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An acyclic hydrocarbon $P$ , having molecular formula $C_{6} H_{10}$ , gave acetone as the only organic product through the following sequence of reactions, in which $Q$ is an intermediate organic compound. The structure of the compound $Q$ is:

$(C H_{3})_{2} C H C H (O H) C H_{2} C H_{3}$
$(C H_{3})_{3} C C H (O H) C H_{3}$
$(C H_{3})_{2} C H C H_{2} C H (O H) C H_{3}$
$C H_{3} C H_{2} C H_{2} (O H) C H C H_{2} C H_{3}$

A

(C H_{3})_{2} C H C H (O H) C H_{2} C H_{3}

B

(C H_{3})_{2} C H C H_{2} C H (O H) C H_{3}

C

(C H_{3})_{3} C C H (O H) C H_{3}

D

C H_{3} C H_{2} C H_{2} (O H) C H C H_{2} C H_{3}

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