University:
Binghamton University
Course:
CHEM 231 | Organic Chemistry I
Academic year:

2024
Views:

109

Pages:

2
Author:

CrystalMintah

**1.1.1. Cannizzaro Disproportionation** [Image of a chemical reaction: 2 Benzaldehyde + KOH -> Benzyl alcohol + Potassium benzoate] **1.1.2. Alpha Oxidation** [Image of a chemical reaction involving the oxidation of an alpha hydrogen] **1.1.3. Haloform Reaction** [Image of a chemical reaction involving the halogenation of a methyl ketone] **1.2.1. Aldol Condensation** [Image of an aldol condensation reaction] **1.2.2. Claisen Condensation** [Image of a Claisen condensation reaction] **1.2.3. Perkin Reaction** [Image of a Perkin reaction] **1.3.1. Aldol Addition** [Image of an aldol addition reaction] **1.3.2. Michael Addition** [Image of a Michael addition reaction] **1.3.3. Grignard Reaction** [Image of a Grignard reaction] **1.3.4. Wittig Reaction** [Image of a Wittig reaction] **1.3.5. Dieckmann Condensation** [Image of a Dieckmann condensation reaction] **1.3.6. Darzen's Glycidic Ester Condensation** [Image of a Darzen's Glycidic Ester Condensation reaction] **1.3.7. Benzoin Condensation** [Image of a Benzoin condensation reaction] **Key Notes on Mechanism** **Michael Addition:** [Image of a Michael addition reaction mechanism] * Nucleophile must have alpha-hydrogen * Product consists of an α,β-unsaturated carbonyl compound (enone) and a nucleophile (carbon or oxygen nucleophile) * Reaction is reversible **Aldol Addition/Condensation:** [Image of an aldol addition/condensation reaction]