stability of carbocation carbanion and free radicals#!#Inductive effect

|| |nductive effect application-stability comparision OF carbocation carbon free radical and carboxine ||

(GOC) : stability OF carbanion and free radicals,hyperconjugation in alkenes stability,heat OF hydrogenation

The most Carbocations, carbanions, free radicals and radical cation are reactive carbon intermediates. Their hybrid orbitals respectively are

An organic reaction occurs by using reagents called electrophiles and nucleophiles via the formation of some reactive intermediates called carbocations, carbanions, free radicals, carbenes, nitrenes, radical cations, and radical anions. The most stable carbanion is :

An organic reaction occurs by using reagents called electrophiles and nucleophiles via the formation of some reactive intermediates called carbocations, carbanions, free radicals, carbenes, nitrenes, radical cations, and radical anions. The most stable free radical is :

An organic reaction occurs by using reagents called electrophiles and nucleophiles via the formation of some reactive intermediates called carbocations, carbanions, free radicals, carbenes, nitrenes, radical cations, and radical anions. The most stable carbocation is :