Organic Chemistry
Resonance in benzene is accompanied by delocalization of $$\pi$$ electrons. Each $$\pi$$ electron is attached with
The order of leaving group ability is : i. $$-OAc$$ ii. $$-OMe$$ iii. $$-OSO_4Me$$ iv. $$-OSO_2CF_3$$
Weaker the base, better is the leaving group
The decreasing order of acidity is $$F_3C - SO_3H > MeSO_3H > AcOH > MeOH$$
The increasing order of basicity is $$F_3C^{\circleddash} < MeSO_3^{\circleddash} < AcO^{\circleddash} < MeO^{\circleddash}$$
$$(iv)$$ $$(iii)$$ $$(i)$$ $$(ii)$$
The decreaing order of leaving group ability is $$(iv) > (iii) > (i) > (ii)$$
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?
Among the following, the least stable resonance structure is :
Which of the following have +M effect ($$\bar { e }$$-donating mesomeric effect) ?
Which one of the following groups can exert both $$+ M$$ and $$- I$$ effect?