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// CHEMISTRY L5 — SPECTROSCOPY

Read a molecule's fingerprint.

Chemists identify an unknown compound without ever seeing it — by the way it breaks apart, absorbs infrared light, and lines up its hydrogens. Pick a molecule and compare its three spectra side by side.
// FIG. 01 — THE SPECTROMETER BENCH
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// THREE TECHNIQUES, THREE QUESTIONS
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// THE FINGERPRINT REGION
In an infrared spectrum, the region below about 1500 cm⁻¹ is called the fingerprint region. It's a dense, messy set of dips that is unique to each compound — like a barcode. You don't try to assign every peak; instead you match the whole pattern against a database. The bands above 1500 cm⁻¹ (O–H, N–H, C–H, C=O) are the ones you read directly to spot functional groups.
// REFERENCES & FURTHER READING
Wikipedia — Spectroscopy ↗ Wikipedia — Mass spectrometry ↗ Wikipedia — NMR spectroscopy ↗
Cross-check against your own exam board's specification (AQA, Edexcel, OCR, SQA).
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Lizard-Spock STEM Academy — learn by doingCHEMISTRY L5 / SPECTROSCOPY