using a data table, calculator, eraser(if needed), pencil or pen
The molar heat of combustion of phenol can be calculated by measuring the heat released when a known amount of phenol is completely burned in a calorimeter. The heat released is then used to calculate the molar heat of combustion using the mass of phenol burned and the molar quantity of phenol. This calculation can be done using the formula: heat released = molar heat of combustion x moles of phenol.
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.
The nitration of phenol is more rapid than that of toluene.
Phenol + 3Br2 = 2,4,6-tribromophenol + 3HBr Everything you need to know :) http://www.chemguide.co.uk/organicprops/phenol/ring.html
There is no reaction between phenol and sodium carbonate
There is no reaction when their molar ratio is around 1...but when phenol is present in excess it gives triphenylphosphate....
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.
Yes, phenol can react with hydrochloric acid to form chlorobenzene. The reaction involves the substitution of a hydrogen atom in the phenol molecule with a chlorine atom from the hydrochloric acid.
phenol
Phenol is flammable.
What are some examples of Phenol
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.
Both water and phenol are very weak acids. Though phenol is the stronger of the two.
1 unit= 1mg phenol liberated in 30 min at 100 degrees f (37.5c) and 9ph
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.
Any phenol that has substituents in a 1, 3 configuration.