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