Download PTU M-Sc -Chemistry 1st Semester May 2019 51143 ORGANIC SPECTROSCOPY Question Paper

Download PTU (I. K. Gujral Punjab Technical University) MSc -Chemistry 1st Semester May 2019 51143 ORGANIC SPECTROSCOPY Question Paper.

1 | M-51143 (S39)-1872

Roll No. Total No. of Pages : 02
Total No. of Questions : 19
M.Sc.(Chemistry) (Campus) (2015 to 2017) (Sem.-1)
ORGANIC SPECTROSCOPY
Subject Code : CHL-404
M.Code : 51143
Time : 3 Hrs. Max. Marks : 70
INSTRUCTIONS TO CANDIDATES :
1. SECTION-A is COMPULSORY consisting of TEN questions carrying TWO marks
each.
2. SECTION-B contains SIX questions carrying FIVE marks each and students
have to attempt ALL questions.
3. SECTION-C contains THREE questions carrying TEN marks each and students
have to attempt any TWO questions.

SECTION-A
1. Which is the main component of mass spectroscopy deal with resolving the ions into their
characteristics mass components according to their mass-to-charge ratio?
2. Why the magnitude of coupling constant is higher in the case of benzene rather than
cyclohexanes?
3. In which state of matter mass spectroscopy is being performed?
4. What transition is not observed by general UV-Vis spectrophtotmeter?
5. When you use CDCl
3
as a solvent in
13
C NMR, why are getting extra triplet at ~ 76 ppm?
6. How will you calculate the coupling constant in a given
1
H-NMR spectra?
7. What is the essential condition for a molecule to be IR active?
8. Write the possible electronic transitions in the benzaldehyde.
9. Why Aniline shows blue shift in acidic medium?
10. Which bond will vibrates faster between following combinations?
a) C-H or C-D
b) C-O or C-Cl
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1 | M-51143 (S39)-1872

Roll No. Total No. of Pages : 02
Total No. of Questions : 19
M.Sc.(Chemistry) (Campus) (2015 to 2017) (Sem.-1)
ORGANIC SPECTROSCOPY
Subject Code : CHL-404
M.Code : 51143
Time : 3 Hrs. Max. Marks : 70
INSTRUCTIONS TO CANDIDATES :
1. SECTION-A is COMPULSORY consisting of TEN questions carrying TWO marks
each.
2. SECTION-B contains SIX questions carrying FIVE marks each and students
have to attempt ALL questions.
3. SECTION-C contains THREE questions carrying TEN marks each and students
have to attempt any TWO questions.

SECTION-A
1. Which is the main component of mass spectroscopy deal with resolving the ions into their
characteristics mass components according to their mass-to-charge ratio?
2. Why the magnitude of coupling constant is higher in the case of benzene rather than
cyclohexanes?
3. In which state of matter mass spectroscopy is being performed?
4. What transition is not observed by general UV-Vis spectrophtotmeter?
5. When you use CDCl
3
as a solvent in
13
C NMR, why are getting extra triplet at ~ 76 ppm?
6. How will you calculate the coupling constant in a given
1
H-NMR spectra?
7. What is the essential condition for a molecule to be IR active?
8. Write the possible electronic transitions in the benzaldehyde.
9. Why Aniline shows blue shift in acidic medium?
10. Which bond will vibrates faster between following combinations?
a) C-H or C-D
b) C-O or C-Cl
2 | M-51143 (S39)-1872

SECTION-B
11. A compound C
10
H
13
Cl gave the following NMR data :
? 1.57, singlet, 6H; ? 3.07, singlet, 2H; ? 7.27, singlet, 5H. Deduce the structure of
compound.
12. Write a short note on McLefferty rearrangement.
13. How would you distinguish ethylamine, diethylamine and triethylamine using
Electronionization mass spectrometry (EI-MS) technique?
14. A compound C
10
H
14
gave the following NMR data: ? 0.88 (d, 6H); 1.86 (m, 1H); 2.45
(d, 2H); 7.12 (s, 5H). Deduce the structure of compound.
15. Write a short note on the importance of DEPTH technique in 13C NMR spectroscopy.
16. Why the intensity of N-H and O-H absorptions is stronger than C-H absorption?

SECTION-C
17. How do the following factors affect vibrational frequency in infrared spectroscopy?
a) Hydrogen bonding
b) Inductive effect and conjugation
18. Explain chemical ionization method uses in mass spectrometry. Why does chemical
ionization method give (M+1)
+
peak? Describe using chemical equations.
19. Spectral data are given below, determine the structure :
Molecular formula : C
4
H
6
O
IR frequencies in cm
?1
: 2855, 2740, 1700, 1650

1
H-NMR: 9.7 (1H, d), 6.7 (1H, dq), 6.9 (1H, dd, J=7 & 17 Hz), 2.5 (3H, d).




NOTE : Disclosure of Identity by writing Mobile No. or Making of passing request on any
page of Answer Sheet will lead to UMC against the Student.
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This post was last modified on 05 December 2019