Which of the following ethers will undergo electrophilic substitution reaction?

  • A
    $CH_3OC_2H_5$
  • B
    $C_6H_5OCH_3$
  • C
    $CH_3OCH_3$
  • D
    $C_2H_5-O-C_2H_5$

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The compound $CH_3-O-C(CH_3)_3$ is prepared best by the reaction:

An organic compound with the molecular formula $C_4H_{10}O$ does not react with sodium metal. Upon reaction with excess $HI$,it yields only two types of halides. Identify the compound.

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In the reaction $CH_3-CH(CH_3)-CH_2-O-CH_2-CH_3 + HI \xrightarrow{\text{Heated}} \dots$,which of the following compounds will be formed?

Which of the reactants given below is/are suitable for the preparation of Methoxybenzene?
$(x)$ $C_6H_5Br + CH_3ONa$
$(y)$ $C_6H_5ONa + CH_3Br$

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Assertion : Iodide ion combines with smaller group to avoid steric hindrance.
Reason : With $HI$,anisole gives iodobenzene and methyl alcohol.

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