Chemistry - ALCOHOL & ETHER Question with Solution | TestHub
ChemistryALCOHOL & ETHEROXIDATION OF ORGANIC COPMOUNDSMedium2 minQB
ChemistryMediumsingle choice
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.
Stream:JEESubject:ChemistryTopic:ALCOHOL & ETHERSubtopic:OXIDATION OF ORGANIC COPMOUNDS
⏱ 2mℹ️ Source: QB
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