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