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IV B.Tech I Semester Supplimentary Examinations, February 2008
SPECTROSCOPIC ANALYSIS OF BIOMOLECULES
(Bio-Technology)
Time: 3 hours Max Marks: 80
Answer any FIVE Questions
All Questions carry equal marks
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2. (a) What are the factors which influences the positions of absorption frequencies
form their normal value?
(b) Write a note on fermi resonance. [8+8]
3. (a) Which crystals are used for optical system infrared instruments.
(b) Write the interpretation of IR for nucleic acids. [4+12]
5. (a) Discuss broadly about the role of metal ions in biological systems and their
study by using U.V.visible spectrophotometer.
(b) Write the structures of some important chromophores. [8+8]
7. (a) Predict the appearance of the high resolution NMR spectrum of 2- hydrox-
yproponoic acid.
(b) Explain the coupling constants and their applications. [8+8]
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Code No: RR412310 Set No. 2
IV B.Tech I Semester Supplimentary Examinations, February 2008
SPECTROSCOPIC ANALYSIS OF BIOMOLECULES
(Bio-Technology)
Time: 3 hours Max Marks: 80
Answer any FIVE Questions
All Questions carry equal marks
⋆⋆⋆⋆⋆
4. (a) Detail the chemistry of electronic spectroscopy. Give the various types of
transitions involved in this technique with one example in each case.
(b) Explain the effect of polar solvents on [8+8]
i. n→ Π* and → Π* transitions.
6. “NMR spectroscopy is most important tool compared to U.V and I.R. for the
structure determination of an unknown biomolecule.” Justify this statement. [16]
7. (a) Name some important solvents used in nmr spectroscopy . What are the
important features of the solvents used in this technique.
(b) The compound with MF = C9 H10 O2 in the 1 H NMR recorded in CDCl3 /TMS
showed signals at 1.2 (t,3H), 2.8(q,2H),7.7-7.8(m,5H). Deduce the structure of
the compound. [8+8]
8. (a) What is hyperfine splitting in ESR spectroscopy? Predict the number of ESR
spectral lines expected for CH3∗ and CD3∗ radicals. Explain the relative inten-
sities in each case.
(b) Write a small note on scale of EPR. [8+8]
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Code No: RR412310 Set No. 3
IV B.Tech I Semester Supplimentary Examinations, February 2008
SPECTROSCOPIC ANALYSIS OF BIOMOLECULES
(Bio-Technology)
Time: 3 hours Max Marks: 80
Answer any FIVE Questions
All Questions carry equal marks
⋆⋆⋆⋆⋆
3. (a) Explain the different I.R peaks for the malonic acid and diethyl malonate.
(b) Explain the IR spectra for Proline and Phenyl alanine. [8+8]
6. Explain about peak area and proton counting in NMR spectra. [16]
7. Explain the NMR spectra (Signals, splitting patterns, Chemical shift values) for
the following compounds. [16]
8. (a) Sketch the ESRspectrum arising from the interaction of an unpaired electron
with three equivalent protons.
(b) Explain the importance of ESRspectra in the study of Metallo proteins. [8+8]
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Code No: RR412310 Set No. 4
IV B.Tech I Semester Supplimentary Examinations, February 2008
SPECTROSCOPIC ANALYSIS OF BIOMOLECULES
(Bio-Technology)
Time: 3 hours Max Marks: 80
Answer any FIVE Questions
All Questions carry equal marks
⋆⋆⋆⋆⋆
2. (a) Explain the electronic factors which influence the absorption frequency.
(b) How will you distinguish an aliphatic and an aromatic compound? [8+8]
3. (a) Which crystals are used for optical system infrared instruments.
(b) Write the interpretation of IR for nucleic acids. [4+12]
4. (a) Define electronic spectroscopy. What is its absorption range? Write the rela-
tionship between wavelength, frequency and wave number.
(b) Calculate the energy associated with the radiations having wave number 3 ×
104 per cm. [12+4]
7. (a) Write the NMR signals and splitting pattern for L-Proline and Phenyl alanine.
(b) A pale yellow organic compound with molecular formula C6 H5 N O3 is found
to show two signals in the nmr spectrum 1.unsymmetrical patteren multiplet
= 7.1 - 8.2 δ (4H) 2. singlet = 0.9 δ. Describe the spectrum of the compound
and explain the position of each band. [8+8]
8. Describe the role of ESR spectra in the study of Bioinorganic molecules. [16]
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