nucleophiles. The electrophiles seek electron rich sites while nucleophiles seek electron deficient sites. Answer the followings Questions : Which of the following is most stable carbocation ?