20 0 obj 38 0 obj The methyl group of toluene is a side chain in the aromatic ring structure and is oxidized to the carboxyl group in the presence of a strong oxidizing agent. 41 0 obj
Reactions of toluene.
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The needles form there and fall. endobj • Moreover, it is used as a precursor of the reaction of substitution and oxidation to perform ready-to-use products or another precursor. <>/Subtype/Link/C[0 0 1]/Border[0 0 0]/Rect[306.83 639 335.49 648]>> If the mixture is heated again, the crystals will dissolve and the experiment can be repeated. Full conversion of the starting materials could not be achieved even after 24 h stirring. <>/Subtype/Link/C[0 0 1]/Border[0 0 0]/Rect[235.23 691 262.49 700]>> Toluene is flammable so don't use a gas stove or Bunsen burner. <>/Subtype/Link/C[0 0 1]/Border[0 0 0]/Rect[432.67 119 459.83 128]>> Its IUPAC systematic name is methylbenzene.
• Additionally, toluene has been shown to display antidepressant-like effects in rodents in the forced swim test (FST) and the tail suspension test (TST), likely due to its NMDA antagonist properties. What do they do with the flask after that? • Toluene is needed for dinitrotoluene, which is required for toluene diisocyanate, which is used to produce polyurethane foams. endobj endobj
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Alkanes won’t react with KMnO 4. 17 0 obj
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