An ether $(A)$,$C_5H_{12}O$,when heated with excess of hot concentrated $HI$ produced two alkyl halides which when treated with $NaOH$ yielded compounds $(B)$ and $(C)$. Oxidation of $(B)$ and $(C)$ gave a propanone and an ethanoic acid respectively. The $IUPAC$ name of the ether $(A)$ is

  • A
    $2-$ethoxypropane
  • B
    ethoxypropane
  • C
    methoxybutane
  • D
    $2-$methoxybutane

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On boiling with concentrated hydrobromic acid,phenyl ethyl ether will yield:

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$(i)$ $CH_3-CH_2-CH(CH_3)-CH_2-O-CH_2-CH_3$
$(ii)$ $CH_3-CH_2-CH_2-O-C(CH_3)_2-CH_2-CH_3$
$(iii)$ $C_6H_5-CH_2-O-C_6H_5$

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