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