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Carbonic acid Lewis Structure

Carbonic acid Lewis structure (CH2O3). C–O double bond, C–O single bond and C–O single bond. It shows a trigonal planar shape, sp2 hybridization on C, 120° bond angles. Count 24 valence electrons and a trigonal planar electron-domain arrangement. Jackson3 MIN READSeptember 30, 2026

Carbonic acid Lewis Structure: CH2O3 Lewis Structure, trigonal planar Geometry, sp2 Hybridization & Polarity

Carbonic acid Lewis structure Cover

Carbonic acid Key Facts

The Carbonic acid Lewis structure is C–O double bond, C–O single bond and C–O single bond; the central C has 3 electron domains (0 lone pairs), giving a trigonal planar electron-domain arrangement and a trigonal planar molecular geometry with a 120° bond angle. C is best described as sp2-hybridized, and Carbonic acid is nonpolar because the bond dipoles cancel by molecular symmetry.

Carbonic acid Lewis Structure Figure 1: Lewis Structure of Carbonic acid (CH2O3)
Chemical Formula CH2O3
CAS Number 463-79-6
Total Valence Electrons 24
Lewis Structure C–O double bond, C–O single bond and C–O single bond
Electron-Domain Geometry trigonal planar
Molecular Geometry trigonal planar
Hybridization Model sp2 (central C)
Bond Angle 120°
Polarity Nonpolar molecule
PubChem (CID 767) and NIST list Carbonic acid as CH 2O 3 with CAS 463-79-6; molecular weight ≈ 62.025 g/mol. View CAS 463-79-6 dictionary details on Guidechem →

Applications of Carbonic acid (CAS 463-79-6)

Carboxylic acids and esters are flavors, fragrances, polymers (PET, polyesters, alkyds) and solvents/intermediates; acetate and phthalate esters are plasticizers, and acids are precursors to salts, amides and anhydrides.

Polymers & Resins PET, polyesters and alkyd coatings from acid/ester chemistry.
Solvents & Plasticizers Esters as solvents; phthalates/acetates as flexibilizers.
Flavor & Fine Chem Esters in flavors/fragrances and active-ingredient synthesis.
Procurement Note "Carbonic acid" is supplied in multiple commercial grades and package sizes. Specify purity, grade, moisture/impurity limits, package (cylinder, drum or bulk) and intended process, and use CAS 463-79-6 as the primary identifier when screening suppliers; always confirm regional availability and safety documentation (SDS).

Step 1 - Valence Electrons & Central Atom

To draw the Carbonic acid Lewis structure we first count the total valence electrons. CH2O3 contains 4 (C) + 2×1 (H) + 3×6 (O); the net charge of 0 gives a total of 24 valence electrons to place.

The central atom is C. It is the least electronegative atom capable of forming multiple bonds and is surrounded by the more electronegative terminal atom(s); hydrogen, when present, always occupies a terminal position. Electronegativity considerations place the electron density toward the terminal atom(s).

Valence-electron count

Total valence electrons = 4 (C) + 2×1 (H) + 3×6 (O) = 24 electrons.

Step 2 - Lewis Structure & Electron Distribution

Place C at the center and connect each surrounding atom with a single bond, complete octets on the terminal atoms, and place any remaining electrons on the central atom. The resulting electron distribution is: C–O double bond, C–O single bond and C–O single bond; no lone pairs on C.

Counting bonding and nonbonding electrons around C therefore satisfies the octet/expanded-octet requirement for the drawn structure.

This species is best represented by resonance structures; the π bonding is delocalized over the equivalent terminal atom(s), so all C–terminals bonds are equivalent in the resonance hybrid.

C=O C–O C–O
C: 0 lone pairs, 3 bonding domains
3 bonding domains + 0 lone pairs = 3 electron domains
Octet Rule: Why C Has Eight Electrons C forms 3 bond(s) and retains 0 nonbonding electron(s), reaching an octet. No expanded octet is required for this second-row (or octet-satisfying) central atom.

Step 3 - VSEPR Theory & Geometry

VSEPR theory states that the 3 electron domains around C arrange to minimize mutual repulsion, giving an trigonal planar electron-domain geometry.

Because 0 of these domains are lone pair(s) — and lone pairs repel more strongly than bonding pairs — the observed molecular geometry is trigonal planar; the C bond angle is set to 120° rather than the ideal value for the electron-domain geometry.

