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SN1
two-step reaction where the leaving group leaves first to form a carbocation, then the nucleophile attacks the carbocation
SN2
one-step reaction where the nucleophile attacks from the backside as the leaving group departs, causing inversion of configuration
E1
two-step reaction where the leaving group leaves to form a carbocation, then a base removes a b-hydrogen to form a double bond
E2
one-step reaction where a strong leaving base removes a b-hydrogen at the same time the leaving group departs, forming a double bond in a single concerted step