In the following reaction,compound $Q$ is obtained from compound $P$ via an ionic intermediate. What is the degree of unsaturation of $Q$?

For the given molecule,$x$,the preferred site for the attack of the electrophile is:

What are the main types of organic reactions and their mechanisms?

Which of the following orders is correct?

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:

Which of the following represent free radical substitution reaction $(FSR)$,electrophilic addition reaction $(EAR)$ and nucleophilic addition reaction $(NAR)$?
$I. CH_3-CH=CH_2 \xrightarrow{Cl_2/CCl_4} CH_3-CHCl-CH_2Cl$
$II. CH_3-CO-CH_3 \xrightarrow{HCN/OH^-} CH_3-C(OH)(CN)-CH_3$
$III. CH_3-CH_2-CH_3 \xrightarrow{Cl_2/h\nu} CH_3-CHCl-CH_3$