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T: 2.6 R & F C: Opic Esonance Ormal Harge

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2.

TOPIC: 2.6 RESONANCE & FORMAL CHARGE


ENDURING UNDERSTANDING:
SAP-4 Molecular compounds are arranged based on Lewis diagrams and Valence Shell Electron Pair Repulsion
(VSEPR) theory.
LEARNING OBJECTIVE:
SAP-4.B Represent a molecule with a Lewis diagram that accounts for resonance between equivalent structures or that
uses formal charge to select between nonequivalent structures.
ESSENTIAL KNOWLEDGE:
SPQ-1.A.1 In cases where more than one equivalent Lewis structure can be constructed, resonance must be included as a
refinement to the Lewis structure. In many such cases, this refinement is needed to provide qualitatively
accurate predictions of molecular structure and properties.
SAP-4.B.2 The octet rule and formal charge can be used as criteria for determining which of several possible valid Lewis
diagrams provides the best model for predicting molecular structure and properties.
SAP-4.B.3 As with any model, there are limitations to the use of the Lewis structure model, particularly in cases with an
odd number of valence electrons
EQUATION(S):
Formal Charge = (# Valence Electrons) - (# lone electrons +# bonds connected)
(NOT ON EQN SHEET)

NOTES:

FORMAL CHARGE
When drawing Lewis Dot diagrams for some molecules and polyatomic ions, there can be several structures
drawn. Formal Charge is a method that can help determine which structure is most valid.

TO CALCULATE THE FORMAL CHARGE FOR EACH ATOM IN THE MOLECULE :


1. Determine the number of valence electrons of the atom.
2. Subtract the sum of the lone electrons and bonds connected to the atom from the valence electrons.

TO CHECK YOUR FORMAL CHARGE CALCULATION :


o The sum of the formal charges of each atom should add up to zero for a molecule or add up to the charge
for a polyatomic ion.

The most valid structure will have:


o Formal Charges as close to zero for all atoms. (Most preferable is “no formal charge.”)
o Negative Formal Charges will be placed on the most electronegative atom.

RESONANCE STRUCTURES
Sometimes when drawing a Lewis Structure you might find that there is more than one arrangement of
bond/electrons that are equally valid; you might find that a double (or triple) bond could be placed in one of two or
more places in a molecule or ion.
Look at the NO21- ion shown; both images are valid so both must be included when drawing a Lewis structure.

1 TOPIC: 2.6 Formal Charge & Resonance by Emily Miller is licensed under CC BY-NC-SA 4.0. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/4.0/
2.6
Resonance is structures are present simultaneously; they do not flip between them. The electrons can be
described as delocalized. The actual structure is an average of the resonance structures. As result, the bond lengths
are an average of the bonds present. In the NO21- ion the bond length is close to the average between a single and
double bond, a 1.5 bond.

To Represent Resonance: Draw all the structures of the molecule, keeping the arrangement of the atoms the same
but changing the location of the electrons. Double arrows are drawn between the structures indicating that the
structures are superimposed to make a hybrid.

I DO:
Calculate the formal charges for each atom in the molecule in hydrogen cyanide, HCN.

H-C ≡ N:
H = 1 – (0 + 1) = 0 C = 4 – (0 + 4) = 0 N = 5 – (3 + 2) = 0
Draw the resonance structures of the carbonate ion, CO32-.

WE DO:
Calculate the formal charge of each atom in the sulfate ion, SO42-.

Draw all resonance structures of SO2.

2 TOPIC: 2.6 Formal Charge & Resonance by Emily Miller is licensed under CC BY-NC-SA 4.0. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/4.0/
2.6
YOU DO:
1) Draw all resonance structures for Ozone, O3

2) Calculate the formal charge of each element in :

3) Draw all the possible resonance structures for the polyatomic ion ClO31-. Calculate the formal charge of
chlorine.

4) Knowing that benzene, C6H6, contains a ring, a student proposed the


following structure for benzene,
a) Calculate the formal charge for:
i. C

ii. C

iii. H

b) This structure is not the best description of the benzene


molecule. Explain why, citing formal charges.

c) Propose a better structure for benzene, include resonance structures if appropriate.

https://chem.libretexts.org/@api/deki/files/147339/8.6.2.png?revision=1&size=bestfit&width=249&heig
ht=150

3 TOPIC: 2.6 Formal Charge & Resonance by Emily Miller is licensed under CC BY-NC-SA 4.0. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/4.0/

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