Aromaticity MCQs

Aromatic hydrocarbons, also known as arenes, may or may not include a benzene ring. Historically, they were named for their distinctive aroma, but today, a compound is classified as aromatic if it adheres to Hückel’s Rule of aromaticity. According to this rule, a compound is aromatic if it has a planar ring structure with delocalized π electrons and a number of π electrons equal to (4n+2)π, where n is a non-negative integer (0, 1, 2, etc.). Examples include benzene, naphthalene, anthracene, the cyclopentadienyl anion, and the cycloheptatrienyl cation.

(a) Benzene easily undergoes addition due to unsaturation
(b) π-electrons are delocalised in the benzene ring
(c) Three isomeric forms are formed on monosubstitution of benzene
(d) Two types of C-C bonds are present in benzene

(b) π-electrons are delocalised in the benzene ring

(a) NO2+
(b) NO2
(c) NO3
(d) HNO3

(a) NO2+

(a) 110 pm
(b) 156 pm
(c) 121 pm
(d) 139 pm

(d) 139 pm

(a) Delocalisation of π-electrons
(b) Resonance
(c) Greater stability
(d) Electrophilic additions

(d) Electrophilic additions

(a) →
(b) ≡
(c) ↔
(d) ⇌

(c) ↔

(a) Cyclic
(b) Planar
(c) (4n+2) π electrons
(d) All of the above

(d) All of the above

(a) -NO2 is deactivating and m-directing
(b) -Cl is activating and o, p-directing
(c) -OH is activating and o, p-directing
(d) -CH3 is activating and o, p-directing

(b) -Cl is activating and o, p-directing

(a) 6
(b) 8
(c) 2
(d) 4

(a) 6

(a) Planar C6 ring
(b) Localised π bonding
(c) sp2 hybridised C atoms
(d) It shows reactions characteristics of C=C double bonds

(d) It shows reactions characteristics of C=C double bonds

Aromaticity-1

C