Home › UP Board Class 12 › chemistry › Alcohols Phenols and Ethers › The LUCAS REAGENT is used to distinguish between…
The LUCAS REAGENT is used to distinguish between primary, secondary, and tertiary alcohols. It consists of
Aconcentrated $\mathrm{H_2SO_4}$ + $\mathrm{KMnO_4}$
BPCC + dichloromethane
Cconcentrated HCl + anhydrous $\mathrm{ZnCl_2}$
DNaOH + ethanol
Answer & Solution
Correct answer: C. concentrated HCl + anhydrous $\mathrm{ZnCl_2}$
1. NCERT §7.4 describes the Lucas test.
2. REAGENT: concentrated HCl + anhydrous $\mathrm{ZnCl_2}$ (the Lucas reagent).
3. The test distinguishes alcohols by RATE of formation of alkyl chloride (which appears as TURBIDITY since alkyl chlorides are insoluble in the aqueous reagent).
4. Results:
• 3° alcohol: turbidity APPEARS IMMEDIATELY (carbocation forms easily — tertiary carbocations very stable).
• 2° alcohol: turbidity in ~5–10 minutes.
• 1° alcohol: NO turbidity at room temperature (would need heat).
5. Option B is an oxidising mix (could oxidise alcohols, different test). Options C and D are unrelated chemistry.
_Source: NCERT Class 12 Chemistry Part 2, Ch 7, §7.4 (Distinction of 1°, 2°, 3° alcohols — Lucas test), p. 11._
Related questions
The KOLBE reaction converts phenol (in the form of sodium phenoxide) into salicylic acid. Ethanol reacts with $\mathrm{PCl_5}$ to give which set of products?Phenol reacts with bromine WATER (aqueous $\mathrm{Br_2}$) at room temperature to giveWhen OXIDISED with strong oxidising agents like acidified $\mathrm{KMnO_4}$, the product oThe REIMER-TIEMANN reaction converts phenol to salicylaldehyde. The reagents areThe WILLIAMSON ETHER SYNTHESIS prepares ethers by reactingThe PHENOXIDE ion is more STABLE than the ethoxide ion becauseEthanol heated with concentrated $\mathrm{H_2SO_4}$ at $443\,\text{K}$ (170°C) gives mainl