Which of the following compounds will give a ketone on oxidation with chromic anhydride (CrO₃) ?
(A) (CH₃)₂CH – CH₂OH
(B) CH₃CH₂CH₂OH
(C) (CH₃)₃C – OH
(D) CH₃ – CH₂ – CH(OH) – CH₃
Class 12 · Chemistry · CBSE Board · 2016–2025
Alcohols, Phenols and Ethers — Class 12 Chemistry PYQs
79 questions from this chapter, asked in 8 Class 12 exams between 2016–2025 — every question paper set included, duplicates removed.
Questions asked per year
Practice questions first 10 of 79 — free
Which of the following is most acidic ?
(A) Benzyl alcohol
(B) Phenol
(C) Cyclohexanol
(D) p-Chlorophenol
Phenol is less acidic than :
(A) ethanol
(B) o-nitrophenol
(C) o-methoxyphenol
(D) o-methylphenol
(CH₃)₃ C – O – CH₃ reacts with HI to give :
(A) (CH₃)₃ C – I + CH₃OH
(B) (CH₃)₃ C – I + CH₃ – I
(C) (CH₃)₃ C – OH + CH₃ – I
(D) (CH₃)₃ C – OH + CH₃OH
(CH₃)₂ CH – O – CH₃ reacts with HI to give :
(A) (CH₃)₂CH – OH + CH₃ – OH
(B) (CH₃)₂CH – OH + CH₃ – I
(C) (CH₃)₂CH – I + CH₃ – OH
(D) (CH₃)₂CH – I + CH₃ – I
Anisole reacts with HI to give :
(A) Phenol + CH₃ – I
(B) Iodobenzene + CH₃ – OH
(C) Benzyl alcohol + CH₃ – I
(D) Benzyl iodide + CH₃ – OH
A compound (X) with the molecular formula C₃H₈O can be oxidized by strong oxidizing agents to another compound (Y) whose molecular formula is C₃H₆O₂. The compound (X) is :
(A) CH₃ – CH₂ – O – CH₃
(B) CH₃ – CH(OH) – CH₃
(C) CH₃ – CH₂ – CH₂ – OH
(D) None of the above
Ethanol on heating with conc. H₂SO₄ at 413 K gives :
(A) C₂H₅OSO₃H
(B) C₂H₅ – O – CH₃
(C) C₂H₅ – O – C₂H₅
(D) CH₂ = CH₂
Aspirin is formed by the acetylation of :
(A) Benzoic acid
(B) Phenol
(C) Salicylic acid
(D) Phthalic acid
Dehydration of tertiary alcohols with Cu at 573 K gives :
(A) Alkyne
(B) Alkene
(C) Aldehyde
(D) Ketone
Why practise Alcohols, Phenols and Ethers PYQs?
Alcohols, Phenols and Ethers has appeared in 8 Class 12 Chemistry exams we track between 2016–2025, with questions worth 1, 2, 3, 5 marks. CBSE Board examiners consistently reuse concepts and question patterns from this topic — practising its previous year questions is the most reliable way to know exactly what to expect in your exam.