When methoxybenzene reacts with HI at room te | vedclass

Name: Exam Paper Generator | JEE NEET Paper Generator | Vedclass
Brand: Vedclass
Rating: 5 (35 reviews)

Question

(B) The reaction of methoxybenzene $(C_6H_5OCH_3)$ with $HI$ involves the cleavage of the $C-O$ bond. In aryl alkyl ethers,the $O-CH_3$ bond is weaker

Vedclass · Accepted Answer

Iodomethane and Phenol

Vedclass · Answer

(B) The reaction of methoxybenzene $(C_6H_5OCH_3)$ with $HI$ involves the cleavage of the $C-O$ bond. In aryl alkyl ethers,the $O-CH_3$ bond is weaker than the $O-C_6H_5$ bond because the $O-C_6H_5$ bond has partial double bond character due to resonance. Therefore,the $HI$ attacks the methyl group,resulting in the formation of phenol $(C_6H_5OH)$ and iodomethane $(CH_3I)$. The reaction is: $C_6H_5OCH_3 + HI \rightarrow C_6H_5OH + CH_3I$.

When methoxybenzene reacts with $HI$ at room temperature,the products formed are:

Similar Questions

Which of the following will not give ether as a product?

The major product of the above reaction is:

When alkyl halide is heated with dry $Ag_2O$,it produces

In which of the following reactions is the product an ether?

For the reaction shown below,identify products $A$ and $B$ $:$

Vedclass Test Series

Exam Paper Generator

Online Exam Module