Capítulo 03
Chlorination of Methane
Capítulo 04
Cyclohexane Ring Flip
Cyclohexane Potential Energy Diagram
Chlorination of Methane
Cis-Dimethylcyclohexane
Trans-dimethylcyclohexane
Capítulo 06
Does concerted attack occur from the front?
Concerted attack on a chiral R reactant from the front gives an R product
Concerted attack on a chiral R reactant from the back gives an S product
Reaction mechanism shown in symbolic detail
Change in potential energy during reaction mechanism
Ball & stick and space-filling representations of reaction mechanism
Role of methanol solvent in reducing nucleophilicity
Role of DMF solvent in increasing nucleophilicity
Capítulo 07
Reaction mechanisms shown in symbolic detail
Change in potential energy during reaction mechanism
Ball & stick representation of back- and frontside nucleophilic attack
Reaction mechanism shows why a chiral reactant leads to a racemic product
Reaction mechanism shown in symbolic detail
Ball & stick and space-filling representations of reaction mechanism
Capítulo 08
Reduction of cyclobutanone with lithium aluminum hydride
Formation of Grignard reagent from 1-bromobutane and reaction with acetaldehyde to give 2-hexanol
Reduction of pentanal with sodium borohydride
Capítulo 09
Mechanism of alcohol dehydration
Mechanism of carbocation rearrangement
Capítulo 12
Reaction mechanism shown in symbolic detail
Ball & stick and space-filling representations of reaction mechanism
Mechanism of hydroboration-odation
Oacyclopropanation
Mechanism of ozonolysis
Radical hydrobromination of propene
Brominationofcis-2-butene
Brominationoftrans-2-butene
Cyclobutene
Stereospecific bromination of 2-butenes
Capítulo 14
Addition of HBr to 1,3-butadiene
Cis-dimethylcyclobutene
Trans,cis,trans-2,4,6-Octatriene
Mechanism of the Diels-Alder cycloaddition (endo rule)
Radical allylic halogenation
Diels-Aldercis,cis-hexadieneexoendo
Diels-Aldercis,trans-hexadieneexoendo
Diels-Aldertrans,trans-hexadieneexoendo
Diels-AldercyclopentadieneDMAD
Diels-AlderCyclpentadieneMAeoendo
Heatrieneclosure
Capítulo 15
Electrophilic aromatic sulfonation of benzene 1
Electrophilic aromatic sulfonation of benzene 2
Capítulo 16
Electrophilic aromatic substitution of benzenamine (ortho vs meta vs para)
Electrophilic aromatic substitution of benzoic acid (ortho vs meta vs para)
Capítulo 17
Mechanism of the Wittig reaction
Mechanism of acetal formation
Capítulo 18
Mechanism of the aldol condensation-dehydration
Mechanism of Robinson annulation: i.e. Michael addition followed by intramolecular aldol condensation
Capítulo 19
Mechanism of esterification
Capítulo 20
Amide hydrolysis
Hofmann rearrangement
Capítulo 21
Mechanism of reductive amination
Mechanism of the Mannich reaction
Capítulo 22
Nucleophilic Aromatic Substitution
Reaction of Benzylic nucleophilic substitution
Nucleophilic Aromatic Substitution via Benzynes
Cope
Claisen
Capítulo 23
Mechanism of the Claisen condensation
Capítulo 24
Methyl Glycoside Formation
Cyclic hemiacetal formation by glucose
Capítulo 26
Chapter 26: Mechanism of the Strecker synthesis