Identify characteristic functional-group IR absorptions

A fixed ethanoic-acid trace has a very broad 2500–3300 cm⁻¹ envelope and a strong 1712 cm⁻¹ band.

  • GCE A-Level H3 Chemistry 9813-2027
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Learning objectives

  • Identify characteristic functional-group IR absorptions

Read a spectrum as combined evidence

A fixed ethanoic-acid trace has a very broad 2500–3300 cm⁻¹ envelope and a strong 1712 cm⁻¹ band.

Together these support carboxylic-acid O–H and C=O; neither alone identifies the whole molecule.

Characteristic region and fingerprint

A characteristic absorption is a supplied range associated with a bond vibration, such as C=O near 1680–1750 cm⁻¹.

The fingerprint region contains many coupled vibrations and is used by comparison; it should not be treated as one functional-group label.

Use presence, absence, shape and intensity

Alcohol O–H is broad around 3200–3600 cm⁻¹; carboxylic-acid O–H is typically very broad around 2500–3300 cm⁻¹; C=O is strong near 1700 cm⁻¹.

A sharp band near 2250 cm⁻¹ may support C≡N, while absence of a broad O–H band can discriminate carbonyl candidates.

Distinguish acid from ester

Spectrum A: broad 2500–3300 plus strong 1712 cm⁻¹. Spectrum B: strong 1740 cm⁻¹ but no broad O–H.

A supports a carboxylic acid; B supports an ester or another non-O–H carbonyl and needs further evidence.

Try this

Classify the decisive functional groups in spectra A and B.

Check your answer

A strong answer should include acid O–H+C=O for A and carbonyl without O–H for B; do not claim a unique ester from one band.

Annotate a three-band trace

Mark 3350 cm⁻¹ broad, 1718 cm⁻¹ strong and 1050 cm⁻¹ strong on a hydroxy-carbonyl spectrum.

Use the supplied Data Booklet ranges and label uncertainty where bands overlap.

Try this

State which groups are supported by the three fixed bands.

Check your answer

Support O–H, C=O and C–O; a whole structure still requires formula or other evidence.

Use an important absence

A molecular formula C₃H₆O and a strong 1725 cm⁻¹ band support a carbonyl.

No aldehydic C–H features and no O–H narrow the candidates but do not replace full-spectrum reasoning.

Try this

Compare propanone and propanal using the supplied positive and negative evidence.

Check your answer

Propanone is better supported only if the aldehydic C–H evidence is absent; state the limitations of IR alone.

One peak is not one structure

Functional-group assignment is probabilistic evidence constrained by ranges, band shape and important absences.

Combine at least two independent features before naming a functional-group class where possible.

Try this

Better reasoning: “A 1715 cm⁻¹ band proves the sample is propanone.”

Check your answer

State only that a carbonyl is supported, then request formula and other bands before choosing propanone.

From bands to candidate structures

After the check questions, try the nitrile example without notes. Return later for a different amide question.

Try this next: deduce structures.

Try this

Annotate the fixed ethanoic-acid trace with range, shape and group.

Check your answer

A strong answer should include broad acid O–H at 2500–3300 and strong C=O near 1712 cm⁻¹, with a combined rather than single-peak conclusion.

Identify characteristic functional-group IR absorptions scientific representation

Two separate transmittance traces run from 4000 to 500 cm⁻¹. Ethanoic acid has a very broad trough from 2500 to 3300, a strong trough at 1712 and a band around 1260. Ethyl ethanoate has a weak band just below 3000, a strong trough at 1740 and a band around 1160, with no broad trough from 2500 to 3600.

About 5 minutes

Key visual: Identify characteristic functional-group IR absorptions. Two labelled transmittance traces support range, shape, intensity and absence reasoning for separate compounds.
Identify characteristic functional-group IR absorptions authored spectrumTwo separate transmittance traces run from 4000 to 500 cm⁻¹. Ethanoic acid has a very broad trough from 2500 to 3300, a strong trough at 1712 and a band around 1260. Ethyl ethanoate has a weak band just below 3000, a strong trough at 1740 and a band around 1160, with no broad trough from 2500 to 3600.transmittance / %wavenumber / cm⁻¹ (high → low)40005002500–3300 broad1712 strong1210–1320below 30001740 ester1050–1300Ethanoic acidEthyl ethanoate
Ordered functional-group band evidence
SampleWavenumber / cm⁻¹Strength / widthAssignmentExplicit absence
ethanoic acid2500–3300very broad, strongO–H—
ethanoic acid1712strongC=O—
ethanoic acid1210–1320strong clusterC–O—
ethyl ethanoate1740; 1050–1300strong; strong clusterC=O; C–Ono broad 2500–3600 O–H

Text alternative: Two separate transmittance traces run from 4000 to 500 cm⁻¹. Ethanoic acid has a very broad trough from 2500 to 3300, a strong trough at 1712 and a band around 1260. Ethyl ethanoate has a weak band just below 3000, a strong trough at 1740 and a band around 1160, with no broad trough from 2500 to 3600.