Does the cyanide ion only have one dominant resonance structure? Why?

Answer 1

Yes, you could say that the cyanide ion has only one dominant resonance structure, and here's why you could do that.

You can draw two possible Lewis structures for the cyanide ion, #"CN"^(-)#, keeping in mind that you have 10 valence electrons to work with - 4 from carbon, 5 from nitrogen, and the extra electron that gives the anion its negative charge. Here's how those two structures would look

The structure on the left has a triple bond between the two atoms and a lone pair on each atom. The formal charges are zero for nitrogen, since it needs 5 electrons and it gets 5 electrons - 2 from the lone pair and 3 from the three bonds - and (-1) for carbon because it needs 4 electrons and gets 5 - 2 from the lone pair and 1 from each of the three bonds.

The second resonance structure you can draw will have a double bond between the atoms, one lone pair on carbon, and two lone pairs on nitrogen. This time, the (-1) formal charge is on nitrogen, since it now gets 6 electrons - 4 from the lone pairs and 2 from the bonds.

The major resonance contributor will be the first Lewis structure, despite the fact that it has the negative charge placed on the less electronegative atom - carbon. This happens because of the triple bond present, which acts as a powerful stabilizing factor.

The more stable resonance structures have the maximum number of covalent bonds, provided that all atoms have full octets.

Therefore, the major contributor to the hybrid structure shown above is the Lewis structure that has more covalent bonds.

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Answer 2

Yes, the cyanide ion (CN-) has one dominant resonance structure. This is because the carbon atom in CN- forms a triple bond with the nitrogen atom, and the nitrogen atom carries a lone pair of electrons. The other resonance structure, where the triple bond shifts to the nitrogen atom and forms a lone pair on the carbon atom, is less stable due to the electronegativity difference between carbon and nitrogen, making the triple bond more favorable on the carbon atom.

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Answer from HIX Tutor

When evaluating a one-sided limit, you need to be careful when a quantity is approaching zero since its sign is different depending on which way it is approaching zero from. Let us look at some examples.

When evaluating a one-sided limit, you need to be careful when a quantity is approaching zero since its sign is different depending on which way it is approaching zero from. Let us look at some examples.

When evaluating a one-sided limit, you need to be careful when a quantity is approaching zero since its sign is different depending on which way it is approaching zero from. Let us look at some examples.

When evaluating a one-sided limit, you need to be careful when a quantity is approaching zero since its sign is different depending on which way it is approaching zero from. Let us look at some examples.

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