Chemistry Chapter 14 Entry Test MCQs

a. In alkylation, large amount of heat is evolved
b. In alkylation, a poisonous gas is evolved
c. Alkylation is very costly
d. In alkylation, polyalkylated product is formed

d. In alkylation, polyalkylated product is formed

a. In alkylation, large amount of heat is evolved
b. In alkylation, a poisonous gas is evolved
c. Alkylation is very costly
d. Benzene is more stable in acylation

d. Benzene is more stable in acylation

a. Aliphatic compounds
b. Aromatic compounds
c. Heterocyclic compounds
d. Cycloalkanes

b. Aromatic compounds

a. It is a resonance hybrid of a number of canonical forms
b. It forms only one monosubstitution product
c. It has three delocalised pi- molecular orbitals
d. The C – C bond distance in benzene is uniformly 1.397 Å

c. It has three delocalised pi- molecular orbitals

a. Benzene
b. Toluene
c. Benzoic acid
d. Phenol

a. Benzene

a. Benzyl chloride
b. Benzoyl chloride
c. o- and p-hlorotoluenes
d. m-chlorotoluene

c. o- and p-hlorotoluenes

a. 2,4-dinitrotoluene
b. o-nitrotoluene
c. 2,4,6-trinitrotoluene
d. p-nitrotoluene

c. 2,4,6-trinitrotoluene

a. Anisole
b. Nitrobenzene
c. Chlorobenzene
d. Phenol

b. Nitrobenzene

a. (i) Sodium hydroxide and (ii) sulphuric acid
b. (i) Direct sunlight and (ii) anhydrous AlCl3
c. (i) Anhydrous FeCl3 and (ii) direct sunlight
d. (i) Ultraviolet light and (ii) anhydrous FeCl3

c. (i) Anhydrous FeCl3 and (ii) direct sunlight

a. Soda lime and zinc dust
b. Zinc dust and soda lime
c. Soda lime and copper
d. Zinc dust and sodium hydroxide

a. Soda lime and zinc dust

a. Addition of three C2H2 molecules
b. Substitution of three acetylene molecules
c. Condensation of three C2H2 molecules
d. Polymerisation of three C2H2 molecules

d. Polymerisation of three C2H2 molecules

a. Alkylation-Nitration-Halogenation
b. Alkylation-halogenation-nitration
c. All process occurs at same time
d. Nitration-alkylation-halogenation

d. Nitration-alkylation-halogenation

a. (C6H5)2CH—
b. C6H5CH2
c. C6H5C—
d. C6H5CH—

c. C6H5C—

a. cyclopropenyl cation
b. Cycloheptatriene
c. Naphthalene=C10H8
d. cyclopentadienyl anion

b. Cycloheptatriene

a. Fluorination < chlorination < bromination
b. Fluorination > chlorination > bromination
c. Fluorination > chlorination < bromination
d. Fluorination < chlorination > bromination

b. Fluorination > chlorination > bromination

a. three types
b. one type
c. six types
d. two types

b. one type

a. There is cyclic delocalisation of pi-electrons in benzene
b. Because of unsaturation benzene easily undergoes addition
c. Monosubstitution of benzene gives three isomeric products.
d. There are two types of C – C bonds in benzene molecule

a. There is cyclic delocalisation of pi-electrons in benzene

a. 4sp3 hybrid carbons
b. 2sp2 hybrid carbons
c. 3sp3 hybrid carbons
d. 3sp2 hybrid carbons

b. 2sp2 hybrid carbons

a. 15
b. 6
c. 18
d. 12

c. 18

a. they have a relatively high percentage of hydrogen
b. they have a ring structure of carbon atoms
c. they have a relatively high percentage of carbon
d. they resist reaction with oxygen of air

c. they have a relatively high percentage of carbon

a. Chlorobenzene
b. Acetylene
c. Phenol
d. All the above

d. All the above

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

c. Electrophilic additions

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

a. -Cl is activating and o, p-directing

a. 2
b. 3
c. 7
d. 5

a. 2

a. Activating
b. Deactivating
c. Neutral
d. All of the above

a. Activating

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