Which of the following statements are not correct?
$a$. The energy of resonance hybrid structure is higher than that of the possible canonical structures of the molecule.
$b$. When inductive effect and electromeric effect operate in opposite directions,electromeric effect predominates.
$c$. When the $\pi$ electrons of the multiple bond are transferred to that atom to which the attacking reagent does not get attached,it is known as $+E$ effect.
$d$. The resonance structures with separation of opposite charges are more stable.

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

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The decreasing order of acidity of the following terminal acetylenes is:

Which of the following statements are $TRUE$?
$(I)$ Inductive effect operates through the $\sigma$ bond
$(II)$ Resonance effect operates through the $\pi$ bond
$(III)$ Inductive effects operate through the $\pi$ bond
$(IV)$ Resonance effect operates through the $\sigma$ bond

In the compound given below,the correct order of the acidity of the positions $(X)$,$(Y)$ and $(Z)$ is:

Which of the following molecule$(s)$ has/have delocalised lone pair$(s)$ of electrons?

Which one of the following is not true regarding electromeric effect?

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