One mole of an organic compound $(A)$ with the formula $C_3H_8O$ 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

  • A
    Propan$-1-$ol
  • B
    Propan$-2-$ol
  • C
    Ethoxy ethane
  • D
    Methoxy ethane

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Similar Questions

Which of the following aromatic ethers does not undergo cleavage by $HI$ at $525 \ K$?

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The following are possible syntheses of phenyl propyl ether. Which one would work?
$(i)$ $C_6H_5OH$ $\xrightarrow{KNH_2}$ $\xrightarrow{CH_3CH_2CH_2Br}$
(ii) $CH_3CH_2CH_2OH$ $\xrightarrow{NaOH}$ $\xrightarrow{C_6H_5Br}$
(iii) $CH_3CH_2CH_2OH$ $\xrightarrow{NaH}$ $\xrightarrow{C_6H_5Br}$

The $C - O - C$ bond angle in ethers is approximately -

The bond angle of $C-O-C$ bond in methoxy methane is (in $^{\circ}$)

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

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