keto form वाक्य
उदाहरण वाक्य
मोबाइल
- The enol and keto forms are said to be tautomers of each other.
- It is a tautomeric compound existing in enolic form in organic solvents and as a keto form in water.
- This prevents opening of the chain to the aldehyde or keto form and renders the modified residue non-reducing.
- With much of the literature on the synthesis of quinolines, there is some discrepancy on whether keto form ) predominates.
- However, 5, 5-dimethyloxyluciferin emits green light even though it is constricted to the keto form because it cannot tautomerize.
- In protic solvents, the equilibrium lies towards the keto form as the intramolecular hydrogen bond competes with hydrogen bonds originating from the solvent.
- The mechanism suggests that red light is emitted from the keto form of oxyluciferin, while green light is emitted from the enol form of oxyluciferin.
- Normally, the keto enol tautomerization chemical equilibrium is highly thermodynamically driven, and at room temperature the equilibrium heavily favors the formation of the keto form.
- A reducing end of a carbohydrate is a carbon atom that can be in equilibrium with the open-chain aldehyde ( aldose ) or keto form ( ketose ).
- The keto form ( shown in the infobox ) is complementary to adenine, so it can be incorporated into DNA by aligning opposite adenine residues during DNA replication ( see below left ).
- A classic example for favoring the keto form can be seen in the equilibrium between vinyl alcohol and acetaldehyde ( K = [ enol ] / [ keto ] H " 3 ?10 " 7 ).
- Also, when it is irradiated with UVA light, it generates a triplet excited state in the keto form which can either cause the avobenzone to degrade or it can transfer energy to biological targets and cause deleterious effects.
- A compound containing a carbonyl group ( C = O ) is normally in rapid equilibrium with an enol tautomer, which contains a pair of doubly bonded carbon atoms adjacent to a hydroxyl ( " OH ) group, C = C-OH . The keto form predominates at equilibrium for most ketones.
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