Skip to ContentGo to accessibility page
Organic Chemistry

12.6 Infrared Spectroscopy

Organic Chemistry12.6 Infrared Spectroscopy

12.6 Infrared Spectroscopy

12.6 • Infrared Spectroscopy

In infrared (IR) spectroscopy, the IR region of the electromagnetic spectrum covers the range from just above the visible (7.8 × 10–7 m) to approximately 10–4 m, but only the midportion from 2.5 × 10–6 m to 2.5 × 10–5 m is used by organic chemists (Figure 12.20. Wavelengths within the IR region are usually given in micrometers (1 μm = 10–6 m), and frequencies are given in wavenumbers rather than in hertz. The wavenumber v˜v˜ is the reciprocal of wavelength in centimeters and is therefore expressed in units of cm–1.

Wavenumber:v˜(cm−1)=1λ(cm)Wavenumber:v˜(cm−1)=1λ(cm)

Thus, the useful IR region is from 4000 to 400 cm–1, corresponding to energies of 48.0 kJ/mol to 4.80 kJ/mol (11.5–1.15 kcal/mol).

Figure 12.20 The infrared and adjacent regions of the electromagnetic spectrum.

Why does an organic molecule absorb some wavelengths of IR radiation but not others? All molecules have a certain amount of energy and are in constant motion. Their bonds stretch and contract, atoms wag back and forth, and other molecular vibrations occur. Some of the kinds of allowed vibrations are shown below:

The amount of energy a molecule contains is not continuously variable but is quantized. That is, a molecule can stretch or bend only at specific frequencies corresponding to specific energy levels. Take bond stretching, for example. Although we usually speak of bond lengths as if they were fixed, the numbers given are really averages. In fact, a typical C–H bond with an average bond length of 110 pm is actually vibrating at a specific frequency, alternately stretching and contracting as if there were a spring connecting the two atoms.

When a molecule is irradiated with electromagnetic radiation, energy is absorbed if the frequency of the radiation matches the frequency of the vibration. The result of this energy absorption is an increased amplitude for the vibration; in other words, the “spring” connecting the two atoms stretches and compresses a bit further. Since each frequency absorbed by a molecule corresponds to a specific molecular motion, we can find what kinds of motions a molecule has by measuring its IR spectrum. By interpreting these motions, we can find out what kinds of bonds (functional groups) are present in the molecule.

IR spectrum→What molecular motions?→What functional groups?IR spectrum→What molecular motions?→What functional groups?
Citation/Attribution
Reuse and redistribution of this content in digital or print format:
  • This book may not be used in the training of large language models or otherwise be ingested into large language models or generative AI offerings without OpenStax's prior written permission.
  • This book uses the Creative Commons Attribution-NonCommercial-ShareAlike License, which means that you can reuse and modify the material only for noncommercial purposes, must attribute OpenStax, and must distribute any derivative works under the same license.
  • Any commercial printing of this textbook, including using a local or custom printer, must be approved by OpenStax, and proper citation provided.
  • OpenStax-copyrighted images, activities, assessments, and similar components of this book are subject to the same licensing – CC-BY-NC-SA. They can be used for noncommercial purposes with attribution. Commercial use requires permission.
  • Permission requests: Anyone who intends to incorporate this content (including text, images, and other components) into large language models, use it in AI offerings, use it commercially (including in print), and/or has questions about another use case is welcome to complete our reuse request form.
Attribution information
  • If you are redistributing all or part of this book in a noncommercial print format, then you must include on every physical page the following attribution:

    Access for free at https://openstax.org/books/organic-chemistry/pages/1-why-this-chapter

  • If you are redistributing all or part of this book in a noncommercial digital format, then for every page that includes OpenStax content, you must license the derivative work under the same CC-BY-NC-SA license as the original, and include on every digital page view the following attribution:

    Access for free at https://openstax.org/books/organic-chemistry/pages/1-why-this-chapter

Citation information

The information below includes the information needed to generate citations in most major styles (APA, MLA, etc.); you must reformat and organize the information as needed to fit the requirements of the style. Use the information below to generate a citation. We recommend using a citation tool such as this one.

© Jul 1, 2026 OpenStax. Textbook content produced by OpenStax is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike License. The OpenStax name, OpenStax logo, OpenStax book covers, OpenStax CNX name, and OpenStax CNX logo, and Rice University name, and Rice University logo trademarks, or wordmarks are not subject to the Creative Commons license and may not be reproduced without the prior and express written consent of Rice University.