Table of Contents
How do I convert benzene into M Bromophenol?
For the conversion of Benzene to m-Bromophenol, we take the Benzene ring in the Presence of Nitration process such as HNO/H2SO4 that will give Nitrobenzene. This will again go in the Reaction with Br2 giving out the m-Bromonitro Benzene.
How do you convert phenol to M Bromophenol?
Answer
- Nitrate to get nitrobenzene.
- Brominate to get m bromo nitrobenzene.
- Reduce with say Sn/HCl to give m bromo aniline.
- Diazotize with sodium nitrite/HCl to give diazonium salt (not isolated)
- make alkaline and warm to displace N2 giving the phenol.
How do you convert benzene to trinitrotoluene?
First, benzene is treated with methyl chloride and through a mechanism called Friedel crafts reaction. This step converts benzene to toluene and eliminates hydrochloric acid as a by-product. Secondly, toluene is treated with through the process called nitration.
How is phenol converted to Bromophenol?
You have to brominate Phenol in carbon disulfide to obtain 4-Bromophenol. At -30° C, 4-bromophenol is yielded by 97\% and at +30° C, the yield is 82\%. You will need a 5 litre flask fitted with a mechanical stirrer, a reflux condensor and a separatory funnel.
How do you convert benzene to picric acid?
The Wolffenstein–Böters reaction is an organic reaction converting benzene to picric acid by a mixture of aqueous nitric acid and mercury(II) nitrate. The reaction, which involves simultaneous nitration and oxidation, was first reported by the German chemists Richard Wolffenstein and Oskar Böters in 1906.
How do you convert bromo benzene to 1 Phenylethanol?
Answer : when bromobenzene reacts with Mg in dry ether it forms Grignard reagent, further treating with ethanal in acidic condition it forms 1-phenyl ethanol.
How do you convert benzene to M nitrochlorobenzene?
We can convert benzene in m-nitro chlorobenzene by nitration of benzene followed by chlorination of the compound formed by nitration. Step-By-Step answer: Nitration of benzene happens when one or more than one hydrogen atom from the benzene ring is replaced by a nitro group.
How do you make M nitrobenzoic acid from benzene?
One possible route (among many): Friedel-Crafts acylation of benzene with acetyl chloride/FeCl3 to form acetophenone. Nitration with HNO3/H2SO4 to form m-nitroacetophenone. Oxidation of the acetyl group to a carboxylic acid with KMnO4 or H2CrO4.
How do you convert phenol to o bromophenol?
How do you get phenol from Benzene?
How is phenol obtained commercially from benzene? Benzene react with chlorine in the presenc of ferric chloride which form chlorobezene, which on further reaction with sodium hydroxide gives sodium phenoxide. Then sodium phenoxide acidified and form phenol.