Tautomer - Search results - Wiki Tautomer
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Tautomers (/ˈtɔːtəmər/) are structural isomers (constitutional isomers) of chemical compounds that readily interconvert. The chemical reaction interconverting... |
Enol (redirect from Keto–enol tautomerism) Examples of keto-enol tautomerism In organic chemistry, alkenols (shortened to enols) are a type of reactive structure or intermediate in organic chemistry... |
interconvert between several structures via lactam-lactim tautomerism. Although the triol tautomer may have aromatic character, the keto form predominates... |
Phosphorous acid (section Nomenclature and tautomerism) exists in equilibrium with an extremely minor tautomer P(OH)3. (In contrast, arsenous acid's major tautomer is the trihydroxy form.) IUPAC recommends that... |
Acetylacetone (section Tautomerism) It exists in equilibrium with a tautomer CH3−C(=O)−CH=C(−OH)−CH3. The mixture is a colorless liquid. These tautomers interconvert so rapidly under most... |
4-Pyridone (section Tautomerism) exists a keto-enol tautomerism with its enol tautomer 4-hydroxypyridine. In solution, the keto tautomer is favoured, and the enol tautomer only becomes important... |
equilibrium with the minor tautomer HP(OH)2. Sometimes the minor tautomer is called hypophosphorous acid and the major tautomer is called phosphinic acid... |
or the enol tautomer. Keto–enol tautomerism is catalyzed by either acid or base. In neutral solution, the enol is the minority tautomer, reversing several... |
solution as a mixture of two tautomers. One tautomer has the proton attached to one of the three oxygen centers. In the second tautomer the proton resides on... |
H−C≡N+−O−. It is an isomer of isocyanic acid (H−N=C=O) and of its elusive tautomer, cyanic acid (H−O−C≡N), and also of isofulminic acid (H−O−N+≡C−). Fulminate... |
shifts in the 1H NMR spectrum. For example, the acidic proton in the enol tautomer of acetylacetone appears at δ H {\displaystyle \delta _{\text{H}}} 15... |
toward hydroxide. Because the triaminobenzene also exists as its imine tautomer, it is susceptible to hydrolysis. Phloroglucinol is a weak triprotic acid... |
or N3-H tautomers. The N3-H tautomer is shown in the figure above. In the N1-H tautomer, the NH is nearer the backbone. These neutral tautomers, also referred... |
Alkynol (section Ynol–ketene tautomerism) with ketenes, much like enols can with aldehydes and ketones. The ynol tautomer is usually unstable, does not survive long, and changes into the ketene... |
any molecule that contains the -C(=NH)-OH functional group. It is the tautomer of an amide and the isomer of an oxime. The term "imino acid" is an obsolete... |
2-Pyridone (section Tautomerism) case of a compound that exists as tautomers. The second tautomer is 2-hydroxypyridine. This lactam lactim tautomerism can also be exhibited in many related... |
structure H−S−C≡N, which exists as a tautomer with isothiocyanic acid (H−N=C=S). The isothiocyanic acid tautomer tends to dominate with the compound being... |
class of molecules, purines, which include substituted purines and their tautomers. They are the most widely occurring nitrogen-containing heterocycles in... |
acedianthrone, a useful octacyclic pigment. Anthrone is the more stable tautomer relative to the anthrol. The tautomeric equilibrium is estimated at 100... |
pyrrole derivatives fused to a butadiene. In solution, the 2H-isoindole tautomer predominates. It resembles a pyrrole more than a simple imine. The degree... |