Yes, at room temperature bromine reacts with phenol and forms 2,4,6-tribromo phenol.
Phenol is not dissolved in a sodium hydroxide solution; having the characteristics of a weak acid phenol react with NaOH.
NO!! Oxygen-Carbon Bond in phenol has double bond character in it due to resonance, which is hard to break.
There need to be more details provided to answer this question. If you are referring to the white precipitate that is produced in the bromination of phenol which is also known as phenylamine by adding bromine(aq) to phenol or phenylamine then the answer is 2,4,6-tribromophenol or it can be written as 2,4,6-tribromophenylamine.
React aniline with HCl/NaNO2 (diazotisation) followed by reaction with KOH to give phenol. Nitration of phenol with fuming nitric acid gives picric acid (or trinitrophenol).
Two magnesium atoms.
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.
tribromophenol is formed.
Phenol + 3Br2 = 2,4,6-tribromophenol + 3HBr Everything you need to know :) http://www.chemguide.co.uk/organicprops/phenol/ring.html
No they don't react together. but phenol is soluble in CHCl3.
Yes
it cant decolourise
The hydroxyl group in phenol is an activating ortho/para director, but has some slight steric hindrance too ortho position substitution. Therefore, the predominant product of reaction between phenol and bromine will be 4-bromophenol, if reaction conditions are carefully controlled. With excess bromine, di- and tri-bromo phenols will be formed.
When aluminum and bromine react, three bromine atoms combine with each aluminum atom.
2,4,6-tribromophenol or TBP for short
Bromine does not react with air because it is not possible. It is a non reactant element.
Yes, silver does react with bromine. Silver becomes oxidized in the presents of bromine gas, that's why silver jewelry tarnishes.
With bromine, it gives the dibromide.