Surfactants that are prepared by reaction of ethylene oxide with the appropriate alkyl phenol. These surfactants are cheap to produce but suffer from biodegradability and potential toxicity.
Phenol is acidic because it contains a hydroxyl group directly attached to an aromatic ring, allowing it to donate a proton. Ethanol, on the other hand, is neutral because the hydroxyl group is not as acidic due to the presence of the alkyl group, which stabilizes the molecule and makes it less likely to donate a proton.
phenol
The suffix for alkyl groups is -yl.
The derivative of Phenol is Carbolic acid.
Yes, at room temperature bromine reacts with phenol and forms 2,4,6-tribromo phenol.
The Williamson ether synthesis of Phenacetin is a substitution reaction to form an ether, so it is neither oxidation nor reduction. It involves the reaction of an alkyl halide with a phenol in the presence of a base to form the ether product.
Depending on the desired definition of the word "contaminant" Alkyl Benzene Sulfonate is more likely the answer. Linear Alkyl Sulfonates are far more readily biodegraded than Alkyl Benzene Sulfonate due to their relative chemical structures. Alkyl Benzene Sulfonate can cause issues in waterways such as eutrophication, which in turn can lead to algal blooms.
an example of Alkyl halides is R-X ( x represents any halogen) C2F4 is Teflon it is an example of Alkyl Halides
Phenol and carbolic acid are actually the same compound. "Carbolic acid" is an older, colloquial term for phenol.
Butyl! Alkane is CnH2n+2 Alkyl group is alkane - hydrogen CnH2n+1
Phenol is slightly soluble in water due to hydrogen bonding between the hydroxyl group of phenol and water molecules. However, when excess phenol is added, it disrupts the hydrogen bonding network of water molecules, making it less soluble. This is because phenol-phenol interactions become stronger than phenol-water interactions, leading to precipitation.
phenol is used as a odor eliminator