Aldehyde and Ketone Flashcards
Two ways to prepare aldehydes
- Oxidation of primary Alcohol
- Partial Reduction with DIBAH
Primary Alcohol React with DMP
Alcohol turns into aldehyde
Partial Reduction with DIBAH to make aldehyde
Reactant: DIBAH
Reagent: Ester
Result: Alcohol + Aldehyde
Secondary Alcohol React with DMP
Alcohol turns into ketone
What happen when alkene under ozonolysis?
Alkene is cleave to form C=O
Reagent
1. O3
2. Zn/H3O+
Preparing Ketone from Aromatic Rings
Fridel Craft Acylation
Reagent: RCO-Cl / AlCl3
Oxidation of Aldehyde
Aldehyde to Carboxylic Acid
Reagent: CrO3, KmnO4, Na2Cr2O7
Grignard Reagent on Aldehyde and Ketone
Reagent: MgX-R / H3O+
Double Bonded O turn into Alcohol
Central Carbon is bonded to R
Cyanohydrin Formation on Aldehyde and Ketone
Double Bond O turns into Alcohol
Central Carbon is bonded to CN
Reagent: HCN, H2O / OH
Hydration of Aldehyde and Ketone
Geminial diol is formed
Reagent: H3O+ or -OH/H2O
Woff Kishmer Reaction2
Converting Aldehyde or Ketone into Alkane
Formation of Iminine
- Nucleophilic Attack
- Protonation of Oxygen
- Deprotonation of Nitrogen
- Protonation of Oxygen to form Water
- Elimination of Water
- Deprotonation of Nitrogen to form Iminine
Formation of Enamine
- Protonation of Oxygen
- Nucleophilic Attack
- Deprotonation of Nitrogen
- Protonation of Oxygen to form Water
- Elimation of Water
- Deprotonation of Alpha proton