The products $(A)$ and $(B)$ of the above reaction are:

Which of the following is the correct order of reactivity for:

Among the given compounds,the correct order of enol content is:
$(I)$ Cyclopentanone
$(II)$ $4$-hydroxycyclopent-$2$-en-$1$-one derivative
$(III)$ $\gamma$-butyrolactone derivative

The most likely protonation site in the following molecule is:

In the above reaction,the electrophile is substituted at the meta position only,due to:
$I$. Electron density is more at ortho $\&$ para positions
$II$. Electron density is relatively less at ortho $\&$ para positions
$III$. Electron density is less at meta position
$IV$. Electron density is relatively more at meta position
The correct answer is:

Heterolysis of $C-Cl$ bond produces: