Delocalized Energy Is the Additional Stability Delocalized Electrons Give to a Compound

 Resonance is a mental exercise and method within the Valence Bond Theory of bonding that describes the delocalization of electrons within molecules. It compares and contrasts two or more possible Lewis structures that can represent a particular molecule. Resonance structures are used when one Lewis structure for a single molecule cannot fully describe the bonding that takes place between neighboring atoms relative to the empirical data for the actual bond lengths between those atoms. The net sum of valid resonance structures is defined as a resonance hybrid, which represents the overall delocalization of electrons within the molecule. A molecule that has several resonance structures is more stable than one with fewer. Some resonance structures are more favorable than others.


Electrons have no fixed position in atoms, compounds and molecules (see image below) but have probabilities of being found in certain spaces (orbitals). Resonance forms illustrate areas of higher probabilities (electron densities). This is like holding your hat in either your right hand or your left. The term Resonance is applied when  there are two or more possibilities available. Resonance structures do not change the relative positions of the atoms like your arms in the metaphor. The skeleton of the Lewis Structure remains the same, only the electron locations change.


Most arrows in chemistry cannot be used interchangeably and care must be given to selecting the correct arrow for the job.

  • ↔↔: A double headed arrow on both ends of the arrow between Lewis structures is used to show their inter-connectivity
  • ⇌⇌: Double harpoons are used to designate equilibria
  • ⇀⇀: A single harpoon on one end indicate the movement of one electron
  • →→: A double headed arrow on one end is used to indicate the movement of two electrons

Example 1: Ozone

 Consider ozone (O3)


ozone.jpg        Ozone-animation.gif

An animation of how one can do a resonance with ozone by moving electrons

Delocalization and Resonance Structures Rules

In resonance structures, the electrons are able to move to help stabilize the molecule. This movement of the electrons is called delocalization.

    1. Resonance structures should have the same number of electrons, do not add or subtract any electrons. (check the number of electrons by simply counting them).
    2. All resonance structures must follow the rules of writing Lewis Structures.
    3. The hybridization of the structure must stay the same.
    4. The skeleton of the structure can not be changed (only the electrons move).
    5. Resonance structures must also have the same amount of lone pairs.

Formal Charge

Even though the structures look the same, the formal charge (FC) may not be. Formal charges are charges that are assigned to a specific atom in a molecule. If computed correctly, the overall formal charge of the molecule should be the same as the oxidation charge of the molecule (the charge when you write out the empirical and molecular formula). We want to choose the resonance structure with the least formal charges that add up to zero or the charge of the overall molecule. The equation for finding Formal Charge is:

Formal Charge = (number of valence electrons in free orbital) – (number of lone-pair electrons) – ( [latex] \frac{1}{2} [/latex] number bond pair electrons)

The formal charge has to equal the molecule’s overall charge,e.g., the [latex] CNS^- [/latex] has an overall charge of -1, so the Lewis structure’s formal charge has to equal -1.

Example 2: Thiocyanate Ion

Consider the thiocyanate ([latex] CNS^- [/latex]) ion.


1. Find the Lewis Structure of the molecule. (Remember the Lewis Structure rules.)

CNS lewis structure.jpg

2. Resonance: All elements want an octet, and we can do that in multiple ways by moving the terminal atom’s electrons around (bonds too).

CNS resonance.jpg

3. Assign Formal Charges

Formal Charge = (number of valence electrons in free orbital) – (number of lone-pair electrons) – ( [latex] \frac{1}{2} [/latex] number bond pair electrons)

Remember to determine the number of valence electron each atom has before assigning Formal Charges

C = 4 valence e, N = 5 valence e, S = 6 valence e, also add an extra electron for the (-1) charge. The total of valence electrons is 16.

CNS FC.jpg

4. Find the most ideal resonance structure. (Note: It is the one with the least formal charges that adds up to zero or to the molecule’s overall charge.)

CNS FC1.jpg  CSN fc 2.jpg

5. Now we have to look at electronegativity for the “Correct” Lewis structure.

The most electronegative atom usually has the negative formal charge, while the least electronegative atom usually has the positive formal charges.

