using a data table, calculator, eraser(if needed), pencil or pen
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 at 25 C degrees is a solid.
C6H5OH BOILING POINT- 1820C C6H5CH3 BOILING POINT- 1110C === ===
what is the chemical equation when phenol react with hydrochloric acid
phenol
The total solid content of the resin can be determined by weighing 2 grams of it in an aluminum dish. It must be placed in an oven set to 100 degrees Celsius for 2 hours, and then the dry resin can be used to calculate the solid content.
Phenol is flammable.
phenol
This is because the two isomers have different boiling points and one of which falls under 100 degrees celsius (2-nitrophenol). hence the first to evaporate out is the 2nitrophenol and the rest will be 4nitrophenol. This is because the two isomers have different boiling points and one of which falls under 100 degrees celsius (2-nitrophenol). hence the first to evaporate out is the 2nitrophenol and the rest will be 4nitrophenol.
What are some examples of Phenol
Yes, at room temperature bromine reacts with phenol and forms 2,4,6-tribromo phenol.
Both water and phenol are very weak acids. Though phenol is the stronger of the two.
Phenol. Phenol's Dipole Moment: 1.7D Phenyl chloride's Dipole Moment: 1.54D