---
title: "Meso compounds: 2,3-dibromobutane Template | MolDraw"
url: https://www.moldraw.com/templates/stereo-meso-dibromobutane/
description: "Meso compounds: 2,3-dibromobutane template: 2,3-Dibromobutane in Fischer projection and wedge–dash: the (2R,3R)/(2S,3S) enantiomers and the achiral meso…"
lang: en
publisher: Scidart Academy
generated: 2026-10-28
---
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# Meso compounds: 2,3-dibromobutane template

![Meso compounds: 2,3-dibromobutane template: 2,3-Dibromobutane in Fischer projection and wedge–dash: the (2R,3R)/(2S,3S) enantiomers and the achiral meso (2R,3S) isomer with its mirror plane.](https://www.moldraw.com/templates/stereo-meso-dibromobutane.webp)

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2,3-Dibromobutane in Fischer projection and wedge–dash: the (2R,3R)/(2S,3S) enantiomers and the achiral meso (2R,3S) isomer with its mirror plane.

## What the template shows

- Two stereocentres but only three stereoisomers: the (2R,3S) form has a mirror plane
- The three stereoisomers
- chiral, the enantiomer
- mirror plane
- achiral: mirror plane between C2 and C3
- A meso compound has stereocentres but is achiral: an internal mirror plane maps one half onto the other, so it is superimposable on its mirror image.
- In meso compounds the centres carry opposite labels (2R,3S); (2R,3S) and (2S,3R) are the same compound.
- So 2,3-dibromobutane has three stereoisomers, not 2² = 4: one pair of enantiomers and the meso form, a diastereomer of both.
- The meso form is optically inactive by itself, unlike a racemate, which is a 1 : 1 mixture of two chiral compounds.
- Wedge = toward you, hash = away from you · every part of this figure is editable

Drawn with 18 atoms, 24 shapes – every one editable in MolDraw.

## Sources

- [Clayden, Greeves & Warren, Organic Chemistry, 2nd ed., OUP 2012, ch. 14](https://openlibrary.org/isbn/9780199270293) Textbook
- [Eliel & Wilen, Stereochemistry of Organic Compounds, Wiley 1994, ch. 3](https://openlibrary.org/isbn/9780471016700) Textbook
- [Moss, Basic terminology of stereochemistry (IUPAC Recommendations 1996), Pure Appl. Chem. 1996, 68, 2193](https://doi.org/10.1351/pac199668122193) IUPAC

## 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 Meso compounds: 2,3-dibromobutane template free?

You can preview the Meso compounds: 2,3-dibromobutane 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 Meso compounds: 2,3-dibromobutane 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.

### Are the R/S labels in the stereochemistry templates checked?

Yes. Every R/S and E/Z descriptor is computed with RDKit from the drawn structure, so the labels match the wedges and dashes.

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