Step 1: Understanding the given structure. The given compound contains a hydroxyl (-OH) group attached to a tertiary carbon in a cyclic structure. This suggests the presence of a tertiary alcohol.
Step 2: Understanding the given tests. - \(Br_{2}\) water test: Used to detect unsaturation (double bonds) or phenols. The given compound does not contain a double bond or a phenol group.
- Tollen’s test: Used to detect aldehydes and alpha-hydroxy ketones. The given compound is not an aldehyde or an alpha-hydroxy ketone.
- Victor Meyer test: Used to distinguish between primary, secondary, and tertiary alcohols, but it does not confirm the presence of a tertiary alcohol directly.
- Lucas test: Used to differentiate between primary, secondary, and tertiary alcohols. Since tertiary alcohols react immediately, this test is suitable for the given compound.
Step 3: Identifying the correct test. Since the compound is a tertiary alcohol, it reacts instantly with Lucas reagent (\(ZnCl_{2}/HCl)\), forming a cloudy solution due to the formation of an alkyl chloride.
Final Answer: The given compound gives a positive Lucas test, confirming the presence of a tertiary alcohol.
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 |