WorksheetsBenzene
Total questions: 21
Worksheet time: 11mins
State the type of mechanism for the reaction:
Nucleophilic Addition
Electrophilic Addition
Nucleophilic Substitution
Electrophilic Aromatic Substitution
Choose the method for the preparation of benzoic acid from ethyl benzene.
Heated with concentrated HNO3
Heated with alkaline KMnO4 followed by acidification
Addition of Cl2 in the presence of sunlight followed by the addition of NaOH in CH3CH2OH
Addition of Cl2 in the presence of sunlight followed by boiling with aqueous NaOH
Indicate the correct names for the following amines. Notice that for some of them, two names are applicable: an IUPAC name and a common name
1-methyl-3-bromoaniline
N-methyl-3-bromoaniline
1-aminomethyl-3-bromobenzene
3-bromo-N-methylaniline
Which reagent would be used for the nitration of benzene?
I. mixture of concentrated nitric and sulphuric acids
HNO3/H2SO4
II. sodium nitrate(V) NaNO3
III. sodium nitrate(III) NaNO2
I only
I and II only
II and III only
I, II and III
Which of the following compound is aromatic haloalkane?
I. C6H5Cl
II. C6H5CH2Cl
III. CH3CH2Cl
I only
I and II only
II and III only
I, II and III
The following reaction is known as
Friedel-Crafts acylation
Hoffman’s Degradation
Coupling reaction
Friedel-Crafts alkylation
The product formed when an ethylbenzene is refluxed with acidic potassium (VII) manganate is
C6H5CHO
C6H5COOH
C6H5CH2OH
C6H5CH2COOH
What are the best structures for U and V in the following reaction:
Choose the correct statement
Carbon to carbon bond in benzene have the same bond length
Cyclobutene has delocalised electrons
C=C bond in cyclobutene is longer than C-C bond in butane
All atoms in cyclobutene, pentane and benzene are planar
Which compound below is aromatic?
Which of the following statement is true of the mechanism of nitration of benzene?
NO2+, nitronium ion is the nucleophilic
The reaction involved free radicals
Sulfuric acid acts as an electrophile
NO2+, nitronium ion is formed the reaction of concentrated sulfuric acid and concentrated nitric acid
Benzene reacts with chloromethane in AlCl3 to form methylbenzene. The function of AlCl3 is
produce a nucleophile
reduce the activation energy
produce an electrophile
reduce the temperature
W is an aromatic organic acid which reacts with 2 moles of NaOH for neutralization. W is formed from X which has a molecular formula; C8H10. Pick the correct statement.
X is ethylbenzene
X contains deactivating groups
W contains 2 carboxyl groups and X contains 2 methyl groups
X undergoes electrophilic addition
Which of the following can be used to differentiate benzene from toluene?
Brady's test
Tollen's reagent
Oxidation test
Hinsberg's test
What is the IUPAC name of the following compound?
1-bromo-3-fluoronitrobenzene
4-bromo-2-fluoronitrobenzene
5-bromo-1-fluoronitrobenzene
3-bromo-1-fluoronitrobenzene
What is the IUPAC name of the following compound?
4-bromo-3-chlorotoluene
4-bromo-5-chlorotoluene
1-bromo-2-chlorotoluene
2-bromo-1-chlorotoluene
Which of the following statements about benzene is true?
All the six hydrogens are on the same plane.
The actual benzene structure is the rapid equilibrium of the two Kekule's structure.
All carbon atoms are sp-hybridised.
Benzene is a gas at room temperature.
What is the description of benzene ring in the following reaction?
A Lewis base
A Lewis Acid
A Bronsted-Lowry base
A Bronsted-Lowry acid
What is the characteristic observation when phenol reacts with iron (III) Chloride?
Brick-red precipitation
blue-voilet colouration
white precipitation
homogenous solution
Which of the following statements about benzene are true?
I. Benzene does not undergo addition reaction
II. there are six pi electrons in the benzene ring
III. All the C-C bonds length in benzene are equivalent
I only
I and II only
II and III only
I, II and III
Which of the following statements are true regarding the electrophilic aromatic substitution reaction?
I. It is exclusive for benzene derivative only
II. It involves the formation of positively charge reactive intermediate.
III. The aromaticity is retained after the reaction.
I only
I and II only
II and III only
I, II and III
