Module 2

IR spectroscopy: bonds absorb and vibrate

Infrared radiation is absorbed when its frequency matches a molecular vibration that changes the molecule’s . Different bond types absorb in useful wavenumber ranges.

Instrumentation workflow

Connect each physical stage to the downward trough that appears in a transmittance spectrum.

1 IR sourceProvides a range of IR frequencies.
2 SampleA matching IR-active vibration absorbs energy.
3 DetectorMeasures how much radiation remains.
4 SpectrumLower transmittance becomes a downward band.
Core relationship: matching vibration absorbs IR → less radiation reaches the detector → transmittance falls at that wavenumber.

Scan an IR beam across a molecule

Spectrum being drawn

Move the slider. The marker sweeps across the wavenumber scale and the simplified transmittance spectrum is drawn as the instrument scans.

4000 cm⁻¹500 cm⁻¹
At 3350 cm⁻¹: the ethanol O–H bond absorbs strongly across a broad range and stretches.

Interactive spectrum: click a band to highlight the bond

Every model now shows all main bonds so you can see exactly which bond is being matched to the band.

Ethanol IR spectrum

Key absorptions

Select a band. The associated bond will animate in the structure.

Functional-group region

Above about 1500 cm⁻¹, several highly useful absorptions occur. Examples include broad O–H, strong C=O and C–H stretching bands.

Use ranges rather than expecting one exact number. Bond strength, neighbouring atoms, hydrogen bonding and sample conditions can shift a band.

Fingerprint region

The region below about 1500 cm⁻¹ contains many overlapping vibrations involving much of the molecule. It is shaded red in the interactive spectra because individual peaks in this region are usually less reliable for assigning one specific bond.

The overall jagged pattern can help confirm identity by comparison with a reference spectrum, but at VCE level use clearly diagnostic bands above 1500 cm⁻¹ first.

Textbook guide to common VCE absorptions

Bond / groupRepresentative rangeTypical appearanceWhat it suggests
O–H in an alcohol3200–3550 cm⁻¹Broad, strongAlcohol or phenol; confirm with other evidence
O–H in a carboxylic acid2500–3300 cm⁻¹Very broadCarboxylic acid, especially when C=O is also present
C=Oabout 1680–1750 cm⁻¹Strong, sharpA carbonyl-containing family such as aldehyde, ketone, acid, ester or amide
C–H, sp³ carbonabout 2850–3000 cm⁻¹Several medium peaksAlkyl C–H bonds
C–Oabout 1000–1300 cm⁻¹Often strong, but inside the fingerprint regionMay support a C–O bond, but is less reliable as an isolated assignment because it lies below 1500 cm⁻¹
N–H in a primary amineabout 3300–3500 cm⁻¹Often two relatively sharp N–H stretching bandsPrimary amine; combine with other evidence

Common errors

Question bank: 4 sets of 5

The bank is split into four mixed sets of five questions. Each set combines instrument and interpretation content. Answer choices are shuffled once when the attempt begins, then remain fixed while you work.