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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.
Where an acid has both a systematic and a common name (like CH 3 COOH, for example, which is known as both acetic acid and as ethanoic acid), its salts can be named from either parent name. Thus, KCH 3 CO 2 can be named as potassium acetate or as potassium ethanoate. The prefix form, is "carboxylato-".
Dimethylpentane may refer to: 2,2-Dimethylpentane; 2,3-Dimethylpentane; 2,4-Dimethylpentane; 3,3-Dimethylpentane This page was last edited on 17 March ...
Like typical alkanes, it is a colorless flammable compound; under common ambient conditions, it is a mobile liquid, less dense than water. [1] 2,3-Dimethylpentane is notable for being one of the two simplest alkanes with optical (enantiomeric) isomerism.
3-Methylpentane is a branched alkane with the molecular formula C 6 H 14. It is a structural isomer of hexane composed of a methyl group bonded to the third carbon atom in a pentane chain. It is of similar structure to the isomeric 2-methylpentane , which has the methyl group located on the second carbon of the pentane chain.
3,3-Dimethylpentane; 3-Ethylpentane; Heptane; Methylhexanes. 2-Methylhexane; 3-Methylhexane; 2,2,3-Trimethylbutane This page was last edited on 14 October 2020, at ...
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The main structure of chemical names according to IUPAC nomenclature. The International Union of Pure and Applied Chemistry (IUPAC) has published four sets of rules to standardize chemical nomenclature. There are two main areas: IUPAC nomenclature of inorganic chemistry (Red Book) IUPAC nomenclature of organic chemistry (Blue Book)