Halogenation of Benzene
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- C6H6+Cl2FeCl3−−−→
- C6H6+HOClH+−−→
- C6H6+I−ClZnCl2−−−−→
- C6H6+Cl2AlCl3−−−→
- Monochlorobenzene
- Trichlorobenzene
- Hexachlorobenzene
- Benzene hexachloride
- C6H5Cl
- o−C6H4Cl2
- C6H6Cl6
- p−C6H4Cl2
- Nitrobenzene
- Phenol
- Anisole
- Chlorobenzene
In the following question two Statement-I (Assertion) and Statement-2 (Reason) are provided. each question has 4 choices (a), (b), (c) and (d) for its answer, out of which Only One is correct. Mark your responses from the following options:
Statement-1: Aniline becomes more reactive towards electrophilic aromatic substitution in presence of strongly acidic solution.
Statement-2: The amino group is completely protonated in strongly acidic medium. Thus the lone pair of electrons on the nitrogen is no longer available for resonance.
Both Statement-1 and Statement-2 are true and Statement-2 is the correct explanation of Statement-1.
Both Statement-1 and Statement-2 are true and Statement-2 is not the correct explanation of Statement-1.
Statement-1 is true but Statement-2 is false.
Statement-1 is false but Statement-2 is true.
- C6H5Cl
- o−C6H4Cl2
- C6H6Cl6
- p−C6H4Cl2
What is the chief product obtained when n-butane is treated with bromine in the presence of light at 130∘C
C6H5CH3I, C6H5COOHII, C6H6III, C6H5NO2IV
- I>II>III>IV
- I>III>II>IV
- II>III>IV>I
- III>I>II>IV
C6H5CH3I, C6H5COOHII, C6H6III, C6H5NO2IV
- I>II>III>IV
- I>III>II>IV
- II>III>IV>I
- III>I>II>IV