Code No. 4253
FACULTY
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Pharm D (6 - YDC) I - Year (Main) Examination, July 2017
Subject: Pharmaceutical Organic Chemistry
Time: 3 Hours Max.Marks: 70
Note: Answer all questions from Part — A. Any Five questions from Part - B.
PART - A (10x2 = 20 Marks)
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- Write IUPAC names of the following:
- CH3 — CH— CH — COOH
|
CH3 Cl
- CH3 — CH— CH — COOH
- Explain different types of intermolecular forces.
- Write any one preparation methods of cyclopentane.
- Explain the stability of carbocations.
- Write a note on hyper conjugation.
- Write the uses of citric acid and saccharin sodium.
- Why is acetylene acidic in nature?
- Define electrophiles and nucleophiles and give examples.
- What is optical isomerism?
- What is resonance? Give examples.
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PART - B (5x10 = 50 Marks)
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- a) Explain the reaction and mechanism of Markownikoffi addition of alkene.
b) Explain Bayer’s strain theory and give its limitations. - Explain the mechanism and stereochemistry of SN1 and SN2 reactions with examples.
- a) Discuss the effect of halogen on electrophilic aromatic substitution of alkyl benzene.
b) Write the reaction and mechanism of Aldol condensation. - Explain the mechanism of E1 and E2 reactions with examples.
- Write the preparation, assay and uses of following:
- Aspirin
- Urea
- Tartaric acid
- Explain the reaction and mechanism of:
- Reformat sky reaction
- Fries Rearrangement
- Discuss the electrophilic substitution reactions of benzene with examples.
- Write notes on:
- Polarity of molecules
- Geometrical isomerism
- Acidity of phenol
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