An organic compound with the molecular formula C9H10O forms 2, 4-DNP derivative, reduces Tollens’ reagent and undergoes Cannizzaro reaction. On vigorous oxidation, it gives 1, 2-benzenedicarboxylic | Shaalaa.com

Vilsmeier-Haack Reaction | NROChemistry

Organic Reaction Hub on Instagram: "In 1925, A. Vilsmeier et al. reported that upon treatment with POCl3, N-methylacetanilide give 4-chloro-1,2-dimethylquinolinium chloride as major product. Most often the reaction of DMF and POCl3 result Vilsmeier reagent (weak electrophile), which readily reacts with electron-rich aromatic compounds afford formylated product. Reaction conditions: Solvent is usually a halogenated hydrocarbon, DMF or POCl3 & temperature from 0 °C up to 80 °C. Mechanism: Formatio

Complete synthesis by giving missing starting material, reagent or product. →[(i) O3][(ii) Zn-H2O] 2 O | Shaalaa.com

Synthesis of benzoic acid from Grignard reagent | Chemistry Online