(i) C6H6
There are six C-C sigma (σ C-C) bonds, six C–H sigma (σ C-H) bonds, and three C=C pi (𝜋𝐶−𝐶) resonating bonds in the given compound.
(ii) ) C6Hl2
There are six C-C sigma (σ C-C) bonds and twelve C-H sigma (σ C-H) bonds in the given compound.
(iii) CH2Cl2
There are two C-H sigma (σ C-H) bonds and two C-Cl sigma (σ C-Cl) bonds in the given compound.
(iv) CH2 = C = CH
There are two C-C sigma (σ C-C) bonds, four C-H sigma (σ C-H ) bonds, and two C=C pi (σ C-C) bonds in the given compound.
(v) CH3NO2
There are three C-H sigma (σ C-H) bonds, one C-N sigma (σ C-N) bond, one N-O sigma (σ N-O) bond, and one N=O PI(π N=O) bond in the given compound.
(vi) HCONHCH3
There are two C-N sigma (σ C-N) bonds, four C-H sigma (σ C-H) bonds, one N-H sigma bond, and one C=O pi (π C-C) bond in the given compound.


Find the mean deviation about the mean for the data 38, 70, 48, 40, 42, 55, 63, 46, 54, 44.
SN1 reaction mechanism takes place by following three steps –
The SN2 reaction mechanism involves the nucleophilic substitution reaction of the leaving group (which generally consists of halide groups or other electron-withdrawing groups) with a nucleophile in a given organic compound.
The mechanism of an electrophilic aromatic substitution reaction contains three main components which are:
The electrophilic substitution reaction mechanism is composed of three steps, which will be discussed more below.