Answer:
conc. fuming, 1 mol H2SO4
Dilute NaOH
Br2
Dilute H2SO4
Step-by-step explanation:
The synthesis of ortho-bromophenol follows the reaction sequence shown in the image attached.
First of all, the phenol is sulphonated using concentrated sulphuric acid at 100°C. Carrying out the reaction at 100°C ensures that the para-isomer predominates. Lower temperatures favour the formation of the ortho isomer. Dilute sodium hydroxide is added before the addition of bromine.
Bromine molecule is then added. The incoming electrophile now attaches to the ortho position. Dilute acid is added at 100°C to remove the -SO3H thereby obtaining the Ortho-bromophenol