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Heat phenol hydrogenation

C, b.p. 16UC. Manufactured by heating phenol with hydrogen under pressure in the presence of suitable catalysts. Oxidized to adipic acid (main use as intermediate for nylon production) dehydrogenated to cyclohexanone. [Pg.122]

Dienes, 11 addition to, 194-198 cisoid conformation, 197, 350 conjugated, 11 Cope rearrangement, 354 cycUsation, 346 cycloaddition to, 348 Diels-Alder reaction, 197, 349 excited state, 13 heat of hydrogenation, 16,194 isolated, 11 m.o.s of, 12 polymerisation, 323 Dienone intermediates, 356 Dienone/phenol rearrangement, 115 Dienophiles, 198, 350 Digonal hybridisation, 5 Dimedone, 202 Dimroth s Et parameter, 391 solvatochromic shifts, 391 solvent polarity, 391 Y and,392 Dinitrofluorobenzene proteins and, 172... [Pg.208]

The main reservoir of chemicals available to the nineteenth century chemists was coal. Distillation of coal to give gas for lighting and heating (mainly hydrogen and carbon monoxide) also gave a brown tar rich in aromatic compounds such as benzene, pyridine, phenol, aniline, and thiophene. [Pg.3]

Now heat the tube very gently at first and then more strongly. A non-conden-sible product such as hydrogen or methane is best detected by collecting a sample of the gas in a test-tube as shown in Fig. 71(A). A condensible product such as benzene or phenol should be collected by twisting the delivery-tube downwards and collecting the liquid in a few ml. of water in a test-tube as shown In Fig. 71(B). [Pg.327]

Dimethyl sulphate is of particular value for the methylation of phenols and sugars. The phenol is dissolved in a slight excess of sodium hydroxide solution, the theoretical quantity of dimethyl sulphate is added, and the mixture is heated on a water bath and shaken or stirred mechanically (compare Section IV, 104). Under these conditions only one of the methyl groups is utilised the methyl hydrogen sulphate formed in the reaction reacts with the alkali present. -... [Pg.303]

Heat 0 5 g. of pseudo-saccharin chloride with an excess of the phenol to 125-140° for 15-20 minutes hydrogen chloride is evolved. Wash the product with dilute sodium hydroxide solution and then with water. Recrystallise the derivative from ethanol. [Pg.684]


See other pages where Heat phenol hydrogenation is mentioned: [Pg.80]    [Pg.446]    [Pg.449]    [Pg.117]    [Pg.174]    [Pg.156]    [Pg.171]    [Pg.32]    [Pg.404]    [Pg.415]    [Pg.415]    [Pg.1043]    [Pg.1044]    [Pg.1045]    [Pg.300]    [Pg.108]    [Pg.108]    [Pg.177]    [Pg.477]    [Pg.541]    [Pg.19]    [Pg.784]    [Pg.854]    [Pg.1038]    [Pg.314]    [Pg.278]    [Pg.294]    [Pg.66]    [Pg.68]    [Pg.342]    [Pg.224]    [Pg.227]    [Pg.218]    [Pg.609]    [Pg.723]    [Pg.220]   
See also in sourсe #XX -- [ Pg.146 ]




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Hydrogen heats

Hydrogen phenol hydrogenation

Phenols hydrogenation

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