pyridine वाक्य
उदाहरण वाक्य
मोबाइल
- Pyridine was discovered in 1849 by the Scottish chemist bone oil.
- The chemical structure of pyridine was determined decades after its discovery.
- Pyridine is readily degraded by bacteria to ammonia and carbon dioxide.
- The reaction is catalysed with weak base like piperidine or pyridine.
- The balanced chemical equation, using methanol and pyridine, is:
- Pyridine is nitrated to 3-nitropyridine and 4-nitropyridine.
- Included are pyridine, thiophene, pyrrole, and furan.
- Electron lone pair availability ( basicity ) is decreased compared to pyridine.
- Pyridine is conventionally detected by the gas chromatography and mass spectrometry methods.
- The nitrogen center of pyridine features a basic lone pair of electrons.
- The pyridine ligand replaced during the reaction is restored after its completion.
- Pyridine is harmful if inhaled, swallowed or absorbed through the skin.
- Pyridine might also have minor genotoxic, and clastogenic effects.
- Like the related molecule pyridine and quinoline, acridine is mildly basic.
- Typical examples of basic aromatic rings are pyridine or quinoline.
- With pyridine as a base and solvent, refluxing conditions are required.
- Examples include pyridine, phosphabenzene, arsabenzene, and pyrylium.
- Bases such as pyridine can also be used to promote the reaction:
- Copper hydride reversibly precipitates from pyridine solution, as an amorphous solid.
- Pyridine itself is a relatively weak ligand in forming quantitative analysis of iron.
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