Pharm-D. I -Year (Instant) Examination, January 2014
Subject : Pharmaceutical Organic Chemistry
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Time : 3 Hours Max. Marks: 70
Note: Answer All questions from Section — A and any five questions from Section — B.
Section - A (10 x 2 = 20 Marks)
- What are diasteriomers?
- What are aprotic solvents?
- What is a neucleophile?
- What is Wittig reaction?
- Outline any one method of preparation of benzyl benzoate.
- Explain why carboxylic acids are more acidic than carboxylic phenols.
- Write the structure and uses of dimercaptol.
- Explain Free radical substitution with an example.
- Draw the structures of the following molecules.
- 1, 2-dibromo-2-methylpropane
- 2, 5-dimenthylhexane
- Compare the relative acidities of acetylene, ammonia.
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Section — B (50 Marks)
- Discuss the Bayer's strain theory and explain how sache-mohr theory accounts for pit falls of Bayer's theory.
- (a) Explain the SN1 Mechanism with suitable example and give evidence.
(b) Describe the role of solvent in SN1 and SN2 reactions. - (a) Define Hukel rule. Write the common properties of aromatic compounds.
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(b) Explain theory orientation in electrophilic aromatic substitution. - Explain the detailed mechanism of Friedal-crafts alkylation and acylation reaction.
- Write Markonikov's rule and predict the products of the following reactions:
- Addition of HCl to 2-methyl-2 butene
- Addition of HBr to 1-Butuene
- Addition of HI to:2-Butene
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- Write the mechanism involved in the following reactions.
- Michael addition
- Fries rearrangement
- Write the preparation, assay and uses of following compounds.
- Salicylic acid
- Benzyl benzoate
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- Write note on :
- Kolbe reaction
- Keto-enol tautomerism
- Reformatsky reaction
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