
Step 1: Structure Analysis. The compound features a hydroxyl (-OH) group attached to a tertiary carbon within a cyclic system, indicating a tertiary alcohol.
Step 2: Test Analysis.
- Bromine water test (\(Br_{2}\) water): Detects unsaturation or phenols. The compound lacks these functional groups.
- Tollen's test: Identifies aldehydes and alpha-hydroxy ketones. The compound is neither.
- Victor Meyer test: Differentiates primary, secondary, and tertiary alcohols, but does not confirm tertiary alcohols directly.
- Lucas test: Distinguishes primary, secondary, and tertiary alcohols. Tertiary alcohols react instantaneously, making this test appropriate.
Step 3: Test Selection. As a tertiary alcohol, the compound will react immediately with Lucas reagent (\(ZnCl_{2}/HCl\)), producing a cloudy alkyl chloride solution.
Final Answer: The compound yields a positive Lucas test, verifying its tertiary alcohol nature.
Why is \( Cr^{2+} \) strongly reducing while \( Mn^{3+} \) is strongly oxidizing?
| List - I(Block/group in periodic table) | List - II(Element) |
|---|---|
| (A) Lanthanoid | (I) Ce |
| (B) d-block element | (II) As |
| (C) p-block element | (III) Cs |
| (D) s-block element | (IV) Mn |