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Q: How can you convert furan to pyridine?
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Related questions

Preparation of 3-hydroxy pyridine?

Try reacting furan-2-aldehyde with ammonia in ethanol


Why do 5-membered ring aromatic heterocycles pyrrole and furan undergo electrophilic substitution more rapidly than benzene while 6-membered ring heterocycles like pyridine are less reactive than Benz?

pyridine is less reactive than benzene because when we form its conjugate base then it'll b more stable than dat of benzene.. so more stabler means less reactive.......and also due to more resonance in benzene it will b more reactive...same 4 furan and pyrrole


Why furan do not show nucleophilic subtitution reaction?

Hi I m confused that in simple furan why it do not show nucleophilic subtitution reaction. while in subtituted furan show it.


What are pyridine bases?

Bases containing the pyridine substructure, or derived from pyridine as a starting material. Pyridine is basically benzene with one of the carbons substituted with a nitrogen, if that helps.


Is pyridine is a tertiary amine?

Yes Pyridine is a tertiary amine.


Can sodium chloride be solved in pyridine?

NaCl is not soluble in pyridine.


What is the use of pyridine free reagent in Karl fischer?

because pyridine is toxic...so amines are used in place of pyridine.......


Why pyridine is used im the synthesis of aspIrin?

pyridine is a base it accept hydrogen and forms pyridine hydrochloride in the synthesis of Aspirin


How many moles of pyridine are contained in 3.13 g of pyridine?

0.0396


What is the products obtained when pyridine reacts with sodamide?

2-amino pyridine derivates by the reaction of pyridine with sodium amide and this reaction called chichibabinrection


What is the reaction between pcl5 and pyridine?

experimental of reaction between pyridine and PCl5


What product contains Pyridine?

Certain denatured alcohols might contain pyridine; it's used to make the ethanol undrinkable (pyridine has an unpleasant fishy odor and taste).