Advertisements
Advertisements
प्रश्न
Predict the product of the following reaction:
\[\ce{CH3 - CH2 - CH2 - O - CH3 + HBr ->}\]
Advertisements
उत्तर
Both the alkyl groups attached to oxygen are primary, so the Br− ion will react with the smaller alkyl group (methyl group) to form propan-1-ol and bromomethane.
\[\ce{\underset{n-propyl methyl ether}{CH3 - CH2 - CH2 - O - CH3} + HBr ->[373 K] \underset{propan-1-ol}{CH3 - CH2 - CH2 - OH} + \underset{bromomethane}{CH3Br}}\]
APPEARS IN
संबंधित प्रश्न
Write the main product(s) in each of the following reactions:
Predict the product of the following reaction:
\[\ce{(CH3)3C - OC2H5 ->[HI]}\]
Show how will you synthesize cyclohexylmethanol using an alkyl halide by an SN2 reaction.
Write the equation of the reaction of hydrogen iodide with 1-propoxypropane.
Write the equation of the reaction of hydrogen iodide with methoxybenzene.
Write the equation of the reaction of hydrogen iodide with benzyl ethyl ether.
Explain the fact that in aryl alkyl ethers
- the alkoxy group activates the benzene ring towards electrophilic substitution and
- it directs the incoming substituents to ortho and para positions in the benzene ring.
Write the mechanism of the reaction of HI with methoxymethane.
Write the product(s) in the following reaction
Write the formula of reagents used in the following reactions :
Bromination of phenol to 2,4,6-tribromophenol
Write the structures of the main products in the following reactions :
The ether
when treated with HI produces:
Maximum number of H-bonds that can be formed by a water molecule is
Indicate the σ and π bond in the following molecule:
HCONHCH3
