Organic Chemistry
Resonance in benzene is accompanied by delocalization of $$\pi$$ electrons. Each $$\pi$$ electron is attached with
Which one of the following groups can exert both $$+ M$$ and $$- I$$ effect?
Inductive effect is an electronic effect due to the polarisation of $$\sigma$$ bonds within a molecule or ion. It is mainly due to the electronegativity difference between the atoms on either side of the bond. $$Cl$$ atom exerts $$-I$$ effect as it is highly electronegative in nature and therefore, withdraws electron density. However, due to the presence of lone pair of electrons on it, it can also donate electron density leading to various resonating structures in aromatic compounds. This effect is known as $$+M$$ effect.
Hence, $$-Cl$$ group can exert both $$-I$$ and $$+M$$ effect.
Resonance in benzene is accompanied by delocalization of $$\pi$$ electrons. Each $$\pi$$ electron is attached with
In benzene, all the C- C bonds have the same length because of_________.
Which of the following functional group shows $$+R$$ effect?
The correct order of stability for the given alkoxides is :
The "N" which does not contribute to the basicity for the compound is :
The correct stability order of the following resonance structures is: $$\underset{(I)}{H_2C=\overset{+}{N}=\overset{-}{N}}$$ $$\underset{(II)}{H_2\overset{+}{C}-N=\overset{-}{N}}$$ $$\underset{(III)}{H_2\overset{-}{C}-\overset{+}{N}\equiv N}$$ $$\underset{(IV)}{H_2\overset{-}{C}-N=\overset{+}{N}}$$
Which of the following group is sharp ortho and para directive?
The order of leaving group ability is : i. $$-OAc$$ ii. $$-OMe$$ iii. $$-OSO_4Me$$ iv. $$-OSO_2CF_3$$
Among the following, the least stable resonance structure is :
Which of the following have +M effect ($$\bar { e }$$-donating mesomeric effect) ?