Repulsion hierarchy

A useful VSEPR approximation is: lone pair–lone pair repulsion > lone pair–bonding pair repulsion > bonding pair–bonding pair repulsion. With 0 lone pair(s) on C, the lone-pair domains occupy positions that minimize overall repulsion while pushing the bonding domains (and therefore the bonded atoms) closer together.

Hybridization & Formal Charge

In the conventional localized-bond model, C uses sp2 hybrid orbitals to form the 3 equivalent electron-domain directions (3 bonding + 0 lone pair).

Formal-charge check

Formal charge on central C = V − N − ½B = 4 − 0 − ½×8 = 0. The preferred Lewis structure carries zero formal charge on the central atom (and on the terminals), so it is the dominant contributor.

Modeling Note Modeling Note: sp2 is a compact model for the 3 electron-domain directions around C; full quantum-chemical treatments use molecular orbitals.

Is Carbonic acid Polar or Nonpolar?

Carbonic acid is nonpolar. Although individual C–terminal bonds are polar when the atoms differ in electronegativity, the trigonal planar geometry makes their vector sum zero, so there is no net molecular dipole.

Expert Quote — Structural Chemistry Perspective

A common misconception is that polar bonds guarantee a polar molecule. Carbonic acid shows the opposite: identical bond dipoles arranged with trigonal planar symmetry cancel exactly, yielding a nonpolar species.

Interpretation consistent with standard VSEPR / molecular-geometry references.

Its nonpolar character governs solvation and intermolecular behavior; specify grade and handling when sourcing.

Structural Comparison Table

Species Formula Central Atom Electron Domains Molecular Geometry Polarity
Carbonic acid CH2O3 C 3 trigonal planar Nonpolar
Carbon dioxide CO2 C 2 linear Nonpolar
Carbon monoxide CO C 2 linear (diatomic) Polar
Carbon disulfide CS2 C 2 linear Nonpolar
Methane CH4 C 4 tetrahedral Nonpolar
Ethane C2H6 C 4 tetrahedral Nonpolar
Practice question Starting from the 24 valence electrons of CH2O3, draw the Lewis structure and confirm the central C atom is sp2-hybridized with trigonal planar geometry. What happens to the bond angle if one terminal atom is replaced by a more electronegative substituent?
Looking for industrial bulk or specified-grade supplies of Carbonic acid (CAS 463-79-6)? Browse Supplier on Guidechem →

FAQs

Is CH2O3 polar or nonpolar?

Carbonic acid is nonpolar. Its trigonal planar symmetry cancels the bond dipoles exactly.

What is the Lewis structure of Carbonic acid?

C–O double bond, C–O single bond and C–O single bond; no lone pairs on C. It uses all 24 valence electrons and the preferred structure carries zero formal charge on the central atom.

What is the bond angle in Carbonic acid?

The C angle is about 120°. Lone-pair repulsion compresses the angle from the ideal trigonal planar value.

What is the hybridization of C in Carbonic acid?

The conventional model is sp2. Carbonic acid has 3 electron domains around the central C.

What is the CAS number of Carbonic acid?

The CAS number is 463-79-6. PubChem (CID 767) and NIST identify this with CH2O3; use it to locate suppliers and database records.

References

  1. PubChem CID 767, Carbonic acid. Molecular formula, CAS number, molecular weight and chemical identity.
  2. NIST Chemistry WebBook, SRD 69, Carbonic acid. Formula, CAS Registry Number and thermochemical / spectroscopic data.
  3. IUPAC Gold Book. Definitions for "lone pair", "VSEPR", "hybridization" and "formal charge".
  4. Atkins, P. & de Paula, J., Physical Chemistry. VSEPR, molecular geometry and dipole moments.
  5. Guidechem supplier & dictionary records. Commercial sourcing and CAS-linked property pages for Carbonic acid (CAS 463-79-6).

Technical scope: Lewis structures, VSEPR and hybridization are model-based descriptions for chemical communication and structure prediction; actual molecular electronic structure is more accurately represented by molecular-orbital and quantum-chemical methods. Commercial grades vary substantially by supplier and intended use; CAS 463-79-6 identifies the substance, not a universal purity specification.

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