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2-Methyl-3-pentanol (IUPAC name: 2-methylpentan-3-ol) is an organic chemical compound. It is a secondary alcohol [2] that is used as a fuel. [3] References
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.
2-Methyl-3-pentanol; 3-Methyl-3-pentanol This page was last edited on 17 January 2021, at 03:03 (UTC). Text is available under the Creative Commons Attribution ...
Three of these alcohols, 2-methyl-1-butanol, 2-pentanol, and 3-methyl-2-butanol (methyl isopropyl carbinol), contain stereocenters, and are therefore chiral and optically active. The most important amyl alcohol is isoamyl alcohol , the chief one generated by fermentation in the production of alcoholic beverages and a constituent of fusel oil .
2-Methyl-3-pentanol; 3-Methyl-3-pentanol; 2,2-Dimethyl-1-butanol; 2,3-Dimethyl-1-butanol; 3,3-Dimethyl-1-butanol This page was last edited on 27 ...
2-Methyl-2-pentanol (IUPAC name: 2-methylpentan-2-ol) is an organic chemical compound. It can be added to a gas chromatograph to help distinguish between branched compounds, especially alcohols. [2] Its presence in urine can be used to test for exposure to 2-methylpentane. [3]
The conversion of ethanol to ethylene is a fundamental example: [3] [4] CH 3 CH 2 OH → H 2 C=CH 2 + H 2 O. The reaction is accelerated by acid catalysts such as sulfuric acid and certain zeolites. These reactions often proceed via carbocation intermediates as shown for the dehydration of cyclohexanol. [5] Some alcohols are prone to dehydration.
When necessary, the position of the hydroxyl group is indicated by a number between the alkane name and the -ol: propan-1-ol for CH 3 CH 2 CH 2 OH, propan-2-ol for CH 3 CH(OH)CH 3. If a higher priority group is present (such as an aldehyde , ketone , or carboxylic acid ), then the prefix hydroxy- is used, [ 19 ] e.g., as in 1-hydroxy-2 ...