Chemistry - ALCOHOL & ETHER Question with Solution | TestHub

ChemistryALCOHOL & ETHEROXIDATION OF ORGANIC COPMOUNDSMedium2 minQB
ChemistryMediumsingle choice

image.png

P will be :

Options:

Answer:
A
Solution:

Question Explanation:

The question asks for the product P formed when a cyclic triol reacts with .

Concept:

This question is based on oxidative cleavage of vicinal diols.

Solution:

Periodic acid ( ) selectively cleaves the bond of vicinal diols (adjacent - OH groups). This cleavage forms carbonyl compounds.

In the given molecule, the -OH groups at positions 1 and 2 are vicinal.

The -OH at position 4 is isolated and does not react.

Cleavage of the C1-C2 bond occurs.

The secondary alcohols at C1 & C2 are converted into an aldehyde.

image.png

Stream:JEESubject:ChemistryTopic:ALCOHOL & ETHERSubtopic:OXIDATION OF ORGANIC COPMOUNDS
2mℹ️ Source: QB

Doubts & Discussion

Loading discussions...