---
title: "Butadiene and an enone Template – Chemistry Diagram | MolDraw"
url: https://www.moldraw.com/templates/resonance-conjugated/
description: "Butadiene and an enone template: Buta-1,3-diene and but-3-en-2-one: the neutral form and the minor charge-separated form; for the enone the β-carbon carries…"
lang: en
publisher: Scidart Academy
generated: 2026-10-28
---
[MolDraw](https://www.moldraw.com/) › [Templates](https://www.moldraw.com/templates/) › [Resonance](https://www.moldraw.com/templates/resonance/) › Butadiene and an enone

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# Butadiene and an enone template

![Butadiene and an enone template: Buta-1,3-diene and but-3-en-2-one: the neutral form and the minor charge-separated form; for the enone the β-carbon carries δ+, as in conjugate addition.](https://www.moldraw.com/templates/resonance-conjugated.webp)

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Buta-1,3-diene and but-3-en-2-one: the neutral form and the minor charge-separated form; for the enone the β-carbon carries δ+, as in conjugate addition.

## What the template shows

- Charge-separated forms show where a conjugated π system is electron-poor
- Resonance contributors
- Buta-1,3-diene
- Neutral (major) ↔ charge-separated (minor)
- But-3-en-2-one
- The β-carbon becomes electrophilic
- Charge-separated forms are minor contributors, but they show the polarisation of the π system.
- Butadiene: the central C2–C3 bond (148 pm) is a little shorter than a normal C–C single bond, and the s-cis/s-trans rotation has a small barrier.
- Enone: the β-carbon is δ+, which is why nucleophiles add there (Michael and conjugate additions).
- Charges placed to match electronegativity (O⁻, C⁺) make a better minor form than the reverse.
- Contributors are not in equilibrium: the real species is one hybrid of them · every part of this figure is editable

Drawn with 18 atoms, 6 arrows, 3 shapes – every one editable in MolDraw.

## Sources

- [Clayden, Greeves & Warren, Organic Chemistry, 2nd ed., OUP 2012, ch. 7](https://openlibrary.org/isbn/9780199270293) Textbook
- [Smith, March's Advanced Organic Chemistry, 8th ed., Wiley 2020](https://openlibrary.org/isbn/9781119371809) Textbook

## How to use this template

1. Press **Edit in MolDraw**. The template opens on the canvas of the free MolDraw editor.
2. Change anything: move structures, edit atoms and labels, recolour highlights or delete what you do not need.
3. Add your own structures, arrows and text next to it, or combine several templates on one page.
4. Export the drawing as PNG, SVG or PDF for slides, worksheets, theses and papers.

## Frequently asked questions

### Is the Butadiene and an enone template free?

You can preview the Butadiene and an enone template here and open and edit it in MolDraw for free. Downloading or exporting it is part of MolDraw Pro, together with the other premium templates.

### Can I edit the Butadiene and an enone template?

Yes. It opens as an ordinary MolDraw drawing, so every structure, arrow, label and colour can be changed, and you can add your own content around it.

### Is the chemistry checked?

Every structure is checked with RDKit and every curly arrow passes MolDraw’s electron-flow audit. The sources used are listed on this page.

### How are resonance structures shown?

Each contributor is drawn separately, joined by double-headed resonance arrows, with curly arrows showing how the electrons move from one contributor to the next.

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