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Benzene diazonium chloride on reaction with phenol in weakly basic medium gives

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Important Questions on Alcohols, Phenols and Ethers

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The increasing order of the pKa values of the following compounds is:
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p-cresol reacts with chloroform in an alkaline medium to give compound A, which adds hydrogen cyanide to form compound B. The latter on acidic hydrolysis gives chiral carboxylic acid. What is the structure of carboxylic acid?
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The major product of the following reaction is:
 

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Arrange the following compounds in order of decreasing acidity :
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In the reaction, the electrophile involved is
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The functional group which is formed when Phenol is made to react with Chloroform in the presence of dilute Sodium hydroxide

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Phenol in presence of sodium hydroxide reacts with chloroform to form salicylaldehyde. The reaction is known as:
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Which of the following compounds will not be soluble in sodium bicarbonate?
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The p-cresol reacts with chloroform in alkaline medium to give the compound A, which adds hydrogen cyanide to form the compound B. The latter, on acidic hydrolysis gives chiral carboxylic acid. The structure of the carboxylic acid is
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Nitrosamines (R2NN=O) are soluble in water. On heating them with concentrated H2SO4, they give secondary amines. What is this reaction called?
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The major product of the following reaction is:

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In the following reaction, the product(s) formed is/are:

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MEDIUM
The acid which contains both -OH and -COOH groups is
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Which one of the following is the most acidic compound?
EASY
Which one of the following substituents at para-position is most effective in stabilizing the phenoxide Question Image ion ?
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What is the product "C" after following reactions -

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What is Z in the following sequence of reactions?
PhenolZn dustXCH3Cl/Anhydrous AlCl3YAlkaline KMnO4Z

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The reactivity of compound Z with different halogens under appropriate conditions is given below:
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The observed pattern of electrophilic substitution can be explained by
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The major product(s) of the following reaction is/are:

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