Free Phenols MCQs with Answers

63 Phenols MCQs from Chemistry, each with the correct answer and a written explanation of why it is correct. Free and unlimited, with no account needed.

Phenols contain a hydroxyl group directly bonded to an aromatic ring, making them more acidic than alcohols because the phenoxide ion is resonance-stabilised. Reactions include ionisation with bases, electrophilic substitution, bromination, nitration and oxidation, with attention to the difference between phenols and aliphatic alcohols.

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63 questions · page 2 of 4

  • A. Reaction with sodium metal only
  • B. Oxidation of phenol only
  • C. Both A and B
  • D. Neither A nor B

Explanation: The explanation for this question will be added soon!

Correct answer: Both A and B
  • A. Resorcinol
  • B. Aspirin
  • C. Picric acid
  • D. Mesitol

Explanation: The structure shown above is of Picric acid.

Correct answer: Picric acid
  • A. Option A
  • B. Option B.
  • C. Option C
  • D. Option D
  • E. Option E

Explanation: This structure is just a factual recall:

Correct answer: Option E
  • A. It is colourless crystalline molecular solid
  • B. It is poisonous in nature
  • C. It is used as a disinfectant in hospitals and washrooms
  • D. It is sparingly soluble in water

Explanation: Phenol typically appears as a white crystalline solid, but it can also be colorless in its pure form.

Correct answer: It is colourless crystalline molecular solid
  • A. p-Cresol
  • B. Catechol
  • C. Resorcinol
  • D. Quinol

Explanation: The explanation for this question will be added soon!

Correct answer: p-Cresol
  • A. Option A
  • B. Option B
  • C. Option C
  • D. Option D

Explanation: The explanation for this question will be added soon!

Correct answer: Option B
  • A. Mesitylene
  • B. Resorcinol
  • C. Durene
  • D. Anthracene

Explanation: The common name of 1,3-dihydroxybenzene is Resorcinol. The other options are different aromatic compounds:Mesitylene…

Correct answer: Resorcinol
  • A. Cumene
  • B. Toluene
  • C. Benzene
  • D. Aniline

Explanation: The compound that forms phenol when oxidized by atmospheric oxygen in the presence of a metal catalyst is cumene (isopropylbenzene).

Correct answer: Cumene
  • A. Williamson synthesis
  • B. Cannizzaro reaction
  • C. Aldol reaction
  • D. Kolbe-Schmitt reactio

Explanation: The reaction of the sodium salt of phenol with CO₂ is called the Kolbe-Schmitt reaction.

Correct answer: Kolbe-Schmitt reactio
  • A. Picric acid
  • B. Resorcinol
  • C. Catechol
  • D. P-Cresol
  • E. Hydroquinone

Explanation: The explanation for this question will be added soon.

Correct answer: P-Cresol
  • A. Oxidation
  • B. Reduction
  • C. Dehydroxylation
  • D. Dehydrogenation

Explanation: Benzene can be prepared from phenols too through their reduction. In this process, vapors of phenol are passed over heated zinc dust.

Correct answer: Reduction
  • A. Lucas test
  • B. Halogenation
  • C. Nitration
  • D. Iodoform

Explanation: Phenols react with bromine water to give a white ppt. of 2,4,6-tribromophenol. Alcohols do not have any action with bromine water.

Correct answer: Halogenation
  • A. Reduction with hydrogen in the presence of Ni
  • B. Reduction with zinc
  • C. Reduction with alkali
  • D. Reduction wilh acids

Explanation: Phenols, on heating with Zn dust yield aromatic hydrocarbons.

Correct answer: Reduction with zinc
  • A. Colorless crystalline solid
  • B. White crystalline deliquescent solid
  • C. Colorless amorphous solid
  • D. Colorless amorphous deliquescent solid

Explanation: Pure phenol is a white crystalline solid, smelling of disinfectant.

Correct answer: White crystalline deliquescent solid
  • A. Lucas test
  • B. Halogenations
  • C. Nitration
  • D. Idoform test

Explanation: phenol forms white precipitates when reacted with Bromine while alcohol does notP

Correct answer: Halogenations
  • A. Carpolic acid
  • B. Carbonylic acid
  • C. Carbolic acid
  • D. Carbolylic acid

Explanation: The other name for phenol is Carbolic acid.

Correct answer: Carbolic acid
  • A. Delocalization of negative charge in OH group
  • B. Delocation of positive charge on the carbon atom in ring
  • C. Delocalization of negative charge in the ring
  • D. Delocalization of positive charge in the OH group

Explanation: Phenol is more acidic than alcohols due to stabilisation of phenoxide ion through resonance of negative charge in the ring.

Correct answer: Delocalization of negative charge in the ring
  • A. Salicylic acid
  • B. Picric acid
  • C. Cresol
  • D. O-nitrophenol

Explanation: Option A: Salicylic acid is a phenol derivative with a hydroxyl group (-OH) attached to an aromatic ring.

Correct answer: Picric acid
  • A. Ortho-hydroxy benzene sulphonic acid
  • B. Para-hydroxy benzene sulphonic acid
  • C. Meta-hydroxybenzene sulphonic acid
  • D. Both a and b

Explanation: The reaction of phenol with concentrated sulphuric acid is thermodynamically controlled.

Correct answer: Para-hydroxy benzene sulphonic acid
  • A. OH group
  • B. Phenoxide ion
  • C. Benzene ring
  • D. All of these options are correct

Explanation: OPTION A: Phenol is an aromatic alcohol, and the presence of a hydroxyl (OH) group in the molecule makes it an electrophilic substrate.

Correct answer: OH group