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Browse all Organic Chemistry II Key Terms

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[1,3] sigmatropic rearrangement
[3,3] sigmatropic rearrangement
[4+2] cycloaddition
α,β-unsaturated carbonyl compound
α,β-unsaturated carbonyls
α-anomer
α-enolate
α-glycosidic bond
β-anomer
β-enolate
β-glycosidic bond
β-hydroxy carbonyl compound
β-keto ester
β-keto esters
γ-butyrolactone
δ-valerolactone
1,3-dipolar cycloaddition
1,3-hexadiene
1,5 Sigmatropic Rearrangement
1,7 sigmatropic rearrangement
13C NMR
1H NMR
2+2 cycloaddition
2,4-dinitrophenylhydrazine
2,4-hexadiene
2,4-pentanedione
2-lithiopyridine
4n+2 rule

A

Absorbance
Absorption spectrum
Accurate Mass Measurement
Acetal Formation
Acetamide
Acetic Acid
Acetic anhydride
Acetyl-CoA
Acetylation
Acetylbenzoic anhydride
Acetylsalicylic acid
Acid Catalysts
Acid Chloride
Acid-Base Reactions
Acid-catalyzed hydrolysis
Acid-catalyzed tautomerization
Acidic amino acids
Acidic Conditions
Acidity
Activating Groups
Activation Energy
Activation Energy Considerations
Active site
Acyclic terpenes
Acyl chloride
Acylation
Acylation of Amines
Acylium ion intermediate
Acyltransferase
Addition Product
Addition-elimination mechanism
Adp-glucose
Advantages over hydrogenation
Agricultural chemicals
Alcohol
Alcohol protection
Alcohols
Aldehyde
Aldehyde functional group
Aldehydes
Aldol Condensation
Aldol disconnections
Aldol Reaction
Aldose
Aliphatic amines
Aliphatic Amino Acids
Alkene group