Frequency to Wavenumber Converter
Common Conversions
| Hz | cm⁻¹ |
|---|---|
| 29980000000 | 1 |
| 299800000000 | 10 |
| 2998000000000 | 100 |
| 14990000000000 | 500 |
| 29980000000000 | 1000 |
| 59960000000000 | 2000 |
| 89940000000000 | 3000 |
| 119900000000000 | 4000 |
| 149900000000000 | 5000 |
| 299800000000000 | 10000 |
| 599600000000000 | 20000 |
| 1499000000000000 | 50000 |
Why this conversion matters in chemistry
Frequency and wavenumber describe the same light, but spectroscopy strongly prefers wavenumber because it's proportional to photon energy. Raw frequency in hertz is what shows up in time-domain measurements, FTIR software outputs, or theoretical calculations — but by the time the result lands in a paper, it's in cm⁻¹. Divide the frequency in Hz by 2.998 × 10¹⁰ cm/s and you have your wavenumber. A C=O stretch at 5.1 × 10¹³ Hz becomes 1700 cm⁻¹, which is the number every organic chemistry textbook quotes. After enough spectra you stop thinking of them as two different scales; you just read one off the other.
Formula
Worked Examples
Mid-IR, right in the fingerprint region. About 30 THz — a clean anchor worth remembering for spectral bookkeeping.
The C–H stretching region. Any aliphatic spectrum has peaks clustered around here.
A generic carbonyl C=O stretch. Exact position shifts with context — aldehydes sit near 1725 cm⁻¹, ketones 1715, esters 1735, amides 1650–1680 — and that sensitivity is exactly what makes the band so diagnostic.
Far-IR, or what physics labs call the terahertz range. Low-energy lattice vibrations and some metal-ligand stretches live out here.