In the nucleophilic addition of CN^- to carbonyl carbon, the intermediate formed is

Tetrahedral

Right on! Give the BNAT exam to get a 100% scholarship for BYJUS courses

Planar

No worries! We‘ve got your back. Try BYJU‘S free classes today!

Cyclic

No worries! We‘ve got your back. Try BYJU‘S free classes today!

Pyramidal

No worries! We‘ve got your back. Try BYJU‘S free classes today!

Open in App

Solution

The correct option is A
Tetrahedral

With addition of CN^-to carbonyl carbon, hybridisation changes from sp²(planar) to sp³(tetrahedral).

Suggest Corrections

Similar questions

In the nucleophilic addition of CN^-1 to carbonyl compound the intermediate formed is

The most characteristic reaction of aldehyde and ketones is nucleophilic addition to carbon oxygen double bond. Aldehyde and ketones are easily susceptible to nucleophilic addition because of structural features. The trigonal planar arrangement of groups around the carbonyl carbon atom means that the carbonyl carbon atom is relatively open to attack from above and below the plane of carbonyl group. The partial positive charge on the carbonyl atom means that it is especially susceptible to attack by a nucleophile

Oximes are formed by the reaction of aldehyde or ketones with

Q. The nucleophilic addition at the carbonyl carbon changes its hybridization fromto

Q. Choose the correct order of alkyl group attached to aldehyde that prefer the nucleophilic addition at carbonyl carbon?

Join BYJU'S Learning Program

In the nucleophilic addition of CN- to carbonyl carbon, the intermediate formed is

The correct option is A Tetrahedral With addition of CN- to carbonyl carbon, hybridisation changes from sp2(planar) to sp3 (tetrahedral).

In the nucleophilic addition of CN^- to carbonyl carbon, the intermediate formed is

The correct option is A
Tetrahedral

With addition of CN^-to carbonyl carbon, hybridisation changes from sp²(planar) to sp³(tetrahedral).