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Kameton Org.Chem.StudyWithMe. @UC8Xq58mKsBJAlpNq9ElzMSA@youtube.com

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Thanks for coming to see my #shorts . Let's study organic ch

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[SN1] The Mechanism for an SN1 Reaction [SN2] Williamson ether synthesis Diels-Alder Reaction Alkylation using a ACETYLIDE ion. Hydroboration and Oxymercuration of Alkynes Alkylating the α-carbon using an Enamine. Halogenation of the α-carbon of Ketone Reactions of Alkyne Ozonolysis of Alkenes Epoxidation: Addition of a peroxyacid to alkene Halogen Addition to Alkenes 2: Halohydrin formation Halogen Addition to Alkenes 1: In cyclic bromonium ion is cation rearrangement possible? Alcohol synthesis from Alkenes: Markovnikov’s rule and Hydroboration–Oxidation Mannich Reaction Synthesis of Aspirin: via Kolbe–Schmitt carboxylation reaction. [Stork reaction] Michael reaction using Enamines. Suzuki Reaction Alkylation of benzene by Wolff-Kishner reduction [Re-upload] Friedel-Crafts Alkylation Reaction of Benzene with hydride shift Gattermann–Koch reaction Friedel–crafts acylation of benzene: Reaction of carbon cations with aromatic rings Sulfonation of benzene Nitration of benzene Aniline to Iodobenzene: Synthesis of iodobenzene via diazonium salt Halogenation of benzene: Mechanism for bromination Decarboxylation 2: How prepare 4-methyl-3-heptanone, starting with methyl propanoate? Decarboxylation 1: Synthesis of a carboxylic acid using diethyl malonate as the starting material. DDT :It found to be highly toxic to insects and relatively less toxic to animals but
 Alkylating the Unsymmetrical ketones. Which is the major product ? Robinson annulation: A Michael reaction followed by an intramolecular aldol condensation. Dieckmann Condensation: An intramolecular Claisen condensation. Claisen Condensation: Two esters containing α-hydrogens, promoted by the base, affords ÎČ-ketoesters Claisen-Schmidt Condensation: A method for obtaining one product from cross aldol addition Aldol condensation: Reaction proceeds via E1cB to give a conjugated enone. Aldol addition: Connecting the α-carbon of one with the carbonyl carbon of the other. [Michael reaction] A conjugate addition reaction with carbanion nucleophile. Alkylating the α-carbon via enolate formation [HVZ reaction] Halogenation a carboxylic acid at the α-carbon. Ether synthesis from 4-hydroxybenzoic acid