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A more common structural isomer of this compound is cumene. n-Propylbenzene is used as a nonpolar organic solvent in various industries, including printing and the dyeing of textiles and in the manufacture of methylstyrene. [1] [2] It can be synthesized by the reaction of the Grignard reagent derived from benzyl chloride with diethyl sulfate. [3]
trans-Propenylbenzene is an organic compound with the formula C 6 H 5 CH=CHCH 3. It is the more stable [ 2 ] of the two isomers of 1-propenylbenzene. Both isomers are colorless flammable liquids.
n-Propylbenzene, the straight chain isomer (IUPAC name propylbenzene) Cumene (isopropylbenzene) This page was last edited on 20 May 2021, at ...
For the hydrocarbons with no further unsaturation, there are four isomers. The chemical formula for all the saturated isomers is C 9 H 12. There are three trimethylbenzenes, three ethylmetylbenzenes, and two propylbenzene isomers. 1980s American gasoline contained about 3-4% C 3-benzenes. [1]
Phenylpropene specifically may refer to the following isomers of C 9 H 10 (molar mass 118.179 g/mol): trans-Propenylbenzene (trans-1-phenylpropene) α-Methylstyrene (2-phenylpropene) Allylbenzene (3-phenylpropene)
In organic chemistry, 1-propenyl (or simply propenyl) has the formula CH=CHCH 3 and 2-propenyl (isopropenyl) has the formula CH 2 =C-CH 3. These groups are found in many compounds. These groups are found in many compounds.
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In addition to p-cymene, two less common geometric isomers are o-cymene, in which the alkyl groups are ortho-substituted, and m-cymene, in which they are meta-substituted. p-Cymene is the only natural isomer, as expected from the terpene rule. All three isomers form the group of cymenes. Cymene is also produced by alkylation of toluene with ...