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The term "imine" was coined in 1883 by the German chemist Albert Ladenburg. [6] Usually imines refer to compounds with the general formula R 2 C=NR, as discussed below. [7] In the older literature, imine refers to the aza-analogue of an epoxide. Thus, ethylenimine is the three-membered ring species aziridine C 2 H 4 NH. [8]
A general linear imide functional group. In organic chemistry, an imide is a functional group consisting of two acyl groups bound to nitrogen. [1] The compounds are structurally related to acid anhydrides, although imides are more resistant to hydrolysis.
Ethanimine is an organonitrogen compound classified as an imine. It is formed by reacting acetaldehyde and ammonia, but rapidly polymerizes to acetaldehyde ammonia trimer. It has two tautomers: ethanimine, an imine, and ethenamine or aminoethylene, an amine. Ethanimine has two hydrogens on the carbon, while ethenamine has two on the nitrogen atom.
The ideal gas equation can be rearranged to give an expression for the molar volume of an ideal gas: = = Hence, for a given temperature and pressure, the molar volume is the same for all ideal gases and is based on the gas constant: R = 8.314 462 618 153 24 m 3 ⋅Pa⋅K −1 ⋅mol −1, or about 8.205 736 608 095 96 × 10 −5 m 3 ⋅atm⋅K ...
P water S = Partial pressure of water in saturated air (that is, at 100% relative humidity; in this case the partial pressure is equal to the vapour pressure, which can be determined as a function of ambient temperature) P water B = Partial pressure of water in saturated air in 37 °C = 47 mmHg; T S = Standard temperature in kelvins (K) = 273 K
Methylene imine is an organic compound with the chemical formula H 2 C=NH. The simplest imine , it is a stable, colorless gas that has been detected throughout the universe. [ 1 ] Structural parameters determined by microwave spectroscopy include a C=N bond length of 1.27 Å , an N–H bond length of 1.02 Å and an H−N=C bond angle of 110.5 ...
Diimines are prepared by condensation reactions where a dialdehyde or diketone is treated with amine and water is eliminated. [2] Many are derived from the condensation of 1,2-diketones and dialdehydes with amines, often anilines. [3] The dialdehyde glyoxal is an especially common precursor. Similar methods are used to prepare Schiff bases and ...
In organic chemistry, an oxime is an organic compound belonging to the imines, with the general formula RR’C=N−OH, where R is an organic side-chain and R' may be hydrogen, forming an aldoxime, or another organic group, forming a ketoxime. O-substituted oximes form a closely related family of compounds.