Put a circle around the statements that relate to an SN 2 mechanism and put a square around the ones that talk about SN1.
CH3X > 1˚ > 2˚ No rearrangements
Rearranged products Rate = k [alkyl halide] [Nuc]
Polar protic solvent Racemization
Inversion at chiral carbon Rate = k [alkyl halide]
3˚ > 2˚ Polar aprotic solvent
Strong nucleophile Weak nucleophile (may also be solvent)
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