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