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Class 12 Chemistry — Chapter 7: Alcohols, Phenols and Ethers

96 practice questions · 32 Easy · 32 Medium · 32 Hard

Practise Class 12 Chemistry Chapter 7, "Alcohols, Phenols and Ethers", with 96 NCERT-aligned multiple-choice questions. The set is split into 32 Easy, 32 Medium and 32 Hard questions, so you can warm up on the fundamentals and then push into the exam-level problems that separate top scorers in CBSE Board exams, JEE Main, JEE Advanced and NEET UG.

"Alcohols, Phenols and Ethers" is one of the chapters where reactions, named concepts, and balanced numerical work really pays off. Each MCQ on this chapter is timed and uses exam-grade marking (+2 correct, −1 wrong, 0 skipped), training the same accuracy-under-pressure that real papers demand. Every question carries a short explanation, so a wrong answer becomes a quick lesson rather than a dead end — the fastest way to close gaps before a test.

Use this chapter as targeted revision: attempt the Easy set first to confirm your basics on Alcohols, Phenols and Ethers, then move to Medium and Hard to test application and problem-solving. Your accuracy, streaks and XP save automatically, and the chapter feeds into your overall Class 12 Chemistry mastery score. A few sample questions are shown below; sign in free to practise all 96.

Key concepts: Alcohols, Phenols and Ethers (Class 12 Chemistry)

This chapter covers the preparation, properties and reactions of alcohols, phenols and ethers, and the acidic nature of phenols.

Classification & preparation
Alcohols (–OH on sp³ C), phenols (–OH on aromatic ring) and ethers (R–O–R'); prepared from alkenes, carbonyls, haloalkanes (Williamson synthesis for ethers).
Acidity of phenols
Phenols are more acidic than alcohols because the phenoxide ion is stabilised by resonance; electron-withdrawing groups increase acidity.
Reactions of alcohols
Undergo dehydration to alkenes, oxidation to carbonyls/acids, and esterification with acids.
Electrophilic substitution in phenol
The –OH group is ortho/para directing and activating, so phenol readily undergoes nitration, halogenation and the like.
Important reactions
Kolbe's reaction (salicylic acid), Reimer–Tiemann reaction (salicylaldehyde), and Williamson ether synthesis.

💡 Exam tips for Alcohols, Phenols and Ethers

  • Phenol is more acidic than alcohols (resonance-stabilised phenoxide) but less acidic than carboxylic acids.
  • Use Williamson synthesis (alkoxide + primary haloalkane) for unsymmetrical ethers to avoid elimination.

Sample questions

Q1Easy

Functional group of alcohol:

A.−OH✓ correct
B.−COOH
C.−CHO
D.−NH₂
Why

Hydroxyl group.

Q2Medium

Phenol is more acidic than alcohol because:

A.Phenoxide ion is resonance stabilised✓ correct
B.It's smaller
C.It's volatile
D.No reason
Why

Negative charge delocalised over benzene ring.

Q3Hard

Williamson ether synthesis uses:

A.Alkoxide + alkyl halide (Sn2)✓ correct
B.Alcohol + acid
C.Two alcohols
D.Carbonyl + amine
Why

Best with primary halides to avoid elimination.

Alcohols, Phenols and Ethers — FAQs

What are the key concepts in Class 12 Chemistry Alcohols, Phenols and Ethers?+

This chapter covers the preparation, properties and reactions of alcohols, phenols and ethers, and the acidic nature of phenols. Key ideas include Classification & preparation, Acidity of phenols, Reactions of alcohols, Electrophilic substitution in phenol, Important reactions.

What does Class 12 Chemistry Chapter 7 (Alcohols, Phenols and Ethers) cover on XamBaaz?+

It covers 96 NCERT-aligned MCQs on "Alcohols, Phenols and Ethers" — 32 Easy, 32 Medium and 32 Hard — each with a timed quiz and an instant explanation, suitable for CBSE Board exams, JEE Main, JEE Advanced and NEET UG.

Are these "Alcohols, Phenols and Ethers" questions free to practise?+

Yes — sign in with Google to practise "Alcohols, Phenols and Ethers" free. Full unlimited access is ₹999/year (limited-time launch price), with no per-chapter charges.

How should I revise "Alcohols, Phenols and Ethers" for the exam?+

Start with the Easy quiz to confirm your fundamentals, then attempt Medium and Hard for application-level practice. Review each explanation, retry the questions you miss, and track your accuracy on this chapter until it is consistently high.

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