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Code No. 6115
FACULTY
Pharm D (6 - YDC) I - Year (Main / Backlog) Examination, August 2016
Subject: Pharmaceutical Organic Chemistry
Time: 3 Hours Max.Marks: 70
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Note: Answer all questions from Part — A. Any Five questions from Part - B.
PART - A (10x2 = 20 Marks)
- Write the IUPAC name of the following:
a) CH3—C=CH - CH =CH2
b) CH3—C—-CH2-C - CH3--- Content provided by FirstRanker.com ---
- Give the step involved in the conversion of aniline into para-nitro aniline.
- Give the structure formula of
a) Methyl-1-penten-4-yne
b) 5-Hydroxy-3-hexenal - Comment on ethanol and dimethyl ether are isomer, but differ in the boiling point.
- Briefly explain Bayer’s strain theory.
- Write the different between SN1 and SN2.
- Explain Saytzeff rule.
- Classify each of the following-nucleophil or electrophil
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1) NH3 2)H+ 3)CN- 4) Cl+ - Predict the product
i) CH3—CH = CH2 +HBr Peroxide
ii) CH3— CH = CH2 + HBr No-Peroxide - Explain Cannizzaro reaction.
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PART - B (5x10 = 50 Marks)
- Explain the nucleophillic substitution reaction with Mechanism. 10
- Explain with mechanism: 10
i) Aldol-condensation
ii) Sandmeyer’s reaction - Define rearrangement reaction. Explain mechanism of following reaction.
i) Fries rearrangement reaction
ii) Hoffman rearrangement reaction. 10 - Explain the mechanism of electrophillic substitution reaction taking a suitable example. 10
- Write the short notes on:
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i) Resonance concept
ii) Acid-Base theory. 10 - Explain mechanism involved in following reaction:
i) Kolbe reaction
ii) Michael addition 10 - a) Explain Friedel-Craft Alkylation reaction and write its drawback.
b) Write a note on activating and deactivating O, P and M directing group. - a) Explain diazo-coupling reaction with mechanism.
b) Write a note on elimination reaction:
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