Which one of the following compounds will be most readily attacked by an electrophile?a)Chlorobenzeneb)Phenolc)Benzened)TolueneCorrect answer is option 'B'. Can you explain this answer?

EduRev

All Courses

Explore Courses UPSC Exam UPSC Test Series Free Notes EduRev Infinity

Open App

JEE Exam > JEE Questions > Which one of the following compounds will be ...

Join the Discussion on the App

Which one of the following compounds will be most readily attacked by an electrophile?

a)
Chlorobenzene
b)
Phenol
c)
Benzene
d)
Toluene

Correct answer is option 'B'. Can you explain this answer?

FREE This question is part of

JEE Main Practice Test- 20

Attempt Test

Attempt this Test

View all answers Start learning for free

< Previous Question Next Question >

Explore Courses for JEE exam

Similar JEE Doubts

Which of the following compounds will be most easily attacked by an electrophile ?

View answer

Can you explain the answer of this question below:On the basis of aromaticity, there are three types of compounds i.e. aromatic, non-aromatic and antiaromatic.The increasing order of stability of these compounds are is under:Anti-aromatic compound non-aromatic compound aromatic compounds. Compounds to be aromaticfollow the following conditions (according to valence bond theory)(i) The compounds must be be cyclic in structure having (4n + 2) e, where n = Hckels number = 0, 1,2, 3 et.c(ii) The each atoms of the cyclic structure must have unhybridised p-orbital i.e. the atoms of thecompounds have unhybridised p-orbital i.e. usually have sp2 hybrid or planar.(iii) There must be a ring current of electrons in the ring or cyclic structure i.e. cyclic structure mustundergo resonance .Compounds to be anti-aromatic, it must have 4ne where n = 1, 2 and it must be planar and undergoresonance. Non-aromatic compounds the name itself spells that compounds must be non-planarirrespective of number of electrons. Either it has 4ne or (4n + 2) electrons it does not matter.The rate of reaction of any aromatic compounds depends upon the following factors:(i) Electron density(ii) stability of carbocation producedHigher the amount of electron density of the ring, higher will be its rate towards aromatic electrophilicsubstitution and vice-versa. Similarly, higher will be the stability of the produced carbocation after theattack of electrophile, higher will be its rate towards aromatic electrophilic substitution. There is a greateffect of kinetic labelling on the rate of aromatic electrophilic substitution. As we known that higher theatomic weight or, molecualr weight, higher will be the van der Waals force of attraction or, bond energy.Since there will be effect of kienetic labelling if the 2nd step of the reaction will be the slow step, (r.d.s.)otherwise there will be no effect of kinetic labelling.Q. Which of the following is correct order of the rate of reaction of C6H6, C6D6 and C6T6 towardsnitrations?A:C6H6 C6D6 C6T6B:C6H6 = C6D6 = C6T6C:C6H6 C6D6 = C6T6D:C6T6 C6D6 C6H6The answer is b.

View answer

Among the following, the compound that can be most readily sulphonated is

View answer

On the basis of aromaticity, there are three types of compounds i.e. aromatic, non-aromatic and antiaromatic. The increasing order of stability of these compounds are is under: Anti-aromatic compound < non-aromatic compound < aromatic compounds. Compounds to be aromaticfollow the following conditions (according to valence bond theory)(i) The compounds must be be cyclic in structure having (4n + 2)π e–, where n = Hückel’s number = 0, 1, 2, 3 et.c(ii) The each atoms of the cyclic structure must have unhybridised p-orbital i.e. the atoms of the compounds have unhybridised p-orbital i.e. usually have sp2 hybrid or planar.(iii) There must be a ring current of π electrons in the ring or cyclic structure i.e. cyclic structure mustundergo resonance .Compounds to be anti-aromatic, it must have 4nπe– where n = 1, 2… and it must be planar and undergo resonance. Non-aromatic compounds the name itself spells that compounds must be non-planarirrespective of number of π electrons. Either it has 4nπe– or (4n + 2) π electrons it does not matter.The rate of reaction of any aromatic compounds depends upon the following factors:(i) Electron density(ii) stability of carbocation producedHigher the amount of electron density of the ring, higher will be its rate towards aromatic electrophilic substitution and vice-versa. Similarly, higher will be the stability of the produced carbocation after the attack of electrophile, higher will be its rate towards aromatic electrophilic substitution. There is a great effect of kinetic labelling on the rate of aromatic electrophilic substitution. As we known that higher the atomic weight or, molecualr weight, higher will be the van der Waal’s force of attraction or, bond energy. Since there will be effect of kienetic labelling if the 2nd step of the reaction will be the slow step, (r.d.s.) otherwise there will be no effect of kinetic labelling.Q. Which of the following is correct order of the rate of reaction of C6H6, C6D6 and C6T6 towardssulphonation?

View answer

How many of the following compounds are more reactive than benzene towards electrophilic substitution. Correct answer is '3'. Can you explain this answer?

View answer

Top Courses for JEEView all

Physics for JEE Main & Advanced

Mock Tests for JEE Main and Advanced 2025

Chemistry for JEE Main & Advanced

Mathematics (Maths) for JEE Main & Advanced

Chapter-wise Tests for JEE Main & Advanced