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Pyridine itself (unsubstituted) is basic due to presence of lone pare of electron on nitrogen atom which is not involved in aromatic character , methyl at 4th (Para) position is electron donor due to hyper-conjugation so electrons density at nitrogen becomes increase so 4-methyl pyridine is more basic as compare to unsubstituted pyridine.
because pyridine is toxic...so amines are used in place of pyridine.......
pyridine is a base it accept hydrogen and forms pyridine hydrochloride in the synthesis of Aspirin
2-amino pyridine derivates by the reaction of pyridine with sodium amide and this reaction called chichibabinrection
experimental of reaction between pyridine and PCl5
what is the reaction mechanism between acrylic acid,4-vinyl pyridine
Pyridine itself (unsubstituted) is basic due to presence of lone pare of electron on nitrogen atom which is not involved in aromatic character , methyl at 4th (Para) position is electron donor due to hyper-conjugation so electrons density at nitrogen becomes increase so 4-methyl pyridine is more basic as compare to unsubstituted pyridine.
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.
Yes Pyridine is a tertiary amine.
NaCl is not soluble in pyridine.
because pyridine is toxic...so amines are used in place of pyridine.......
pyridine is a base it accept hydrogen and forms pyridine hydrochloride in the synthesis of Aspirin
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2-amino pyridine derivates by the reaction of pyridine with sodium amide and this reaction called chichibabinrection
experimental of reaction between pyridine and PCl5
Certain denatured alcohols might contain pyridine; it's used to make the ethanol undrinkable (pyridine has an unpleasant fishy odor and taste).
In the related links box below, I posted the wikipedia article on pyridine acid.