General Mechanism of Electrophilic Aromatic Substitution
Trending Questions
Q. The electrophilic aromatic substitution proceeds through :
Q. (I) Chlorobenzene (II) 2, 4−dinitrochlorobenzene (III) p−nitrochlorobenzene
The decreasing order of their reactivities towards electrophilic substitution reaction is:
The decreasing order of their reactivities towards electrophilic substitution reaction is:
- (I)>(II)>(III)
- (I)>(III)>(II)
- (II)>(I)>(III)
- (III)>(I)>(II)
Q. Identify the position where electrophilic aromatic substitution (EAS) is most favourable.
- A
- B
- C
- A and C
Q. Statement-1: Benzene and ethene both react with electrophilic reagents.
Statements-2: Benzene and ethene both have loosely bound π-electrons, which can be donated to the vacant orbital of the electrophile
Statements-2: Benzene and ethene both have loosely bound π-electrons, which can be donated to the vacant orbital of the electrophile
- Statement-1 is true, Statement-2 is true; Statement-2 is a correct explanation for statement-1
- Statement-1 is true, Statement-2 is true; Statement-2 is NOT a correct explanation for statement-1
- Statement-1 is true, Statement-2 is false
- Statement-1 is false, Statement-2 is true
Q. Among the following compounds, the decreasing order of reactivity towards electrophilic substitution is:
- III>I>II>IV
- IV>I>II>III
- I>II>III>IV
- II>I>III>IV
Q. Which pair of products would result from the acid cleavage of phenyl propyl ether with HBr at an elevated temperature?
- Phenol and 1-bromopropane
- Phenol and 1-propanol
- Bromobenzene and 1-propanol
- Bromobenzene and 1-bromopropane
Q. BenzeneH3C−(CH3)CH−CH2−Cl−−−−−−−−−−−−−−−−→AlCl3
The product formed would be:
The product formed would be:
- All of these
Q. Which of the following electrophilic substitution reactions represent(s) the correct product(s)?
Q. BenzeneH3C−(CH3)CH−CH2−Cl−−−−−−−−−−−−−−−−→AlCl3
The product formed would be:
The product formed would be:
- All of these
Q. Which one of the following is a free-radical substitution reaction
- a
- b
- c
- d