CSIR-UGC National Eligibility Test Chemical Science Syllabus | CSIR-UGC NET Exam Pattern and Syllabus
The Joint CSIR-UGC JRF/LS (NET) Examination shall comprise 2 papers:
This paper shall be of 2 hours and 30 minutes duration and shall have a maximum of 200 marks.
Part ‘A’ of Paper I shall contain 40 General Science questions. These questions shall be common to all subject areas of NET Examination. A candidate shall be required to answer a maximum of 25 questions from Part ‘A’. In case, a candidate answers more than 25 questions, only the first 25 answered questions will be taken up for evaluation.
Part ‘B’ of Paper I shall have 100 questions. A candidate shall be required to answer a maximum of 75 questions. In case a candidate answers more than 75 questions, only the first 75 answered questions shall be evaluated. All questions shall be of two marks each. There will be negative marking for wrong answers.
This paper shall be of 2 hours and 30 minutes duration and shall have a maximum of 200 marks This Paper shall consist of 35-40 short answer type questions requiring descriptive answers. Question No. 1 shall be compulsory and carries 20 marks. In addition to the compulsory question, the candidate is required to answer a maximum of 12 questions of fifteen marks each. To answer each question, a candidate will be provided one page each.
CSIR-UGC National Eligibility Test (NET) for Junior Research Fellowship and Lecturer-ship
SYLLABUS FOR CHEMICAL SCIENCES
PAPER I AND PAPER II
1. Basic principles and applications of quantum mechanics – hydrogen atom, angular momentum.
2. Variational and perturbational methods.
3. Basics of atomic structure, electronic configuration, shapes of orbitals, hydrogen atom spectra.
4. Theoretical treatment of atomic structures and chemical bonding.
5. Chemical applications of group theory.
6. Basic principles and application of spectroscopy – rotational, vibrational, electronic, Raman, ESR, NMR.
7. Chemical thermodynamics.
8. Phase equilibria.
9. Statistical thermodynamics.
10. Chemical equilibria.
11. Electrochemistry – Nernst equation, electrode kinetics, electrical double layer, Debye-Hückel theory.
12. Chemical kinetics – empirical rate laws, Arrhenius equation, theories of reaction rates, determination of reaction mechanisms, experimental techniques
for fast reactions.
13. Concepts of catalysis.
14. Polymer chemistry. Molecular weights and their determinations. Kinetics of chain polymerization.
15. Solids – structural classification of binary and ternary compounds, diffraction techniques, bonding, thermal, electrical and magnetic properties
16. Collids and surface phenomena.
17. Data analysis.
1. Chemical periodicity
2. Structure and bonding in homo- and heteronuclear molecules, including shapes of molecules.
3. Concepts of acids and bases.
4. Chemistry of the main group elements and their compounds. Allotropy, synthesis, bonding and structure.
5. Chemistry of transition elements and coordination compounds – bonding theories, spectral and magnetic properties, reaction mechanisms.
6. Inner transition elements – spectral and magnetic properties, analytical applications.
7. Organometallic compounds – synthesis, bonding and structure, and reactivity. Organometallics in homogenous catalysis.
8. Cages and metal clusters.
9. Analytical chemistry- separation techniques. Spectroscopic electro- and thermoanalytical methods.
10. Bioinorganic chemistry – photosystems, porphyrines, metalloenzymes, oxygen transport, electron- transfer reactions, nitrogen fixation.
11. Physical characterisation of inorganic compounds by IR, Raman, NMR, EPR, Mössbauer, UV-, NQR, MS, electron spectroscopy and microscopic techniques.
12. Nuclear chemistry – nuclear reactions, fission and fusion, radio-analytical techniques and activation analysis.
1. IUPAC nomenclature of organic compounds.
2. Principles of stereochemistry, conformational analysis, isomerism and chirality.
3. Reactive intermediates and organic reaction mechanisms.
4. Concepts of aromaticity.
5. Pericyclic reactions.
6. Named reactions.
7. Transformations and rearrangements.
8. Principles and applications of organic photochemistry. Free radical reactions.
9. Reactions involving nucleophotic carbon intermediates.
10. Oxidation and reduction of functional groups.
11. Common reagents (organic, inorganic and organometallic) in organic synthesis.
12. Chemistry of natural products such as steroids, alkaloids, terpenes, peptides, carbohydrates, nucleic acids and lipids.
13. Selective organic transformations – chemoselectivity, regioselectivity, stereoselectivity, enantioselectivity. Protecting groups.
14. Chemistry of aromatic and aliphatic heterocyclic compounds.
15. Physical characterisation of organic compounds by IR, UV-, MS, and NMR.
1. Chemistry in nanoscience and technology.
2. Catalysis and green chemistry.
3. Medicinal chemistry.
4. Supramolecular chemistry.
5. Environmental chemistry.