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Acidic strength of the four phenols should be:
(a)-methylphenol > Phenol -Nitrophenol - Nitrophenol
(b)-methylphenol -
nitrophenol phenol -
nitrophenol
nitrophenol phenol -
nitrophenol
(c)-methylphenol phenol -nitrophenol - nitrophenol
(d)phenol -methylphenol -nitrophenol - nitrophenol.

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Important Questions on Alcohols, Phenols and Ethers
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Correct increasing order of acidity is as follows:

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How can phenol and benzoic acid be distinguished?

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Why is the ionization constant of phenol is higher than that of ethanol?

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Phenol reacts with bromine in carbon disulphide at low temperature to give:

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-cresol reacts with chloroform in alkaline medium to give compound which adds to form The latter on acidic hydrolysis gives chiral carboxylic acid. What is the structure of carboxylic acid?

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Reimer-Tiemann reaction involves:

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When phenol is treated with excess bromine water, what does it give?

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When phenol is reacted with and followed by acidification, salicylaldehyde is obtained. Which of the following species are involved in the above mentioned reaction as intermediates?
