using a data table, calculator, eraser(if needed), pencil or pen
Phenol + 3Br2 = 2,4,6-tribromophenol + 3HBr Everything you need to know :) http://www.chemguide.co.uk/organicprops/phenol/ring.html
The substitution reactions of phenol are easier than benzene, phenol directly reacts with bromine and gives tribromo phenol while benzene requires FeCl3 as a catalyst and gives mono bromo phenol.
There are three elements. They are carbon,hydrogen and oxygen.
There is no reaction when their molar ratio is around 1...but when phenol is present in excess it gives triphenylphosphate....
The reaction product of bromine and phenol is 2,4,6-tribromophenol. In this reaction, the bromine replaces the hydrogen atoms on the phenol ring to form a tribrominated product.
Phenol is a solid at 25 degrees Celsius.
Though butanol may refer to any of 4 different compounds (depending on the placement of the alcohol group), all are liquids are room temperature.
Phenol is a solid at room temperature (25°C). It has a melting point of 40.5°C, so at 25°C, it would exist in a solid state.
what is the chemical equation when phenol react with hydrochloric acid
phenol
The derivative of Phenol is Carbolic acid.
The boiling point of alcohol can vary depending on the type of alcohol. For example, the boiling point of ethanol (found in alcoholic beverages) is around 78.37°C (173.07°F). Isopropyl alcohol, often used as rubbing alcohol, has a boiling point of around 82.6°C (180.7°F).
Yes, at room temperature bromine reacts with phenol and forms 2,4,6-tribromo phenol.
Phenol and carbolic acid are actually the same compound. "Carbolic acid" is an older, colloquial term for phenol.
1 unit= 1mg phenol liberated in 30 min at 100 degrees f (37.5c) and 9ph
phenol is used as a odor eliminator
Any phenol that has substituents in a 1, 3 configuration.