The product of the reaction between $2-$methyltetrahydrofuran and $HI$ is:

  • A
    $4-$iodopentan$-1-$ol
  • B
    $5-$iodopentan$-2-$ol
  • C
    $1,2-$diiodopentane
  • D
    $1,2-$diiodopentan$-5-$ol

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$A$ mixed ether $(P)$, when heated with excess of hot concentrated hydrogen iodide, produces two different alkyl iodides which when treated with aqueous $NaOH$ give compounds $(Q)$ and $(R)$. Both $(Q)$ and $(R)$ give a yellow precipitate with $NaOI$. Identify the mixed ether $(P)$:

An organic compound $'A'$ $(C_9H_{10}O)$ when treated with conc. $HI$ undergoes cleavage to yield compounds $'B'$ and $'C'$. $'B'$ gives a yellow precipitate with $AgNO_3$ whereas $'C'$ tautomerizes to $'D'$. $'D'$ gives a positive iodoform test. $'A'$ could be :

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