All Free Chemistry MCQs with Answers
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13,720 questions · page 603 of 686
- A. Benzene reactivity
- B. That benzene has dual character
- C. That benzene has less heat of formation
- D. All of these options are correct
Explanation: Kekule's structure does not explain the extra ordinary stable nature of benzene molecule and its lack of reactivity towards addition…
Correct answer: All of these options are correct- A. Tetrahedral
- B. Hexagonal planar
- C. Hexagonal irregular
- D. Trigonal planar
Explanation: A benzene ring has 6 carbons hence it is a hexagon and it is hexagonal planar and not hexagonal irregular because all the carbons are in…
Correct answer: Hexagonal planar12043. Which one of the following is a strong electrophile on which benzene electrons attack fastly?
- A. FeBr3
- B. FeCl4-
- C. Cl+
- D. Cl-
Explanation: Electrophiles are species with a positive charge. The only element/molecule with a positive charge is Cl hence, Option C is the correct…
Correct answer: Cl+- A. Hexagonal planar
- B. Square planar
- C. Trigonal planar
- D. Linear
Explanation: Benzene has 6 carbons, hence it is given the name hexagon. All the carbons are in the same planar hence it is called planar.
Correct answer: Hexagonal planar- A. KMnO4
- B. K2Cr2O7
- C. KHMnO4
- D. V2O5
Explanation: Vanadium pentoxide (V2O5) can be used as an oxidizing agent to oxidize benzene and its derivatives under specific conditions.
Correct answer: V2O5- A. Two
- B. One
- C. Three
- D. None of these
Explanation: Benzene can form only one type of monosubstituted means that it cannot form different atoms just by replacing the position of the attached…
Correct answer: One- A. Pyrrole
- B. Furan
- C. Thiophene
- D. All
Explanation: In benzene derivatives, all the atoms that make up the ring are carbon atoms.
Correct answer: All- A. Increases electron density
- B. Decrease electron density on benzene
- C. Make benzene less reactive
- D. None of these
Explanation: The electron donating group such as the alkyl group donates electrons to the benzene ring and hence increases the density.
Correct answer: Increases electron density- A. Elimination
- B. Addition
- C. Substitution
- D. Dehydration
Explanation: There is no such evidence of an elimination reaction in Benzene since it completely destroys its stability.Benzene generally also resists…
Correct answer: Elimination- A. Ortho-xylene
- B. Para-xylene
- C. Para-methyl toluene
- D. Meta-methyl toluene
Explanation: Xylene is any of three organic compounds with the formula (CH3)2C6H4. They are derived from the substitution of two hydrogen atoms with…
Correct answer: Para-xylene- A. Alkyl group
- B. Benzyl group
- C. Phenyl group
- D. Ethyl group
Explanation: Reason: A benzene ring has the formula of C6H6. When a hydrogen atom is removed, this becomes C6H5. C6H5 is known as a phenyl group.
Correct answer: Phenyl group- A. Highly saturated
- B. Highly unsaturated
- C. Gives substitution reactions
- D. Gives elimination reactions
Explanation: Option B. Kekule formula with three double bonds demands a high degree of unsaturation from benzene while usually it exhibits a saturated…
Correct answer: Highly unsaturated- A. Between the C-C bonds of benzene
- B. Above and below the carbon bonds
- C. In the form of cloud above and below the benzene ring
- D. None of these
Explanation: Benzene is a cyclic molecule in which all of the ring atoms are sp2-hybridized.
Correct answer: In the form of cloud above and below the benzene ring- A. Between the C-C bonds of benzene
- B. Above and below the carbon bonds
- C. In the form of a cloud above and below the benzene ring
- D. None of these options is correct
Explanation: All of the carbon atoms in the benzene rings are sp2-hybridized: the overlap of the sp2 orbitals around the ring produces a framework of…
Correct answer: In the form of a cloud above and below the benzene ring- A. Increase electron density at the ortho and para positions
- B. Decrease electron density at the ortho and para positions
- C. Make benzene less reactive
- D. Both Options B and C are correct
Explanation: The meta groups deactivate the ring, by the inductive effect, in the presence of an electronegative atom, that withdraws the electrons…
Correct answer: Both Options B and C are correct- A. Anthracene
- B. Naphthalene
- C. Phenol
- D. None of these options is correct
Explanation: All of these compounds contain a benzene ring, hence all are aromatic.
Correct answer: None of these options is correct- A. In alkynes to identify the position of the triple bond
- B. In arenes to identify the position of the first substitution
- C. In arenes to identify the position of the second substitution
- D. In all hydrocarbons to identify the position of the functional group
Explanation: The terms ortho, meta, and para are prefixes used in organic chemistry to indicate the position of non-hydrogen substituents on a…
Correct answer: In arenes to identify the position of the second substitution- A. Three triple bonds
- B. Two double bonds
- C. Three double bonds
- D. No multiband
Explanation: Option C is correct since benzene is a hydrocarbon composed of six carbons connected via a covalent bond, and exists in the form of a…
Correct answer: Three double bonds12059. What are Kekule structures?
- A. The two isomers of benzene
- B. The isomers of arenes
- C. The two-resonance structure of benzene
- D. The two-resonance structure of phenols
Explanation: This option is correct because kekule structure represents the resonating structure of benzene according to which benzene has a ring…
Correct answer: The two-resonance structure of benzene- A. Two double bonds
- B. Delocalized pi-electron charge
- C. Three double bonds
- D. One sigma bond
Explanation: Benzene has a delocalized pi-electron system. Its alternative double bonds cause the ring to become delocalized and constitute the…
Correct answer: Delocalized pi-electron charge