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Phenyl methyl ether (anisole) reacts with HI to give Phenol and methyl iodide and not iodobenzene and methyl alcohol because

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Important Questions on Alcohols, Phenols and Ethers

MEDIUM
An organic compound 'AC9H10O when treated with conc. HI undergoes cleavage to yield compound 'B' and 'C'. 'B' gives yellow precipitate with AgNO3 where as 'C' tautomerizes to 'D'. 'D' gives positive iodoform test. 'A' could be:
MEDIUM

The major product [B] in the following reaction is :

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EASY
Methoxy ethane on reaction with hot concentrated HI gives
HARD
The major product formed in the following reaction is:

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EASY
One mole of an organic compound A with the formula C3H8O reacts completely with two moles of HI to form X and Y. When Y is boiled with aqueous alkali it forms Z. Z answers the iodoform test. The compound A is
HARD

The major aromatic product C in the following reaction sequence will be :

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EASY
Which reaction is used in Zeisel's method of detection and estimation of alkoxy group?
HARD
The acidic hydrolysis of ether (X) shown below is fastest when

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MEDIUM
The major product of the following reaction is:
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EASY

What are the products formed in the following reaction?

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EASY
The heating of phenyl-methyl ether with HI produces,
MEDIUM
Which of the following compounds does NOT react with sodium metal ?
MEDIUM
Main Products formed during a reaction of 1-methoxy naphthalene with hydroiodic acid are:
HARD
1-methyl ethylene oxide when treated with an excess of HBr produces
MEDIUM
Major products formed in the reaction of t-butyl methyl ether with HI are -
MEDIUM
Tert-butyl methyl ether on treatment with hydrogen iodide in cold gives