Noun:

আমি খনি,

imines's Usage Examples:

relationship of imines to amines having double and single bonds carries over to imides and amides, as in acetamide vs succinimide.

They can be considered a sub-class of imines, being either secondary ketimines or secondary aldimines depending on their.

N-Sulfinyl imines (N-sulfinylimines, sulfinimines, thiooxime S-oxides) are a class of imines bearing a sulfinyl group attached to nitrogen.

These imines display.

(N2O) Nitrones (R2CN(R)O) Some imines: Azomethine imine Nitrilimines (RCN-NR, analogous to nitrile oxide) Carbonyl imines Some ylides Azomethine ylide Nitrile.

Diimines are organic compounds containing two imine (RCH=NR') groups.

Common derivatives are 1,2-diketones and 1,3-diimines.

the thus produced highly reactive ketenes with suitable reagents such as imines, amines, or alcohols.

Primary amines react with ketones and aldehydes to form imines.

2H-Azirines can be considered strained imines and are isolable.

In organic chemistry, a semicarbazone is a derivative of imines formed by a condensation reaction between a ketone or aldehyde and semicarbazide.

α-methylene carbonyls are also considered Mannich reactions because these imines form between amines and aldehydes.

An oxime is a chemical compound belonging to the imines, with the general formula RR'C=NOH, where R is an organic side-chain and R' may be hydrogen, forming.