Compare the carbon-carbon double bond rotation energy for the following compounds $A$,$B$,and $C$:

  • A
    $A > B > C$
  • B
    $A > C > B$
  • C
    $B > A > C$
  • D
    $B > C > A$

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Compare the ease of carbon-carbon bond rotation across $A, B,$ and $C$.

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The order of relative stability of the contributing structures is:
$I: CH_2=CH-CHO$
$II: ^+CH_2-CH=CH-O^-$
$III: ^-CH_2-CH=CH-O^+$
Choose the correct answer from the options given below:

Which of the following is the least stable?

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Which of the following species does not exert a resonance effect?

Which of the following is not a resonating structure of others?

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