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The Piria reaction. In the Tyrer sulfonation process (1917), [7] at some time of technological importance, benzene vapor is led through a vessel containing 90% sulfuric acid the temperature of which is increased from 100 to 180°C. Water and benzene are continuously removed and the benzene fed back to the vessel. In this way an 80% yield is ...
For example, reaction of aniline with sulfuric acid at 180 °C produces sulfanilic acid, H 2 NC 6 H 4 SO 3 H. If bromine water is added to aniline, the bromine water is decolourised and a white precipitate of 2,4,6-tribromoaniline is formed. To generate the mono-substituted product, a protection with acetyl chloride is required:
The Hinsberg reaction is a chemical test for the detection of primary, secondary and tertiary amines. The reaction was first described by Oscar Hinsberg in 1890. [ 1 ] [ 2 ] In this test, the amine is shaken well with the Hinsberg reagent ( benzenesulfonyl chloride ) in the presence of aqueous alkali (either KOH or NaOH).
The hydrochloric acid and sodium hydroxide byproducts undergo a secondary reaction to release the byproducts of water and sodium chloride. The overall reaction is thus NaOCl + 2NH 3 → N 2 H 4 + NaCl + H 2 O. Excess ammonia and sodium chloride are removed by distillation, followed by azeotropic distillation with aniline to remove water.
2,4,6-Trichloroaniline can be prepared by reaction of dry aniline with chlorine gas while in an anhydrous solution of carbon tetrachloride. 2,4,6-Trichloroaniline precipitates from solution as a white solid. In the presence of water in the solution the white material will be contaminated with aniline black. [3]
In the context of a chemical reaction the term neutralization is used for a reaction between an acid and a base or alkali. Historically, this reaction was represented as acid + base (alkali) → salt + water x H y A + y B(OH) x → B y A x + xy H 2 O. For example: HCl + NaOH → NaCl + H 2 O
The sodium fusion extract is made alkaline by adding NaOH. To this mixture, freshly prepared FeSO 4 solution is added and boiled for some time and then cooled. A few drops of FeCl 3 are added and Prussian blue (bluish green) color forms due to formation of ferric ferrocyanide along with NaCl. This shows the presence of nitrogen in the organic ...
The reaction of anthracene with N-methylformanilide, also using phosphorus oxychloride, gives 9-anthracenecarboxaldehyde: N -Methylformanilide and anthracene and phosphorus oxychloride In general, the electron-rich arene ( 3 ) must be much more active than benzene for the reaction to proceed; phenols or anilines are good substrates.