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Pentan-3-ol. Other names 3-Pentanol, diethyl carbinol ... 3-Pentanol is one of the eight isomers of amyl alcohol. It is found naturally and has a role as a pheromone ...
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 .
Isoamyl alcohol is a colorless liquid with the formula C 5 H 12 O, specifically (H 3 C–) 2 CH–CH 2 –CH 2 –OH. It is one of several isomers of amyl alcohol (pentanol). It is also known as isopentyl alcohol, isopentanol, or (in the IUPAC recommended nomenclature) 3-methyl-butan-1-ol.
2-Pentanol (IUPAC name: pentan-2-ol; also called sec-amyl alcohol) is an organic chemical compound.It is used as a solvent and an intermediate in the manufacturing of other chemicals. 2-Pentanol is a component of many mixtures of amyl alcohols sold industrially. 2-Pentanol is chiral and thus can be obtained as either of two stereoisomers designated as (R)-(−)-2-pentanol and (S)-(+)-2-pentanol.
1-Pentanol, (or n-pentanol, pentan-1-ol), is an organic compound with the formula CH 3 CH 2 CH 2 CH 2 CH 2 OH and is classified as a primary alcohol. [2] It is a colourless liquid with a distinctive aroma. It is one of 8 isomeric alcohols with the formula C 5 H 11 OH. It is used as a solvent, a biological drying agent and in the synthesis of ...
3-Methyl-3-pentanol: 6 carbon atoms: branched: C 6 H 14 O 1-Heptanol (enanthic alcohol) 7 carbon atoms: C 7 H 16 O 1-Octanol (capryl alcohol) 8 carbon atoms: C 8 H 18 O Pelargonic alcohol (1-nonanol) 9 carbon atoms: C 9 H 20 O 1-Decanol (decyl alcohol, capric alcohol) 10 carbon atoms: C 10 H 22 O Undecyl alcohol (1-undecanol, undecanol ...
Neopentyl alcohol can be prepared from the hydroperoxide of diisobutylene. [3] It can also be prepared by the reduction of trimethylacetic acid with lithium aluminium hydride . Neopentyl alcohol was the first described in 1891 by L. Tissier, who prepared it by reduction of a mixture of trimethyl acetic acid and trimethylacetyl chloride with ...
An example is the pair propanal H 3 C–CH 2 –C(=O)-H and acetone H 3 C–C(=O)–CH 3: the first has a –C(=O)H functional group, which makes it an aldehyde, whereas the second has a C–C(=O)–C group, that makes it a ketone. Another example is the pair ethanol H 3 C–CH 2 –OH (an alcohol) and dimethyl ether H 3 C–O–CH 2 H (an ether).