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Chemical formula. C 8 H 18: Molar mass: 114.232 g·mol −1 Appearance Colourless liquid Odor: ... 2,3-Dimethylhexane is a structural isomer of octane. References
3,4-Dimethylhexane [Wikidata Index of chemical compounds with the same name This set index article lists chemical compounds articles associated with the same name.
3-Methyl-3-pentanol (IUPAC name: 3-methylpentan-3-ol) is an organic chemical compound and a tertiary hexanol. It is used in the synthesis of the tranquilizer emylcamate , [ 2 ] and has similar sedative and anticonvulsant actions itself.
The molecular formula C 6 H 14 O may refer to: tert-Amyl methyl ether; Diisopropyl ether; Dimethylbutanols. 2,2-Dimethyl-1-butanol; 3,3-Dimethyl-1-butanol; Dipropyl ether; 2-Ethyl-1-butanol; Ethyl tert-butyl ether; Hexanols. 1-Hexanol; 2-Hexanol; 3-Hexanol; Methylpentanols. 2-Methyl-1-pentanol; 3-Methyl-1-pentanol; 4-Methyl-1-pentanol; 2-Methyl ...
In contrast, a secondary alcohol has a formula “–CHROH” and a tertiary alcohol has a formula “–CR 2 OH”, where “R” indicates a carbon-containing group. Examples of primary alcohols include ethanol and 1-butanol. Methanol is also generally regarded as a primary alcohol, [2] [3] including by the 1911 edition of the Encyclopædia ...
For example, C(CH 3) 4 (neopentane) is named 2,2-dimethylpropane. If there are different groups, they are added in alphabetical order, separated by commas or hyphens. The longest possible main alkane chain is used; therefore 3-ethyl-4-methylhexane instead of 2,3-diethylpentane, even though these describe equivalent structures.
Hexanol may refer to any of the following isomeric organic compounds with the formula C 6 H 13 OH: Structure Type ... 2,3-Dimethylbutan-2-ol: 119
Butanol (also called butyl alcohol) is a four-carbon alcohol with a formula of C 4 H 9 O H, which occurs in five isomeric structures (four structural isomers), from a straight-chain primary alcohol to a branched-chain tertiary alcohol; [1] all are a butyl or isobutyl group linked to a hydroxyl group (sometimes represented as BuOH, sec-BuOH, i-BuOH, and t-BuOH).