
10.6: Imines - Chemistry LibreTexts
Recall from section 7.5B that imines have a pKa of approximately 7, so at physiological pH they can be accurately drawn as either protonated (iminium ion form) or neutral (imine). Iminium ion formation: Mechanism (enzymatic): Mechanistically, the formation of an imine involves two steps.
Bordwell pKa Table - Organic Chemistry Data
2017年10月27日 · In short, the stronger the acid, the smaller the pKa value and strong acids have weak conjugate bases. pKa values describe the point where the acid is 50% dissociated (i.e. deprotonated). Below are tables that include determined pKa values for various acids as determined in water, DMSO and in the gas Phase.
7.6: Acid-base properties of nitrogen-containing functional groups
The aromatic compound pyridine, with an imine nitrogen, has a pKa p K a of 5.3. Recall from section 2.2C that the lone pair electrons on the nitrogen atom of pyridine occupy an sp2-hybrid orbital, and are not part of the aromatic sextet - thus, they are available for bonding with a proton.
pKaH of pyridine versus other imines - Chemistry Stack Exchange
Both factors operate in the same direction and tend to make the pyridinium ion (pKa = 5.5 p K a = 5.5) more acidic than the iminium ion (pKa p K a ∼ ∼ 9).
Protonated Imine‐Linked Covalent Organic ... - Wiley Online Library
Protonation of imine-linked COFs yields significant variations of their (opto)electronic properties and results in a largely enhanced performance in photocatalytic hydrogen evolution from water. This is attributed to an enhanced light absorption ability, charge separation efficiency, and hydrophilicity of imine-linked COFs upon protonation.
Imines – Properties, Formation, Reactions, and Mechanisms
2022年3月7日 · Imines are the nitrogen analogues of aldehydes and ketones, containing a C=N bond instead of a C=O bond. They are formed through the addition of a primary amine to an …
H3PO2 H2PO4– HPO4_ H3PO3 H2PO3– H4P2O7 H3 P2O7– H2P2O7= HP2O7= HReO4 HSCN H2SeO3 HSeO3 H2SeO4 HSeO4 H3SiO3 H2SO3 H2SO4 HSO3 HSO4– H2S2O4
Imine - Wikipedia
In organic chemistry, an imine (/ ɪˈmiːn / or / ˈɪmɪn /) is a functional group or organic compound containing a carbon – nitrogen double bond (C=N). The nitrogen atom can be attached to a hydrogen or an organic group (R).
2002年1月16日 · summary Good enantioselective methods for reduction of imines, Strecker reactions, and Mannich reactions exist. Imine alkylations and aza-Diels-Alders are relatively less-developed. In general, imine addition reactions are less well …
What is the pKa value of an imine functional group and how does …
2025年2月7日 · The pKa value of an imine functional group is typically around 9-10. A lower pKa value indicates that the imine is more acidic and therefore more reactive in organic chemistry reactions.