Organic Chemistry
Resonance in benzene is accompanied by delocalization of $$\pi$$ electrons. Each $$\pi$$ electron is attached with
The correct order of stability for the given alkoxides is :
[Ref. image 1]
Here, in this case, we have to determine the stability of alkoxides.
Here $$C$$ is more stable because in this case -ve charge on $$O$$ is in conjugation with a double bond and $$NO_2$$. So there is an extra double bond in conjugation as,
[Ref. image 2]
Then comes $$B$$ as in case of $$B$$, -ve charge on oxygen is in conjugation with a double bond and not with $$NO_2$$
[Ref. image 3]
In case of $$A$$, there is no double bond so, no conjugation possible. So, least stable.
So, stability order is $$C > B > A$$
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 "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) ?
Which one of the following groups can exert both $$+ M$$ and $$- I$$ effect?