323287 \({\text{Phenol}}\xrightarrow{{\text{x}}}\) forms a tribromo derivative. " \(\mathrm{X}\) " is

323288 Read the Statement - A and Statement - B carefully to mark the correct options given below
Statement A :
Picric acid is 2,4,6-trinitrotoluene.
Statement B :
Phenol-2,4-disulphonic acid is treated with conc. \({\mathrm{\mathrm{HNO}_{3}}}\) to get picric acid.

323289 Identify the product (A) obtained in the following reaction
\({\text{Phenol + Concentrated}}\,\,{\text{Nitric}}\,{\text{acid}}\xrightarrow[{{{\text{H}}_{\text{2}}}{\text{S}}{{\text{O}}_{\text{4}}}}]{{{\text{Concentrated}}}}{\text{A}}\)

323290 Statement A :
In case of phenol bromination takes place even in absence of lewis acid whereas bromination of benzene takes place in presence of Lewis acid like \(\mathrm{FeBr}_{3}\).
Statement B :
- OH group attached to benzene ring is highly deactivating.

323287 \({\text{Phenol}}\xrightarrow{{\text{x}}}\) forms a tribromo derivative. " \(\mathrm{X}\) " is

323288 Read the Statement - A and Statement - B carefully to mark the correct options given below
Statement A :
Picric acid is 2,4,6-trinitrotoluene.
Statement B :
Phenol-2,4-disulphonic acid is treated with conc. \({\mathrm{\mathrm{HNO}_{3}}}\) to get picric acid.

323289 Identify the product (A) obtained in the following reaction
\({\text{Phenol + Concentrated}}\,\,{\text{Nitric}}\,{\text{acid}}\xrightarrow[{{{\text{H}}_{\text{2}}}{\text{S}}{{\text{O}}_{\text{4}}}}]{{{\text{Concentrated}}}}{\text{A}}\)

323290 Statement A :
In case of phenol bromination takes place even in absence of lewis acid whereas bromination of benzene takes place in presence of Lewis acid like \(\mathrm{FeBr}_{3}\).
Statement B :
- OH group attached to benzene ring is highly deactivating.

323287 \({\text{Phenol}}\xrightarrow{{\text{x}}}\) forms a tribromo derivative. " \(\mathrm{X}\) " is

323288 Read the Statement - A and Statement - B carefully to mark the correct options given below
Statement A :
Picric acid is 2,4,6-trinitrotoluene.
Statement B :
Phenol-2,4-disulphonic acid is treated with conc. \({\mathrm{\mathrm{HNO}_{3}}}\) to get picric acid.

323289 Identify the product (A) obtained in the following reaction
\({\text{Phenol + Concentrated}}\,\,{\text{Nitric}}\,{\text{acid}}\xrightarrow[{{{\text{H}}_{\text{2}}}{\text{S}}{{\text{O}}_{\text{4}}}}]{{{\text{Concentrated}}}}{\text{A}}\)

323290 Statement A :
In case of phenol bromination takes place even in absence of lewis acid whereas bromination of benzene takes place in presence of Lewis acid like \(\mathrm{FeBr}_{3}\).
Statement B :
- OH group attached to benzene ring is highly deactivating.

323287 \({\text{Phenol}}\xrightarrow{{\text{x}}}\) forms a tribromo derivative. " \(\mathrm{X}\) " is

323288 Read the Statement - A and Statement - B carefully to mark the correct options given below
Statement A :
Picric acid is 2,4,6-trinitrotoluene.
Statement B :
Phenol-2,4-disulphonic acid is treated with conc. \({\mathrm{\mathrm{HNO}_{3}}}\) to get picric acid.

323289 Identify the product (A) obtained in the following reaction
\({\text{Phenol + Concentrated}}\,\,{\text{Nitric}}\,{\text{acid}}\xrightarrow[{{{\text{H}}_{\text{2}}}{\text{S}}{{\text{O}}_{\text{4}}}}]{{{\text{Concentrated}}}}{\text{A}}\)

323290 Statement A :
In case of phenol bromination takes place even in absence of lewis acid whereas bromination of benzene takes place in presence of Lewis acid like \(\mathrm{FeBr}_{3}\).
Statement B :
- OH group attached to benzene ring is highly deactivating.