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AKTU Heterocyclic Compounds and Stereo Chemistry (Practical) (BP310P) Syllabus PDF – B.Pharm 3rd Semester

Heterocyclic Compounds and Stereo Chemistry (Practical) BP310P

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Official AKTU syllabus of Heterocyclic Compounds and Stereo Chemistry (Practical) (BP310P) for B.Pharm 3rd Semester – 2 credits, L-T-P 0-0-4. Read the unit-wise course content, course outcomes, evaluation pattern and recommended books online, or download the PDF.

Syllabus — Heterocyclic Compounds and Stereo Chemistry (Practical)

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BP310P · 2 credits · L-T-P 0-0-4

Course Objectives

  1. Understand basic laboratory safety rules and learn how to handle chemicals and glassware properly.
  2. Gain hands-on experience in preparing, purifying, and identifying organic compounds.
  3. Learn practical techniques to separate components of binary organic mixtures.
  4. Learn digital tools for drawing chemical structures and Chemical Reactions.
  5. Determine molecular properties of aromatic organic and heterocyclic compounds

Course Outcomes

COUpon successful completion of this course, the students will be able to:
No.
1Draw organic compound structures using chemical drawing tools.
2Explain and apply techniques for purification and characterization of organic compounds.
3Synthesize organic compounds through practical laboratory methods.
4Analyze and separate binary organic mixtures using suitable experimental techniques.
5Determine molecular properties of aromatic organic and heterocyclic compounds.

Course Content

List of practical (Minimum 12 experiments must be performed)

  1. Prepare, purify and characterize melting point, recrystallization following organic compounds (Minimum of 04 aromatic and any two heterocyclic compounds with different chemical reactions) a. Benzanilide/phenyl benzoate/acetanilide from aniline/ phenol by acetylation/acylation reaction. b. 2,4,6-Tribromo aniline from aniline/para bromo acetanilide from Acetanilide by halogenation (Bromination) reaction. c. 5-Nitro salicylic acid f r o m salicylic acid / meta di-nitro benzene from nitro benzene by nitration reaction. d. Benzoic acid/ Salicylic acid from alkyl benzoate/ alkyl salicylate by hydrolysis reaction. e. 1-Phenyl-azo-2-napthol from aniline by diazotization and coupling reactions. f. Synthesis of 2,4,6- trinitrophenol by nitration reaction g. Synthesis of 3,5-dimethyl pyrazole from acetylacetone. h. Synthesis of benzimidazole from ortho phenylene diamine i. Preparation of benzophenone oxime.
  2. Qualitative analysis of binary mixture of organic compounds (any two) (Acid + Neutral and Base + Neutral).
  3. To draw and visualize 3D structures, calculate molecular properties and to draw Chemical reactions using software tools

Recommended References

  1. Furniss, B. S., Hannaford, A. J., Smith, P. W. G. and Tatchell, A. R. of Practical Organic Chemistry. Pearson Education.
  2. Mann, F. G. and Saunders, B. C. Practical Organic Chemistry. Pearson Education.
  3. Pavia, D. L., Lampman, G. M. and Kriz, G. S. Introduction to Organic Laboratory Techniques: A Small Scale Approach. Brooks/Cole.

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