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SN2 reacts fastest with what alkyl halide
CH3>1>2
kinetics for SN2
r=k[E+][Nu-]
stereochemistry for SN2
inversion
Nucleophile for SN2
strong nucleophile
solvent for SN2
polar aprotic solvent
temperature for SN2
room temp
SN1 reacts fastest with what alkyl halide
3>2
kinetics for SN1
r=k[E+]
stereochemistry for SN1
racemization
nucleophile for SN1
weak
solvent for SN1
polar protic
temperature for SN1
room temp
E2 reacts fastest with what alkyl halide
3>2>1
kinetics for E2
r=k[RX][B]
stereochemistry for E2
antiperiplanar for acyclic molecules, transdiaxial for cyclic structures
base for E2
strong base
solvent for E2
polar aprotic
temperature for E2
>50C
E1 reacts fastest with what alkyl halide
3>2
kinetics for E1
r=k[RX]
stereochemistry for E1
none
base for E1
weak
solvent for E1
polar protic
temperature for E1
>50C