Chm 2120 Final Exam
ORGANIC CHEMISTRY II
Need to study the following:
- Reasonance Criteria:
- Base (proton acceptor/electron donor)
- Direction of Equilibrium
- SN2, E2, SN1/E1 Reactions
- Electrophilic Addition to alkenes
- Epoxides
- Nucleophile: donates electrons
- Electrophile: accepts electrons
- Memorize pKa's
- Nonmenclature (functional groups and benzene/common names)
- Aromatic Compounds (What makes a ring aromatic)
- Electrophilic Aromatic Substitution (EAS)
- Memorize the following mechanisms for these reactions:
- Memorize manipulation of aromatic substituents
- Side chain modifications
- Synthesis
- IR & NMR
Carbonyl Chemistry:
- Oxidation of alcohols
- Strongly Nucleophilic Conditions
- Acetals
- Wittig Reactions (E: trans, Z: cis)
- Baeyer-Villiger Oxidation
- Enols and Enolates
- Equilibrium is catalyzed by acid or base
- Esterification
- Fischer Esterification
- Ester hydrolysis (saponification)
- Acid Chlorides
- Andydrides
Looks like I have a lot ahead of me before friday
Need to study the following:
- Reasonance Criteria:
- All atoms have full octets
- Fewest charges
- (-) on electronegative atom, (+) on the electropositive atom
- Max sepsration of identical charges
- Min separation of opposite charges
- Base (proton acceptor/electron donor)
- Direction of Equilibrium
- SN2, E2, SN1/E1 Reactions
- Electrophilic Addition to alkenes
- Epoxides
- Nucleophile: donates electrons
- Electrophile: accepts electrons
- Memorize pKa's
- Nonmenclature (functional groups and benzene/common names)
- Aromatic Compounds (What makes a ring aromatic)
- Electrophilic Aromatic Substitution (EAS)
- Memorize the following mechanisms for these reactions:
- Nitration
- Sulfonation
- Halogenation
- Friedel-Crafts Alkylation
- Friedel-Crafts Acylation
- Activating Substituents
- Halides
- Memorize manipulation of aromatic substituents
- Side chain modifications
- Synthesis
- IR & NMR
Carbonyl Chemistry:
- Oxidation of alcohols
- Strongly Nucleophilic Conditions
- Acetals
- Wittig Reactions (E: trans, Z: cis)
- Baeyer-Villiger Oxidation
- Enols and Enolates
- Equilibrium is catalyzed by acid or base
- Halogen
- Alkyl Halide
- Aldehyde or Ketones (ALDOL)
- Esterification
- Fischer Esterification
- Ester hydrolysis (saponification)
- Acid Chlorides
- Andydrides
Looks like I have a lot ahead of me before friday

Comments (0)