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Q1. (a) Describe five ways of growing crystals in X-ray crystallography. (10 marks)
[Total: 20 marks]
(b) State three advantages of HPLC over the conventional chromatography. (3 marks)
(d) State five factors that affect the retention time in HPLC. (5 marks)
[Total: 20 marks]
(b) Describe three factors that affect the absorption frequency in IR spectroscopy. (6 marks)
(c) Explain how the magnetic properties of the proton arise in NMR spectroscopy. (6 marks)
(d) Explain what is meant by shielding and deshielding of hydrogen atoms in a molecule with
relevant examples. (6 marks)
[Total: 20 marks]
(b) Calculate the relative atomic mass of Z which consists of 8.7% 6Z and 91.3% of 7Z.
(2 marks)
(d) A mass spectrometer can be used to analyse organic compounds. The simplified mass
spectrum of chlorobenzene is shown in Figure 4.1.
(ii) Identify which peak belongs to the base peak in the mass spectrum. (1 mark)
(iii) Identify which peak belongs to the molecular ion peak in the mass spectrum.
(1 mark)
(iv) Write the formulae of the fragments that produce peak at m/z=112, m/z =113
m/z = 114, m/z= 115, m/z =77 and m/z= 78. (6 marks)
[Total: 20 marks]
3H
(i) How many types of proton environment are there in compound H? (1 mark)
(iv) What is the chemical shift value of the standard mentioned in (a)(ii)? (1 mark)
(v) Identify the proton and explain the splitting responsible for the peaks at 0.9 δ, 1.8
δ, 3.4 δ, and 3.9 δ in the NMR spectrum of compound H. (8 marks)
(b) An organic compound C4H5O2N is known to have two functional groups. These groups
are responsible for absorptions at 1710 cm–1, 2260 cm–1 and a broad peak at 2800 cm–1
in the infra-red spectrum of this compound.
(i) Identify the bond responsible for each of these absorptions. (3 marks)
[Total: 20 marks]