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Which molecule would be considered a derivative of phenol?
Cresol is a derivative of phenol. It is an organic compound with a similar structure to phenol, but with a methyl group attached to the benzene ring.
In Reimer Tiemann reaction of phenol with CCl4 to from the trichloromethane derivative what is the electrophile or the mechanism?
In the Reimer-Tiemann reaction, the electrophile is the carbene (CHCl3) that forms from the reaction of phenol with CCl4 in the presence of a base such as NaOH. This carbene then reacts with phenol to form the trichloromethane derivative. The mechanism involves the generation of the carbene intermediate, which attacks the phenol molecule to form the final product.
What is the structure of p bromophenol?
Now this is a benzene ring with a Hydroxide on top, and a bromide on bottom; the p means opposite side
Does phenol react with bromine?
Yes, at room temperature bromine reacts with phenol and forms 2,4,6-tribromo phenol.
What is a substituted phenol?
Any phenol that has substituents in a 1, 3 configuration.
Which molecule would be considered a derivative of phenol?
Cresol is a derivative of phenol. It is an organic compound with a similar structure to phenol, but with a methyl group attached to the benzene ring.
In Reimer Tiemann reaction of phenol with CCl4 to from the trichloromethane derivative what is the electrophile or the mechanism?
In the Reimer-Tiemann reaction, the electrophile is the carbene (CHCl3) that forms from the reaction of phenol with CCl4 in the presence of a base such as NaOH. This carbene then reacts with phenol to form the trichloromethane derivative. The mechanism involves the generation of the carbene intermediate, which attacks the phenol molecule to form the final product.
What is an aryloxyphenoxypropionate?
An aryloxyphenoxypropionate is another name for aryloxy-phenoxy-propionate, a univalent radical of a derivative of phenol, and the salt or ester from it, used as a food preservative.
What is the structure of p bromophenol?
Now this is a benzene ring with a Hydroxide on top, and a bromide on bottom; the p means opposite side
Structure of phenol?
phenol
Does phenol react with bromine?
Yes, at room temperature bromine reacts with phenol and forms 2,4,6-tribromo phenol.
Can you get phenol from carbolic acid?
Phenol and carbolic acid are actually the same compound. "Carbolic acid" is an older, colloquial term for phenol.
Is it derivative of or derivative from?
"Derivative of"
What is phenol used for in medical practices?
phenol is used as a odor eliminator
What is a substituted phenol?
Any phenol that has substituents in a 1, 3 configuration.
Why phenol does not dissolve in water when excess?
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.
What increase absorbance of phenol in ethanol?
Possible factors that can increase the absorbance of phenol in ethanol are: increasing the concentration of phenol in the solution, using a higher path length cuvette for measurement, and selecting a wavelength for measurement where phenol has a higher molar absorptivity coefficient.
