Organic Chemistry
Resonance in benzene is accompanied by delocalization of $$\pi$$ electrons. Each $$\pi$$ electron is attached with
Which of the following is correct with respect to the acidity of benzene sulphonic acid and benzoic acid?
The conjugate base of benzene sulphonic acid has greater resonance stabilization than benzoate ion, hence benzene sulphonic acid is a stronger acid than benzoic acid. $$PhSO^-_3$$ has three equivalent resonance structure, so more stable. but $$PhCOO^-$$ has only two equivalent resonance structure, so less stable.
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) ?