Separate resonance, formal charge and measured electron density
Preserve electron count and atom positions while changing a Lewis contributor.
Learning outcome: Compare all three double-bond sites for carbonate, then nitrate. Retain electron totals, every formal charge and the equal-contributor bond-order average.
Starting recap
Review the atomic electron ledger, signed energy changes and dimensional conversions. Distinguish a mathematical parameter from a unique material identification.
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Try
Carbonate has24 valence electrons; one double/two single contributor gives C formal0 and O formal0,−1,−1. Nitrate has the same electron total but central N formal+1.
Open the experimentPredict
Does moving the drawn double bond require the nuclei to switch positions or the molecule to oscillate between drawings?
Experiment
Compare all three double-bond sites for carbonate, then nitrate. Retain electron totals, every formal charge and the equal-contributor bond-order average.
Audit electron allocation across resonance contributors
Worked teaching model · synthetic values · Carbonate CO3²− and nitrate NO3− each have 24 valence electrons in the octet contributors shown: one double and two single central–O bonds, no central lone pair. Contributors differ only in electron allocation, not atom positions. Equal-contributor average is bookkeeping, not a molecule switching drawings.
Reset keeps your prediction, captures and practice history.
Axes rescale with settings. Compare numerical values, not screen slopes. Discrete stems show steps, contributors or partial sums; connected samples show the declared parameter relationship, not a measured time trajectory.
Numerical diagram coordinates
| oxygen site label | bond order in selected contributor |
|---|---|
| 1 | 2 |
| 2 | 1 |
| 3 | 1 |
Schematic connectivity only, not a scale drawing or measured electron density. Parentheses show formal charge; lone-pair counts complete the octet allocation.
| Site | Total attached bond order | Nonbonding electrons | Formal charge |
|---|---|---|---|
| central C | 4 | 0 | 0 |
| O1 | 2 | 4 | 0 |
| O2 | 1 | 6 | -1 |
| O3 | 1 | 6 | -1 |
Three oxygen labels identify unchanged atomic sites. Selecting another double-bond site changes a contributor, not the positions of nuclei or a timed molecular switch.
| Quantity | Value | Unit |
|---|---|---|
| Total valence electrons | 24 | electrons |
| Bonding electrons | 8 | electrons |
| Nonbonding electrons | 16 | electrons |
| Sum of formal charges | -2 | e |
| Equal-contributor central–O bond order | 1.333333 | ratio |
| Equal-contributor O formal allocation | -0.6666667 | e |
The electron total and net formal charge survive a change of contributor.
A single contributor has one formal double and two formal single bonds; three equivalent contributors distribute the representation over all O sites. Formal charge splits bond electrons equally and is not an experimentally unique partial charge. Nitrate central N carries +1 in these octet contributors, unlike carbonate central C.
Capture contrasting evidence and retain the interpretation limits. These supplied models do not identify an actual material or certify practical laboratory skill.
The electron total and net formal charge survive a change of contributor.
A single contributor has one formal double and two formal single bonds; three equivalent contributors distribute the representation over all O sites. Formal charge splits bond electrons equally and is not an experimentally unique partial charge. Nitrate central N carries +1 in these octet contributors, unlike carbonate central C.
Captures preserve recipes and replay their calculated results. They are synthetic model evidence, not physical measurements.
Understand
Apply
Public practice checks a specific claim. It does not establish independent mastery.
Distinguish formal charge, oxidation state, partial charge and the limits of an octet representation.
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