Experiment: Interpretation of UV–Visible Spectrum and Calculation of λmax of 1,3,5-Hexatriene
Aim
To record and interpret the UV–Visible spectrum of 1,3,5-hexatriene and determine its maximum absorption wavelength (λmax).
Principle
1,3,5-Hexatriene contains three conjugated double bonds. Conjugation allows π-electrons to become delocalized, lowering the energy required for electronic transitions.
When ultraviolet light is absorbed, electrons undergo π → π* transition. The absorption occurs at a specific wavelength where the absorbance becomes maximum, known as λmax.
As the number of conjugated double bonds increases, the absorption shifts to longer wavelength (bathochromic shift).
Absorbance follows Beer–Lambert Law:
Where
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A = Absorbance
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ε = Molar absorptivity
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c = Concentration
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l = Path length of cuvette
Apparatus
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UV–Visible spectrophotometer
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Quartz cuvette
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Volumetric flask
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Pipette
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Beaker
Chemicals / Reagents
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1,3,5-Hexatriene
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Ethanol or hexane (solvent)
Procedure
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Prepare a dilute solution of 1,3,5-hexatriene in hexane or ethanol.
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Fill a quartz cuvette with solvent and set it as the blank in the spectrophotometer.
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Fill another cuvette with the sample solution.
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Scan the spectrum in the range 200–350 nm.
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Record absorbance values at different wavelengths.
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Plot a graph of Absorbance vs Wavelength.
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Identify the wavelength corresponding to maximum absorbance (λmax).
Observation Table
| Sr. No. | Wavelength (nm) | Absorbance |
|---|---|---|
| 1 | 230 | 0.18 |
| 2 | 240 | 0.36 |
| 3 | 250 | 0.64 |
| 4 | 255 | 0.82 |
| 5 | 258 | 0.94 |
| 6 | 260 | 0.88 |
| 7 | 270 | 0.60 |
| 8 | 280 | 0.35 |
Interpretation of Spectrum
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The absorption band in 1,3,5-hexatriene arises due to π → π* electronic transition.
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The presence of three conjugated double bonds causes absorption at longer wavelength compared to benzene.
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This shift toward longer wavelength is known as bathochromic shift due to conjugation.
Result
The UV–Visible spectrum of 1,3,5-hexatriene was recorded and the maximum absorption wavelength (λmax) was found to be approximately 258 nm.
