Kinetics E2 Nucleophile β- Elimination Antiperiplanar E1 Activation Energy Brønsted Base Aprotic Strong Base Second Order Methyl Intermediate Reactivity Minor Product Zero Order Electrophile Carbocation Zaitsev's Rule Mechanism 3° Nucleophilic Substitution Leaving Group Rate Law Weak Base Rate Constant SN2 Racemization Stereochemistry Backside Attack Polarizability Alkyl Halide First Order Hoffman's Rule Major Product Protic SN1 Bimolecular Base Regioselectivity Solvolysis Rate Determining Step 2° Gibbs Free Energy Change Steric Hindrance Reaction Order Unimolecular 1° Kinetics E2 Nucleophile β- Elimination Antiperiplanar E1 Activation Energy Brønsted Base Aprotic Strong Base Second Order Methyl Intermediate Reactivity Minor Product Zero Order Electrophile Carbocation Zaitsev's Rule Mechanism 3° Nucleophilic Substitution Leaving Group Rate Law Weak Base Rate Constant SN2 Racemization Stereochemistry Backside Attack Polarizability Alkyl Halide First Order Hoffman's Rule Major Product Protic SN1 Bimolecular Base Regioselectivity Solvolysis Rate Determining Step 2° Gibbs Free Energy Change Steric Hindrance Reaction Order Unimolecular 1°
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Kinetics
E2
Nucleophile
β-Elimination
Antiperiplanar
E1
Activation Energy
Brønsted Base
Aprotic
Strong Base
Second Order
Methyl
Intermediate
Reactivity
Minor Product
Zero Order
Electrophile
Carbocation
Zaitsev's Rule
Mechanism
3°
Nucleophilic Substitution
Leaving Group
Rate Law
Weak Base
Rate Constant
SN2
Racemization
Stereochemistry
Backside Attack
Polarizability
Alkyl Halide
First Order
Hoffman's Rule
Major Product
Protic
SN1
Bimolecular
Base
Regioselectivity
Solvolysis
Rate Determining Step
2°
Gibbs Free Energy Change
Steric Hindrance
Reaction Order
Unimolecular
1°