Br\(_2\)/CS\(_2\)
When phenol reacts with bromine in carbon disulfide (CS\(_2\)), an electrophilic substitution reaction occurs, where the hydroxyl group (OH) activates the ring towards substitution at the ortho and para positions. The major product is 2,4,6-Tribromophenol, as bromine atoms are added at the ortho and para positions relative to the hydroxyl group. \[ \text{C}_6\text{H}_5\text{OH} + 3\text{Br}_2 \xrightarrow{\text{CS}_2} \text{C}_6\text{H}_2\text{Br}_3\text{OH} \]
Given below are two statements:
Statement (I): Alcohols are formed when alkyl chlorides are treated with aqueous potassium hydroxide by elimination reaction.
Statement (II): In alcoholic potassium hydroxide, alkyl chlorides form alkenes by abstracting the hydrogen from the $ \beta $-carbon.
In the light of the above statements, choose the most appropriate answer from the options given below:
In which of the following reactions, major product is matched correctly?
Total number of nucleophiles from the following is: \(\text{NH}_3, PhSH, (H_3C_2S)_2, H_2C = CH_2, OH−, H_3O+, (CH_3)_2CO, NCH_3\)
In the following substitution reaction:
The correct IUPAC name of \([ \text{Pt}(\text{NH}_3)_2\text{Cl}_2 ]^{2+} \) is: