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Triphenylmethanol (also known as triphenylcarbinol and TrOH) is an organic compound. It is a white crystalline solid that is insoluble in water and petroleum ether, but well soluble in ethanol, diethyl ether, and benzene. In strongly acidic solutions, it produces an intensely yellow color, due to the formation of a stable "trityl" carbocation ...
Triphenylmethane or triphenyl methane (sometimes also known as Tritan), is the hydrocarbon with the formula (C 6 H 5) 3 CH. This colorless solid is soluble in nonpolar organic solvents and not in water.
(E)-Stilbene, commonly known as trans-stilbene, is an organic compound represented by the condensed structural formula C 6 H 5 CH=CHC 6 H 5.Classified as a diarylethene, it features a central ethylene moiety with one phenyl group substituent on each end of the carbon–carbon double bond.
Hydrogen in an electrical discharge tube. Hydrogen is a colourless, odourless, and comparatively unreactive diatomic gas with a density of 8.988 × 10 −5 g/cm 3 and is about 14 times lighter than air. It condenses to a colourless liquid −252.879 °C and freezes into an ice- or snow-like solid at −259.16 °C.
Organotin compounds are those with tin linked to hydrocarbons. The compound on the picture is trimethyltin chloride, an example of organotin compounds.. Organotin chemistry is the scientific study of the synthesis and properties of organotin compounds or stannanes, which are organometallic compounds containing tin–carbon bonds.
white Density: 1.308 g/cm 3 [2] ... It is a white or colorless solid. ... triphenylene has attracted attention as the core of discotic mesogen in liquid crystalline ...
At room temperature it appears as a colorless crystalline solid, with monoclinic structure. It is well miscible in diethyl ether and benzene, but it is practically insoluble in water, and partially in ethanol. Its derivatives have useful properties in electrical conductivity and electroluminescence, and they are used in OLEDs as hole ...
Triphenylmethyl chloride is commercially available. It may be prepared by the reaction of triphenylmethanol with acetyl chloride, or by the Friedel–Crafts alkylation of benzene with carbon tetrachloride to give the trityl chloride-aluminium chloride adduct, which is then hydrolyzed. [3]