Amphetamine Lewis Structure

Amphetamine Lewis Structure: C₉H₁₃N Lewis Structure, tetrahedral Geometry, sp3 Hybridization & Polarity

Amphetamine Key Facts

The Amphetamine Lewis structure is C–C single bond and 3 C–H single bond; the central C has 4 electron domains (0 lone pairs), giving a tetrahedral electron-domain arrangement and a tetrahedral molecular geometry with a 109.5° bond angle. C is best described as sp3-hybridized, and Amphetamine is polar because the tetrahedral shape (and/or unequal terminal atoms) prevents cancellation of the bond dipoles.

Figure 1: Lewis Structure of Amphetamine (C₉H₁₃N)

Chemical Formula	C₉H₁₃N
CAS Number	300-62-9
Total Valence Electrons	54
Lewis Structure	C–C single bond and 3 C–H single bond
Electron-Domain Geometry	tetrahedral
Molecular Geometry	tetrahedral
Hybridization Model	sp3 (central C)
Bond Angle	109.5°
Polarity	Polar molecule

PubChem (CID 3007) and NIST list Amphetamine as C ₉H ₁₃N with CAS 300-62-9; molecular weight ≈ 135.21 g/mol. View CAS 300-62-9 dictionary details on Guidechem →

Applications of Amphetamine (CAS 300-62-9)

Amines are intermediates for dyes, pharmaceuticals, agrochemicals, rubber chemicals and surfactants; they act as nucleophiles and bases in a vast range of N-containing syntheses.

Pharma & Agro Backbone of many active ingredients and crop-protection agents.

Dyes & Polymers Coupling components for dyes and epoxy curatives.

Intermediate Nucleophile/base in alkylation, acylation and amidation.

Procurement Note "Amphetamine" 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 300-62-9 as the primary identifier when screening suppliers; always confirm regional availability and safety documentation (SDS).

Step 1 - Valence Electrons & Central Atom

To draw the Amphetamine Lewis structure we first count the total valence electrons. C₉H₁₃N contains 9×4 (C) + 13×1 (H) + 5 (N); the net charge of 0 gives a total of 54 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 = 9×4 (C) + 13×1 (H) + 5 (N) = 54 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–C single bond and 3 C–H 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.

C–C C–H ×3

C: 0 lone pairs, 4 bonding domains

4 bonding domains + 0 lone pairs = 4 electron domains

Octet Rule: Why C Has Eight Electrons C forms 4 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 4 electron domains around C arrange to minimize mutual repulsion, giving an tetrahedral 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 tetrahedral; the C bond angle is set to 109.5° 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 sp3 hybrid orbitals to form the 4 equivalent electron-domain directions (4 bonding + 0 lone pair).

Formal-charge check

Formal charge on central C = V − N − ½B = 4 − 0 − ½×8 = 3. The nonzero formal charge is distributed by resonance / charge separation; the drawn structure is the lowest-energy contributor.

Modeling Note Modeling Note: sp3 is a compact model for the 4 electron-domain directions around C; full quantum-chemical treatments use molecular orbitals.

Is Amphetamine Polar or Nonpolar?

Amphetamine is polar. The tetrahedral shape prevents cancellation of the bond dipoles. The bond dipoles do not cancel, leaving a net molecular dipole, which strongly influences solvation behavior and intermolecular interactions.

Expert Quote — Structural Chemistry Perspective

The decisive structural fact is not simply that the individual bonds are polar; it is whether molecular symmetry allows their vector sum to vanish. In Amphetamine the tetrahedral arrangement prevents cancellation, so a permanent dipole remains.

Interpretation consistent with standard VSEPR / molecular-geometry references.

This polarity profile underpins its behavior as a solvent, reactant or process intermediate; when sourcing, specify grade and container compatibility.

Structural Comparison Table

Species	Formula	Central Atom	Electron Domains	Molecular Geometry	Polarity
Amphetamine	C₉H₁₃N	C	4	tetrahedral	Polar
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 54 valence electrons of C₉H₁₃N, draw the Lewis structure and confirm the central C atom is sp3-hybridized with tetrahedral 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 Amphetamine (CAS 300-62-9)? Browse Supplier on Guidechem →

FAQs

Is C₉H₁₃N polar or nonpolar?

Amphetamine is polar. Its tetrahedral geometry (and/or unequal terminal atoms) stops the bond dipoles from cancelling.

What is the Lewis structure of Amphetamine?

C–C single bond and 3 C–H single bond; no lone pairs on C. It uses all 54 valence electrons and the preferred structure carries a formal charge of 3 on the central atom.

What is the bond angle in Amphetamine?

The C angle is about 109.5°. Lone-pair repulsion compresses the angle from the ideal tetrahedral value.

What is the hybridization of C in Amphetamine?

The conventional model is sp3. Amphetamine has 4 electron domains around the central C.

What is the CAS number of Amphetamine?

The CAS number is 300-62-9. PubChem (CID 3007) and NIST identify this with C₉H₁₃N; use it to locate suppliers and database records.

References

PubChem CID 3007, Amphetamine. Molecular formula, CAS number, molecular weight and chemical identity.
NIST Chemistry WebBook, SRD 69, Amphetamine. Formula, CAS Registry Number and thermochemical / spectroscopic data.
IUPAC Gold Book. Definitions for "lone pair", "VSEPR", "hybridization" and "formal charge".
Atkins, P. & de Paula, J., Physical Chemistry. VSEPR, molecular geometry and dipole moments.
Guidechem supplier & dictionary records. Commercial sourcing and CAS-linked property pages for Amphetamine (CAS 300-62-9).

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 300-62-9 identifies the substance, not a universal purity specification.

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Amphetamine Lewis Structure

Amphetamine Lewis Structure