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The document provides answers to critical thinking questions about spectroscopy techniques for identifying organic molecules, including infrared (IR) spectroscopy, UV-visible spectroscopy, proton nuclear magnetic resonance (1H NMR) spectroscopy, and mass spectrometry. It examines concepts like chemical shifts, coupling, integration, and fragmentation patterns. Sample molecules are used to demonstrate how to analyze spectra and deduce structural information.

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438 views

Ws10 Answers

The document provides answers to critical thinking questions about spectroscopy techniques for identifying organic molecules, including infrared (IR) spectroscopy, UV-visible spectroscopy, proton nuclear magnetic resonance (1H NMR) spectroscopy, and mass spectrometry. It examines concepts like chemical shifts, coupling, integration, and fragmentation patterns. Sample molecules are used to demonstrate how to analyze spectra and deduce structural information.

Uploaded by

Kassim
Copyright
© © All Rights Reserved
Available Formats
Download as PDF, TXT or read online on Scribd
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CHEM1405 Spectroscopy Workshop – Answers to Critical Thinking Questions

The worksheets are available in the tutorials and form an integral part of the learning outcomes and
experience for this unit.

Model 1: Infrared (IR) Spectroscopy

1. See below.

Model 2: UV-Visible Spectroscopy


1. See below.

2. All of the above.


3. Restricted to the identification of conjugation.
Model 3: 1H NMR Spectroscopy - Chemical Shifts
1. The molecule on the left has 3 types of H atom and the molecule on the right has 7 types of H atom.

2. The molecule on the left will give 3 signals and the molecule on the right will give 7 signals.
3.

Model 4: 1H NMR Spectroscopy - Coupling


1. Number of peaks = n + 1 where n is the number of hydrogen atoms on adjacent atoms which are not
equivalent to the 1H giving rise to the signal.
2. None, or the adjacent hydrogen atoms are in the same environment (equivalent).
3. A septet with intensity ratio 1: 6 : 15 : 20 : 15 : 6 : 1.

Model 5: 1H NMR Spectroscopy - Integration


1. There are 3 signals due to the 3 types of 1H environment: A, B and C.
The signal at 1.3 ppm is due to the 6 1H in environment A:
relative integral = 3. The signal is split into a 1:2:1 triplet due
to coupling to the 2 1H on the neighbouring CH2 group (B).
The signal at 4.5 ppm is due to the 4 1H in environment B:
relative integral = 2. The signal has a higher chemical shift
than that for group A due to the presence of the
electronegative O atom. The signal is split into a 1:3:3:1
quartet due to coupling to the 3 1H on the neighbouring CH3
group (A).
The signal at ~5.3 ppm is due to the 2 1H in environment C: relative integral = 1. The signal has a
higher chemical shift than that for group A or B as the 1H atoms are on a sp2 C atom that is bonded to
an electronegative O atom. There are no 1H on the neighbouring atoms, except the other equivalent
1
H atom, so no splitting due to coupling is observed.
Note that the relative number of hydrogen atoms in each environment given by the integration is
3:2:1, but the actual number of hydrogen atoms is 6:4:2.

2. There are 3 signals due to the 3 types of 1H environment: A, B and C.


The signal at ~1.1 ppm is due to the 3 1H in environment A: integral = 3. The
signal is split into a 1:2:1 triplet due to coupling to the 2 1H on the
neighbouring CH2 group (C).
The signal at 2.1 ppm is due to the 3 1H in environment B: integral = 3. The
signal has a higher chemical shift than that for group A due to the presence of
the electronegative O atom. There are no 1H on the neighbouring atoms, so no
splitting due to coupling is observed.
The signal at ~2.5 ppm is due to the 2 1H in environment C: integral = 2. The signal has a higher
chemical shift than that for group A due to the presence of the electronegative O atom. The signal is
split into a 1:3:3:1 quartet due to coupling to the 3 1H on the neighbouring CH3 group (A).

3. HB have the highest shift since they are closest to the electronegative O atoms. There are two HB
atoms so the signal has an integral of 2. The HB atoms are coupling to 3 × HC atoms giving rise to a
(n + 1) = (3 + 1) = 4 line multiplet (a quartet).
HC have the lowest shift since they are further from the electronegative O atoms. There are three HB
atoms so the signal has an integral of 3. The HC atoms are coupling to 2 × HB atoms giving rise to a
(n + 1) = (2 + 1) = 3 line multiplet (a triplet).

HA, singlet,
Integration = 3

HC, triplet,
HB, quartet, Integration = 3
Integration = 2

5 4 3 2 1 0
PPM

Model 6: Mass Spectrometry

1. m/z Fragment
99 M+ peak: containing one 13C (1% chance).
98 Molecular ion – C6H10O
83 C5H7O (loss of –CH3 - 15 mass units)
55 C4H7 (loss of –CH3CO - 43 mass units)
43 C3H7 (loss –of CH3COC – 45 mass units)
39 C3H
29 CHO or C2H4

2. Acetonitrile: CH3C≡N.

Model 7: Combined Use of Mass Spectrometry and IR, UV-Visible and NMR
Spectroscopy to Identify Unknown Compounds.
1. 3-methylbutan-2-one:
2. 2-bromoethyl acetate:

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