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primary carbon + strong base and weak nucleophile
only E2
secondary carbon + strong base and weak nucleophile
only E2
tertiary carbon + strong base and weak nucleophile
only E2
primary carbon + strong base and strong nucleophile
SN2 and E2 but SN2 is favored
secondary carbon + strong base and strong nucleophile
SN2 and E2 but E2 is favored
tertiary carbon + strong base and strong nucleophile
E2 only
primary carbon + weak base and strong nucleophile
SN2 only
secondary carbon + weak base and strong nucleophile
SN2 only
tertiary carbon + weak base and strong nucleophile
SN1 only
primary carbon + weak base and weak nucleophile
no reaction
secondary carbon + weak base and weak nucleophile
no reaction
tertiary carbon + weak base and weak nucleophile
SN1 and E1 (50%)
Why does a primary and secondary carbon reacted with a weak nucleophile and weak base have no reaction?
The carbocation that is formed is too unstable