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Toluene (/ ˈtɒl.juiːn /), also known as toluol (/ ˈtɒl.ju.ɒl, - ɔːl, - oʊl /), is a substituted aromatic hydrocarbon [15] with the chemical formula C6H5CH3, often abbreviated as PhCH3, where Ph stands for phenyl group. It is a colorless, water -insoluble liquid with the odor associated with paint thinners.
Toluene is a clear, colorless liquid with a distinctive smell. Toluene occurs naturally in crude oil and in the tolu tree. It is also produced in the process of making gasoline and other fuels from crude oil and making coke from coal.
17 Σεπ 2024 · Toluene has a simple and distinctive structure consisting of a benzene ring bonded to a single methyl group (CH₃). This means that six carbon atoms form a hexagonal ring with alternating double bonds, while one carbon of this ring is attached to a group of three hydrogen atoms.
Toluene is a clear, colourless liquid with a benzene-like odour. The chemical formula of toluene can be written as C 6 H 5 CH 3. Toluene is a naturally occurring compound derived primarily from petroleum or petrochemical processes. Toluene is a common component in gasoline, glues, and paint products.
11 Οκτ 2024 · Toluene, aromatic hydrocarbon used extensively as starting material for the manufacture of industrial chemicals. It comprises 15–20 percent of coal-tar light oil and is a minor constituent of petroleum. Both sources provide toluene for commercial use, but larger amounts are made by catalytic.
Toluene is a hydrocarbon, specifically an aromatic hydrocarbon, with the chemical formula C 7 H 8 or CH 3 C 6 H 5. Its structure consists of a methyl group (CH 3) attached to a phenyl group (C 6 H 5), which is a cyclic ring of six carbon atoms.
Toluene. Chemical structure: This structure is also available as a 2d Mol file or as a computed 3d SD file The 3d structure may be viewed using Java or Javascript. Permanent link for this species. Use this link for bookmarking this species for future reference.
