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9 – MgBr with acetone to form 2,3-dimethyl-2-pentanol, then dehydrating this alcohol to form 2,3-dimethyl-2-pentene, and hydrogenating this product. [ 4 ] The isomer is present at about 2.4% by weight in the hydrocarbon mixture obtained by the condensation of methanol at 200 °C with a zinc iodide catalyst (the main component of the mixture ...
2,2-Dimethylpentane can form a clathrate hydrate with helper gas molecules. The type of clathrate formed is called "clathrate H". 2,2-Dimethylpentane was the first compound for which the structure was determined. The clathrate has 34 molecules of water per molecule, and also has xenon and hydrogen sulfide as helper molecules.
2,4-Dimethylpentane is an alkane with the chemical formula [(H 3 C) 2 CH] 2 CH 2. This colorless hydrocarbon is produced in large quantities in oil refineries. It results from the alkylation of isobutane by propylene. [1] Often referred to as "alkylate", it is blended with other gasoline components to give a high octane fuel.
In 1929 Graham Edgar and George Calingaert made 3,3-dimethylpentane and measured its physical characteristics for the first time. The measurements were at 20 °C, not the standard conditions used in later times. [3] For 3,3-dimethylpentane they measured a density of 0.6934 at 20 °C with a rate of change Δd/ΔT of 0.000848.
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3-Methylheptane is a branched alkane isomeric to octane. Its structural formula is CH 3 CH 2 CH(CH 3)CH 2 CH 2 CH 2 CH 3. It has one stereocenter. Its refractive index is 1.398 (20 °C, D). [citation needed]
The 3 substrates of this enzyme are dodecanoyl-CoA, H 2 O, and 2-oxoglutarate, whereas its two products are (3S,4S)-3-hydroxytetradecane-1,3,4-tricarboxylate and CoA. This enzyme belongs to the family of transferases, specifically those acyltransferases that convert acyl groups into alkyl groups on transfer. The systematic name of this enzyme ...