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As of early 1990s, it was present in American [4] and European [5] gasoline in small amounts, and by 2011 its share in US gas varied between 2 and 8%. [6] Using a quantitative structure-activity relationship (QSAR) prediction model, 2-Methylpentane has a research octane number (RON) of 75, motor octane number (MON) of 77, and cetane number (CN ...
This compound is known as 2,3,3-trimethylpentane. Here three identical alkyl groups attached to carbon atoms 2, 3, and 3. Here three identical alkyl groups attached to carbon atoms 2, 3, and 3. The numbers are included in the name to avoid ambiguity about the position of the groups, and "tri" indicates that there are three identical methyl groups.
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-Ethylpentane (C 7 H 16) is a branched saturated hydrocarbon. It is an alkane, and one of the many structural isomers of heptane, consisting of a five carbon chain with a two carbon branch at the middle carbon. An example of an alcohol derived from 3-ethylpentane is the tertiary alcohol 3-ethylpentan-3-ol. [3]
Methylpentane may refer to: 2-Methylpentane; 3-Methylpentane; You could also have been looking for: Methylpentenone This page was last edited on 2 April 2021 ...
The optical center is the middle carbon of the pentane backbone, which is connected to one hydrogen atom, one methyl group, one ethyl group – C 2 H 5, and one isopropyl group – CH(CH 3) 2. The two enantiomers are denoted (3R)-2,3-dimethylpentane and (3S)-2,3-dimethylpentane (the other simplest chiral alkane is its structural isomer 3 ...
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At –75 °C, the product ratio is 48:35:17 mixture of n-hexane, 2-methylpentane, and 3-methylpentane. The ratio is remarkably close to the statistical product ratio of 6:4:2 (~50:33:17) based on the number of available C–H bonds at each position that could undergo methylene insertion. As a result, Doering and coworkers concluded: