HARD
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Write the mechanism of action of hydrogen bromide on tert-Butyl methyl ether.

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:
HARD
The major product formed in the following reaction is:

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HARD
1-methyl ethylene oxide when treated with an excess of HBr produces
HARD
Write the structures of products formed when anisole is treated with HI.
MEDIUM

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

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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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MEDIUM
Tert-butyl methyl ether on treatment with hydrogen iodide in cold gives
EASY
The heating of phenyl-methyl ether with HI produces,
EASY

Write the structures of the main products in the following reactions:

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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
Methoxy ethane on reaction with hot concentrated HI gives
MEDIUM
Which of the following compounds does NOT react with sodium metal ?
MEDIUM
Major products formed in the reaction of t-butyl methyl ether with HI are -
MEDIUM
Predict the reagent for carrying out the following conversions : 
Anisole to p-bromoanisole
HARD
The acidic hydrolysis of ether (X) shown below is fastest when

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