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Syllabus for CSIR-UGC National Eligibility Test (NET) CHEMICAL SCIENCES

Inorganic Chemistry:

1.Chemical periodicity2.Structure and bonding in homo-and heteronuclear molecules, including shapes ofmolecules(VSEPRTheory).

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3. Concepts of acids and bases, Hard-Soft acid base concept, Non-aqueous solvents.4.Main group elements and their compounds: Allotropy, synthesis, structure andbonding, industrial importance of the compounds.5.Transition elements and coordination compounds: structure, bonding theories,spectral and magnetic properties, reaction mechanisms.6.Inner transition elements: spectral and magnetic properties, redox chemistry,analytical applications.7.Organometallic compounds: synthesis,bonding and structure, and reactivity.Organometallics in homogeneous catalysis.8.Cages and metal clusters.9.Analytical chemistry-separation, spectroscopic, electro-and thermoanalyticalmethods.10.Bioinorganic chemistry: photosystems, porphyrins, metalloenzymes, oxygentransport, electron-transfer reactions; nitrogen fixation,metal complexes inmedicine.11.Characterisation of inorganic compounds by IR, Raman, NMR, EPR, Mössbauer,UV-vis, NQR, MS, electron spectroscopyand microscopic techniques.12.Nuclear chemistry: nuclear reactions, fission and fusion, radio-analyticaltechniques and activation analysis.

Physical Chemistry:

1.Basic principles of quantum mechanics: Postulates; operator algebra; exactly-solvable systems:particle-in-a-box, harmonic oscillator and the hydrogen atom,including shapes of atomic orbitals; orbital and spin angular momenta; tunneling.2.Approximate methods of quantum mechanics: Variational principle; perturbationtheory up to second order in energy; applications.3.Atomic structure and spectroscopy; term symbols; many-electron systems andantisymmetry principle.4.Chemical bonding in diatomics; elementary concepts of MO and VB theories;Huckel theory for conjugated π-electron systems.5.Chemical applications of group theory; symmetry elements; point groups;character tables; selection rules.6.Molecular spectroscopy: Rotational and vibrational spectra of diatomicmolecules; electronic spectra; IR and Raman activities–selection rules; basicprinciples of magnetic resonance.7.Chemical thermodynamics: Laws, state and path functions and their applications;thermodynamic description of various types of processes; Maxwell’s relations;spontaneity and equilibria; temperature and pressure dependence ofthermodynamic quantities; Le Chatelier principle; elementary description ofphase transitions; phase equilibria and phase rule; thermodynamics of ideal andnon-ideal gases, and solutions.8.Statistical thermodynamics: Boltzmann distribution; kinetic theory of gases;partition functions and their relation to thermodynamic quantities–calculationsfor model systems.9.Electrochemistry: Nernst equation, redox systems, electrochemical cells; Debye-Huckel theory; electrolytic conductance–Kohlrausch’s law and its applications;ionic equilibria; conductometric and potentiometric titrations.10.Chemical kinetics: Empirical rate laws and temperature dependence; complexreactions; steady state approximation; determination of reaction mechanisms;collision and transition state theories of rate constants; unimolecular reactions;enzyme kinetics; salt effects; homogeneous catalysis; photochemical reactions.11.Colloids and surfaces: Stability and properties of colloids; isotherms and surfacearea; heterogeneous catalysis.12.Solid state: Crystal structures; Bragg’s law and applications; band structure ofsolids.13.Polymer chemistry: Molar masses; kinetics of polymerization.14.Data analysis: Mean and standard deviation; absolute and relative errors; linearregression; covariance and correlation coefficient.

Organic Chemistry:

1.IUPAC nomenclature of organic molecules including regio-and stereoisomers.2.Principles of stereochemistry: Configurational and conformational isomerism inacyclic and cyclic compounds; stereogenicity, stereoselectivity, enantioselectivity,diastereoselectivity and asymmetric induction.3.Aromaticity: Benzenoid and non-benzenoid compounds–generation andreactions.4.Organic reactive intermediates: Generation, stability and reactivity ofcarbocations, carbanions, free radicals, carbenes, benzynes and nitrenes.5.Organic reaction mechanisms involving addition, elimination and substitutionreactions with electrophilic, nucleophilic or radical species. Determination ofreaction pathways.6.Common named reactions and rearrangements–applications in organic synthesis.7.Organic transformations and reagents: Functional group interconversion includingoxidations and reductions; common catalysts and reagents (organic, inorganic,organometallic and enzymatic). Chemo, regio and stereoselective transformations.8.Concepts in organic synthesis: Retrosynthesis, disconnection, synthons, linear andconvergent synthesis, umpolung of reactivity and protecting groups.9.Asymmetric synthesis: Chiral auxiliaries, methods of asymmetric induction–substrate, reagent and catalyst controlled reactions; determination of enantiomericand diastereomericexcess; enantio-discrimination. Resolution–optical andkinetic.10.Pericyclic reactions–electrocyclisation, cycloaddition, sigmatropicrearrangements and other related concerted reactions. Principles and applicationsof photochemical reactions in organic chemistry.11.Synthesis and reactivity of common heterocyclic compounds containing one ortwo heteroatoms (O, N, S).12.Chemistry of natural products: Carbohydrates, proteins and peptides, fatty acids,nucleic acids, terpenes, steroids and alkaloids. Biogenesis of terpenoids andalkaloids.13.Structure determination of organic compounds by IR, UV-Vis,1H&13C NMR and Mass spectroscopic techniques.

