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