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