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Fluoroalcohol. 3 languages. 日本語 ... Stable perfluorinated alcohols include nonafluoro-tert-butyl alcohol ((CF 3) 3 COH) and pentafluorophenol (C 6 F 5 OH ...
The synthesis of fluorotelomer alcohols requires a varying number of tetrafluoroethylene monomers that form an oligomer with a pentafluoroethyl iodide telogen. The fluorinated iodide then undergoes an addition with ethylene to form an organoiodine compound with increased synthesis possibilities. [ 1 ]
Pentafluorophenol is the organofluorine compound (specifically a fluoroalcohol) with the formula C 6 F 5 OH. This is the perfluorinated analogue of phenol. It is a white solid that melts just above room temperature, and smells of phenol. With a pK a of 5.5, it is one of the most acidic phenols.
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 ...
2-Fluoroethanol was originally synthesized by treating 2-chloroethanol with potassium fluoride, in a simple Finkelstein reaction. [5] The product has a lower boiling point that the starting material and may be conveniently isolated by distillation.
This page is the template for the metabolic pathways template. This template should be used to illustrate the general 'shape' of metabolism within the cell . This template is part of the Metabolic Pathways task force .
It is also relatively acidic, with a pKa of 9.3, comparable to that for phenol. [1] It is classified as a hard Lewis acid and its acceptor properties are discussed in the ECW model. [3] [4] Hexafluoro-propan-2-ol is a speciality solvent for organic synthesis, particularly for
al(o(ch 2 ch 2) n ch 2 ch 3) 3 +3h 2 o → al(oh) 3 + ch 3 ch 2 (ch 2 ch 2) n oh The temperature of the reaction influences the molecular weight of alcohol growth. Temperatures in the range of 60-120°C form higher molecular weight trialkylaluminium while higher temperatures (e.g., 120-150 °C) cause thermal displacement reactions that afford ...