please tell theorder of acidity for the above compounds with example
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I think it's a resonance structure of ortho ,mata and para position .
m-cresol is the more acidic than p-cresol,, because in ortho and para isomers, hyperconjugative effects of -CH3 group lead to an increase in electron density on the oxygen atom. that's why C>D.
group in o-cresol produces +I-effect which decreases the polarity due to increase in electron density on —OH bond. So, o-cresol is a weaker acid than phenol. Thus, the correct order is o-cresol < phenol
yes it's A>C>D>B.
i hope it helps you bro .
good question also for me ..!!!
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