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The word's meaning became restricted to "spirit of wine" (the chemical known today as ethanol) in the 18th century and was extended to the class of substances so-called as "alcohols" in modern chemistry after 1850. [16] The term ethanol was invented in 1892, blending "ethane" with the "-ol" ending of "alcohol", which was generalized as a libfix ...
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Pages in category "Alcohol solvents" The following 29 pages are in this category, out of 29 total. This list may not reflect recent changes. A. Tert-Amyl alcohol; B.
See alcohol (chemistry) for description. Subcategories. This category has the following 12 subcategories, out of 12 total. A. Acyloins (11 P) C. Cyclohexenols (1 C ...
To be alcohol, the -OH must be bonded to a carbon. Use the suffix -ol to denote which carbon the alcohol group is on. A three-carbon chain with the -OH on the second carbon would be propan-2-ol. Note that in some instances, common names are better. If the -OH is on the end of the chain, or the carbon chain is only 1 or 2, use no number.
This category is about alcohol as it pertains to organic chemistry. For more information on human consumption of ethanol , see Category:Alcohol and Category:Alcoholic drinks . Pages in this category should be moved to subcategories where applicable.
Allyl alcohol (IUPAC name: prop-2-en-1-ol) is an organic compound with the structural formula CH 2 =CHCH 2 OH. Like many alcohols, it is a water-soluble, colourless liquid. It is more toxic than typical small alcohols. Allyl alcohol is used as a precursor to many specialized compounds such as flame-resistant materials, drying oils, and ...
Geminal diols are a subclass of the diols, which in turn are a special class of alcohols. Most of the geminal diols are considered unstable. The simplest geminal diol is methanediol CH 4 O 2 or H 2 C(OH) 2. Other examples are: dihydroxymalonic acid (HOOC) 2 C(OH) 2; decahydroxycyclopentane (C(OH) 2) 5; chloral hydrate (Cl 3 C)HC(OH) 2.