Which of the following is the most unstable r | vedclass

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(C) The stability of resonance structures is determined by several factors: $1$. Structures with more covalent bonds are more stable. $2$. Structures

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(C) The stability of resonance structures is determined by several factors: $1$. Structures with more covalent bonds are more stable. $2$. Structures with complete octets for all atoms are more stable. $3$. Structures with negative charges on more electronegative atoms and positive charges on less electronegative atoms are more stable. $4$. Structures with like charges on adjacent atoms are highly unstable due to electrostatic repulsion. In the $p$-nitrophenoxide ion,the resonance involves the delocalization of the negative charge from the phenoxide oxygen into the nitro group. Structure $C$ shows a positive charge on the nitrogen atom and a negative charge on the oxygen atom,which is a standard resonance contributor. Structure $D$ shows a negative charge on a carbon atom adjacent to the ring,which is less stable than having it on oxygen. Structure $B$ is a valid resonance structure. Structure $A$ shows a negative charge on the phenoxide oxygen and a positive charge on the nitrogen,but it also implies a charge distribution that is less favorable compared to others. However,looking at the structures provided,structure $C$ is the most unstable because it places a positive charge on the nitrogen atom while having a negative charge on the oxygen atom in a way that disrupts the aromaticity and creates significant charge separation without the benefit of full octets or favorable electronegativity distribution compared to the others. Actually,structure $C$ is the most unstable because it has a positive charge on the nitrogen and a negative charge on the oxygen,but it lacks the necessary double bond character to stabilize the system effectively compared to the other resonance forms.

Which of the following is the most unstable resonance structure of the $p$-nitrophenoxide ion?

Similar Questions

The correct order of decreasing length of the bond as indicated by the arrow in the following structures is:

Correct statements for the given reaction are :
$A$. Compound '$B$' is aromatic
$B$. The completion of above reaction is very slow
$C$. '$A$' shows tautomerism
$D$. The bond lengths $C-C$ in compound $B$ are found to be same
Choose the correct answer from the options given below :

Which of the following stability order comparisons for resonating structures is incorrect?

Among the following,the antiaromatic compounds are:

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