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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 ...
2,3-Dimethylpentane; 2,4-Dimethylpentane; 3,3-Dimethylpentane This page was last edited on 17 March 2021, at 16:47 (UTC). Text is available under the Creative ...
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.
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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.
3-Methylhexane is a branched hydrocarbon with two enantiomers. [2] It is one of the isomers of heptane. The molecule is chiral, and is one of the two isomers of heptane to have this property, the other being its structural isomer 2,3-dimethylpentane. The enantiomers are (R)-3-methylhexane [3] and (S)-3-methylhexane. [4]
2,3,3-Trimethylpentane is a chemical compound in the family of hydrocarbons which has a formula of C 8 H 18. It is an isomer of octane . It has a role as a human metabolite, a bacterial metabolite and a mammalian metabolite. [ 2 ]
Skeletal formula of 2,3,4-trimethylpentane with some implicit hydrogens added: Names Preferred IUPAC name. ... 2,3,4-Trimethylpentane is a branched alkane.