Identify the site,where attack of $H^{+}$ is most favourable.

  • A
    $a$
  • B
    $b$
  • C
    $c$
  • D
    $d$

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The correct stability order of the given canonical structures is:

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Correct statements for the given reaction are :
$A$. Compound '$B$' is aromatic
$B$. The completion of above reaction is very slow
$C$. '$A$' shows tautomerism
$D$. The bond lengths $C-C$ in compound $B$ are found to be same
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Which of the following is the most unstable resonating structure?

Arrange the following in the decreasing order of stability:
$I. CH_2=CH-CHO$
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$III. ^-CH_2-CH=CH-O^+$

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