CNS best.jpg

Resonance Hybrids

Resonance Structures are a representation of a Resonance Hybrid, which is the combination of all resonance structures. The resonance structure with the Formal Charge closest to zero is the most accepted structure, however, the correct Lewis structure is actually a combination of all the resonance structures and is not solely describe as one.

    1. Draw the Lewis Structure & Resonance for the molecule (using solid lines for bonds).
    2. Where there can be a double or triple bond, draw a dotted line (—–) for a bond.
    3. Draw only the lone pairs found in all resonance structures, do not include the lone pairs that are not on all of the resonance structures.

Note: The correct Lewis structure is actually a combination of all the resonance structures and hence is not solely described as one.

Example 3: Carbonate Ion

Consider the carbonate ion: CO32



Step 1: Draw the Lewis Structure & Resonance.


Step 2: Combine the resonance structures by adding (dotted) bonds where other resonance bonds can be formed.


Step 3: Add only the lone pairs found on ALL resonance structures.


The bottom is the finished resonance hybrid for CO32-.

Rules for estimating stability of resonance structures

    1. The greater the number of covalent bonds, the greater the stability since more atoms will have complete octets
    2. The structure with the least number of formal charges is more stable
    3. The structure with the least separation of formal charge is more stable
    4. A structure with a negative charge on the more electronegative atom will be more stable
    5. Positive charges on the least electronegative atom (most electropositive) is more stable
    6. Resonance forms that are equivalent have no difference in stability and contribute equally (eg. benzene)

Example 4: Benzene and Aminophenol

Benzene is an extremely stable molecule and it is accounted for its geometry and molecular orbital interaction, but most importantly it’s due to its resonance structures. The delocalized electrons in the benzene ring make the molecule very stable and with its characteristics of a nucleophile, it will react with a strong electrophile only and after the first reactivity, the substituted benzene will depend on its resonance to direct the next position for the reaction to add a second substituent.

Aminophenol is a very stable molecule that is present in most biological systems, mainly in proteins. By studies of NMR spectroscopy and X-Ray crystallography it is confirmed that the stability of the amide is due to resonance which through molecular orbital interaction creates almost a double bond between the Nitrogen and the carbon.

Example 5: Multiple Resonance of other Molecules

Molecules with multiple resonance forms

Some structural resonance conformations are the major contributor or the dominant forms that the molecule exists. For example, if we look at the above rules for estimating the stability of a molecule, we see that for the third molecule the first and second forms are the major contributors for the overall stability of the molecule. The nitrogen is more electronegative than carbon so, it can handle the negative charge more than carbon. A carbon with a negative charge is the least favorable conformation for the molecule to exist, so the last resonance form contributes very little for the stability of the Ion.

The Hybrid Resonance forms show the different Lewis structures with the electron been delocalized. This is very important for the reactivity of chlorobenzene because in the presence of an electrophile it will react and the formation of another bond will be directed and determine by resonance. The long pair of electrons delocalized in the aromatic substituted ring is where it can potentially form a new bond with an electrophile, as it is shown there are three possible places that reactivity can take place, the first to react will take place at the para position with respect to the chloro substituent and then to either ortho position.


    1. Petrucci, Ralph H., et al. General Chemistry: Principles and Modern Applications. New Jersey: Pearson Prentice Hall, 2007.
    2. Ahmad, Wan-Yaacob and Zakaria, Mat B. “Drawing Lewis Structures from Lewis Symbols: A Direct Electron Pairing Approach.” Journal of Chemical Education: Journal 77.3.


    1. True or False, The picture below is a resonance structure?
    1. Draw the Lewis Dot Structure for SO42 and all possible resonance structures. Which of the following resonance structure is not favored among the Lewis Structures? Explain why. Assign Formal Charges.
    2. Draw the Lewis Dot Structure for CH3COO and all possible resonance structures. Assign Formal Charges. Choose the most favorable Lewis Structure.
    3. Draw the Lewis Dot Structure for HPO32 and all possible resonance structures. Assign Formal Charges.
    4. Draw the Lewis Dot Structure for CHO21 and all possible resonance structures. Assign Formal Charges.
    5. Draw the Resonance Hybrid Structure for PO43.
    6. Draw the Resonance Hybrid Structure for NO3.

Problems #2




Problems #2


    • Sharon Wei (UCD), Liza Chu (UCD)