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Dimethylbutene is an alkene with a molecular formula C 6 H 12. It has the following possible structural isomers: 2,3-Dimethyl-1-butene; 3,3-Dimethyl-1-butene;
Like the other isomers of dimethylbutene, it is a colorless liquid. Together with 2,3-dimethyl-2-butene it can be produced by dimerization of propylene. It is a precursor to the commercial fragrance tonalide. [1]
Alkenes are hydrocarbons that have one or more double bonds between carbon atoms. Subcategories This category has the following 11 subcategories, out of 11 total.
This page was last edited on 28 November 2024, at 15:29 (UTC).; Text is available under the Creative Commons Attribution-ShareAlike 4.0 License; additional terms may apply.
Dimethylbutadiene readily undergoes Diels-Alder reactions and reacts faster than 1,3-butadiene.Its effectiveness in this reaction is attributed to the stabilization of the cis-conformation owing to the influence of the methyl groups on the C2 and C3 positions.
The ozonolysis of alkenes is sometimes referred to as "Harries ozonolysis", because some attribute this reaction to Carl Dietrich Harries. [16] Before the advent of modern spectroscopic techniques, the ozonolysis was an important method for determining the structure of organic molecules.
This page was last edited on 26 December 2021, at 22:00 (UTC).; Text is available under the Creative Commons Attribution-ShareAlike 4.0 License; additional terms may apply.
2-Methyl-2-butene, 2m2b, 2-methylbut-2-ene, beta-isoamylene, or Trimmethylethylene is an alkene hydrocarbon with the molecular formula C 5 H 10. Used as a free radical scavenger in trichloromethane (chloroform) and dichloromethane (methylene chloride). It is also used to scavenge hypochlorous acid (HOCl) in the Pinnick oxidation.