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.
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 / group
Representative range
Typical appearance
What it suggests
O–H in an alcohol
3200–3550 cm⁻¹
Broad, strong
Alcohol or phenol; confirm with other evidence
O–H in a carboxylic acid
2500–3300 cm⁻¹
Very broad
Carboxylic acid, especially when C=O is also present
C=O
about 1680–1750 cm⁻¹
Strong, sharp
A carbonyl-containing family such as aldehyde, ketone, acid, ester or amide
C–H, sp³ carbon
about 2850–3000 cm⁻¹
Several medium peaks
Alkyl C–H bonds
C–O
about 1000–1300 cm⁻¹
Often strong, but inside the fingerprint region
May 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 amine
about 3300–3500 cm⁻¹
Often two relatively sharp N–H stretching bands
Primary amine; combine with other evidence
Common errors
Calling every broad peak O–H without checking its wavenumber.
Using one C=O band to decide immediately between an aldehyde, ketone, ester and acid.
Reading the x-axis in the wrong direction.
Treating the absence of a weak peak as absolute proof. Real spectra can be noisy or overlap.
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.