Concept:
Phenol contains an \( -OH \) group attached to the benzene ring.
The \( -OH \) group is:
- Electron donating
- Strongly activating
- Ortho and para directing
Thus, electrophilic substitution occurs readily at the ortho and para positions.
Step 1: {Reaction with bromine water.}
When phenol reacts with bromine water:
\[
C_6H_5OH + 3Br_2 \rightarrow C_6H_2Br_3OH + 3HBr
\]
Step 2: {Substitution positions.}
Because phenol strongly activates the ring, bromination occurs at:
\[
2\text{-position},\;4\text{-position},\;6\text{-position}
\]
Step 3: {Major product.}
The product formed is:
\[
2,4,6-tribromophenol
\]
This compound forms as a
white precipitate in bromine water.