CBSE Class 12-science Answered
how is the cabonyl group of aldehyde/ketone affected in the presence of electron donating group like metyl in cyanohydrin reaction?
Asked by prakriti12oct | 14 Feb, 2020, 12:09: PM
Expert Answer
(a) Formation of cyanohydrins:
- On addition of HCN to aldehydes and ketones they yield cyanohydrins.
- Since the reaction is very slow with pure HCN, it is catalysed with the help of a base and the cyanide ion (CN-) generated as a strong nucleophile adds to carbonyl compounds to give cyanohydrins.
- The C-O double bond is polarised since oxygen is electronegative than carbon.
- So the carbonyl carbon is an electrophilic centre and the carbonyl oxygen is a nucleophilic centre.
- If an electron donating group is present next to carbonyl group then it will slow down the reaction or will retard the rate of reaction.
Answered by Ramandeep | 14 Feb, 2020, 05:57: PM
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