What is the increasing order of boiling points for the following alcohols?
$I.$ $1, 2-$dihydroxybenzene
$II.$ $1, 3-$dihydroxybenzene
$III.$ $1, 4-$dihydroxybenzene
$IV.$ hydroxybenzene

  • A
    $I < II < IV < III$
  • B
    $I < II < III < IV$
  • C
    $IV < I < II < III$
  • D
    $IV < I < III < II$

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The correct order of acidity of the above compounds is:

Which of the following will be most easily attacked by an electrophile?

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What is the product formed when phenol reacts with $Br_2$ in $CCl_4$ at low temperature?

Difficult
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Assertion : Phenol is a stronger acid than ethanol.
Reason : Groups with $+M$ effect decrease acidity at $p-$position.

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