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Phenol hydrogenation tests

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]

VALGiMiGLi L, BANKS J T, INGOLD K u and LuszTYK J (1995) Kiuetic solveut effects on hydroxylic hydrogen atom abstractions are independent of the nature of the abstrarting radical. Two extreme tests using vitamin E and phenol, J Am Chem Soc, 117, 9966-71. [Pg.345]

In the work now reported coal fractions derived from a solubilised coal were reacted individually with Tetralin, without any additions of catalyst or gaseous hydrogen, and the reaction products studied to determine the effect that chemical type had on the reaction. The untreated whole coal was also reacted to test whether phenol, present in the coal fractions as a result of the fractionation procedure, was having any significant effect on the reaction with the fractions. [Pg.242]

Several preparation methods have been reported for the synthesis of TS-1. In this work, we have investigated the physicochemical properties of TS-1 samples synthesized by different preparation metiiods and tested these materials as catalysts for the oxidation of n-octane, 1-hexene and phenol using aqueous hydrogen peroxide (30 wt%) as oxidant at temperatures below 100 C. For comparison, Ti02 (anatase) and the octahedral titanium-containing silicate molecular sieve (ETS-10) (5) have been studied. The effect of the presence of aluminum and/or sodium on the catalytic activity of TS-1 is also discussed. [Pg.273]

They react with a solution of bromine in carbon tetrachloride by sub stitution and an equivalent quantity of hydrogen bromide is evolved (compare addition with unsaturated compounds). When the test is conducted with bromine water and a dilute aqueous solution of a phenol, the sign of reaction is the separation of a sparingly soluble bromine substitution product. ... [Pg.1071]


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