Hydrogenation of naphthalene $(P)$ with excess hydrogen gas stops cleanly at $1, 2, 3, 4-$ tetrahydronaphthalene $(Q).$ What conclusion can be drawn from this experiment?

  • A
    the hydrogenation of $P$ is exothermic
  • B
    one aromatic ring of $P$ is more reactive than the aromatic ring of $Q$
  • C
    one aromatic ring of $P$ is less reactive than the other ring of $Q$
  • D
    reduction of the first $C=C$ of $P$ is faster than reduction of the second or third $C=C$

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