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When infrared (IR) radiation passes through a molecule, the bonds stretch or bend by absorbing the radiation. This absorption creates the molecule's absorption spectrum, which is the plot of its percentage transmittance versus wavenumber.

Transmittance is defined as the ratio of the radiant power passing through a sample to that from the radiation's source. Multiplying the transmittance by 100 gives the percent transmittance (%T), which varies between 100% (no absorption) and 0% (complete absorption). When IR radiation passes through a molecule, 100% transmittance indicates that the molecule has not absorbed any energy. Conversely, lower percentage transmittance values suggest that the molecule has absorbed some energy, allowing us to obtain the IR spectrum. Each downward-pointing peak in the spectrum is called an absorption band. Usually, the position of the absorption band in the IR spectrum is reported using wavenumber or frequency values. In the IR spectrum, wavenumber values range from 400 to 4000 cm−1.

In the IR spectrum, signals on the left side correspond to higher-energy and higher-frequency radiations, whereas those on the right side denote low-energy, low-frequency radiations. Based on shape and intensity, these signals are categorized as strong, medium, weak, broad, or sharp.

The IR spectrum can be divided into two main regions. The functional group region or diagnostic region is the left two-thirds portion of the spectrum. The absorption bands corresponding to most functional groups can be observed in this area. The right-hand side of the spectrum is referred to as the fingerprint region. Similar to the fingerprint of individuals, this region is unique to each compound. The diagnostic region of an infrared spectrum is dominated by bond stretching vibrations, while the fingerprint region is characterized by more complex vibrations like bond rocking, bending, and twisting. Although two compounds may contain the same functional group, they will show a unique pattern in the fingerprint region due to the differences in their chemical environment.

From Chapter 13:

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13.5 : IR Spectrum

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13.1 : Infrared (IR) Spectroscopy: Overview

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13.2 : IR Spectroscopy: Molecular Vibration Overview

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13.3 : IR Spectroscopy: Hooke's Law Approximation of Molecular Vibration

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13.4 : IR Spectrometers

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13.6 : IR Absorption Frequency: Hybridization

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13.7 : IR Absorption Frequency: Delocalization

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13.8 : IR Frequency Region: X–H Stretching

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13.9 : IR Frequency Region: Alkyne and Nitrile Stretching

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13.10 : IR Frequency Region: Alkene and Carbonyl Stretching

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13.11 : IR Frequency Region: Fingerprint Region

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13.12 : IR Spectrum Peak Intensity: Amount of IR-Active Bonds

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13.13 : IR Spectrum Peak Intensity: Dipole Moment

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13.14 : IR Spectrum Peak Broadening: Hydrogen Bonding

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13.15 : IR Spectrum Peak Splitting: Symmetric vs Asymmetric Vibrations

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