| 1. | Keto-enol tautomerism is catalyzed by either acid or base.
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| 2. | In keto-enol tautomerism, thioenols interconvert with thioketones or thioaldehydes.
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| 3. | It is stable and does show keto enol tautomerism.
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| 4. | Then, keto-enol tautomerism occurs, resulting in the desired product.
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| 5. | The Keto-enol tautomerism strongly depends on the solvent used for the experiments.
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| 6. | The enamine-imine tautomerism may be considered analogous to the keto-enol tautomerism.
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| 7. | The enamine-imine tautomerism may be considered analogous to the keto-enol tautomerism.
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| 8. | This lactam lactim tautomerism can also be found in other molecules with a similar structure.
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| 9. | This is called keto-enol tautomerism.
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| 10. | Certain triazoles are relatively easy to cleave due to so-called ring-chain tautomerism.
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