Interdisciplinary topics:

1.Chemistry in nanoscience and technology.2.Catalysis and green chemistry.3.Medicinal chemistry.4.Supramolecular chemistry.5.Environmental chemistry.

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Course Curriculum

Introduction
Introduction to CSIR UGC-NET & GATE FREE 00:00:00
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Motivation
Interview Experience 00:00:00
Private Video
Private Video Test 00:00:00
Chemical Bonding
1.0-Introduction 00:00:00
2.0-Chemical Bonding 00:00:00
5.0-Chemical Bonding 00:00:00
3.0-Chemical Bonding 00:00:00
4.0-Chemical Bonding 00:00:00
6.0-Chemical Bonding 00:00:00
7.0-Chemical Bonding 00:00:00
8.0-Chemical Bonding 00:00:00
9.0-Chemical Bonding 00:00:00
1.0-Molecular Orbital Theory 00:00:00
2.0-Molecular Orbital Theory 00:00:00
3.0-Molecular Orbital Theory 00:00:00
Organometallics
1.0-OMC 00:00:00
2.0-OMC 00:00:00
3.0-OMC 00:00:00
4.1-OMC 00:00:00
4.2-OMC 00:00:00
5.1-OMC 00:00:00
5.2-OMC 00:00:00
6.1-OMC 00:00:00
6.2-OMC 00:00:00
7.1-OMC 00:00:00
7.2-OMC 00:00:00
7.3-OMC 00:00:00
8.0-OMC 00:00:00
9.1-OMC 00:00:00
9.2-OMC 00:00:00
9.3-OMC 00:00:00
10.1-OMC 00:00:00
10.2-OMC 00:00:00
11.1-OMC 00:00:00
11.2-OMC 00:00:00
12.1-OMC 00:00:00
12.2-OMC 00:00:00
13.1-OMC 00:00:00
13.2-OMC 00:00:00
14.2-OMC 00:00:00
14.1-OMC 00:00:00
15-OMC 00:00:00
16-OMC 00:00:00
17.1-OMC 00:00:00
17.2-OMC 00:00:00
18.1-OMC 00:00:00
18.2-OMC 00:00:00
19.0-OMC 00:00:00
20-OMC 00:00:00
21-OMC 00:00:00
22.1-OMC 00:00:00
22.2-OMC 00:00:00
22.3-OMC 00:00:00
OMC Previous Year Questions Part-1 00:00:00
OMC Previous Year Questions (Part-2) 00:00:00
Chemical Kinetics
1.0-Chemical Kinetics 00:00:00
2.0-Chemical Knietics 00:00:00
3.0-Chemical Kinetics 00:00:00
3.1-Chemical Kinetics 00:00:00
4.0-Chemical Kinetics 00:00:00
5.0-Chemical Kinetics 00:00:00
6.0-Chemical Kinetics 00:00:00
7.1-Chemical Kinetics 00:00:00
7.2-Chemical Kinetics 00:00:00
7.3-Chemical Kinetics 00:00:00
8.1-Chemical Kinetics 00:00:00
8.2-Chemical Kinetics 00:00:00
8.3-Chemical Kinetics 00:00:00
9.1-Chemical Kinetics 00:00:00
9.2-Chemical kinetics 00:00:00
9.3-Chemical Kinetics 00:00:00
10.1-Chemical Kinetics 00:00:00
10.2-Chemical Kinetics 00:00:00
10.3- Chemical kinetics 00:00:00
11.1-Chemical Kinetics 00:00:00
11.2-Chemical Kinetics (Photochemistry) 00:00:00
11.3-Chemical Kinetics (Photochemistry) 00:00:00
Reaction Mechanism
1.0-Reaction Mechanism 00:00:00
2.0-Reaction Mechanism 00:00:00
3.0-Reaction Mechanism 00:00:00
4.0-Reaction Mechanism 00:00:00
5.0-Reaction Mechanism 00:00:00
6.0-Reaction Mechanism 00:00:00
7.0-Reaction Mechanism 00:00:00
8.0-Reaction Mechanism 00:00:00
8.1-Reaction Mechanism 00:00:00
9-Reaction Mechanism 00:00:00
StereoChemistry
1.0-StereoChemistry 00:00:00
2.0-StereoChemistry 00:00:00
3.0-StreoChemistry 00:00:00
4.0-StereoChemistry 00:00:00
5.0-StereoChemistry 00:00:00
6.0-StereoChemistry 00:00:00
7.0-Stereochemistrty 00:00:00
8.0-Stereochemistry 00:00:00
9.0-Stereochemistry 00:00:00
10-Stereochemistry 00:00:00
11-Stereochemistry 00:00:00
NMR Spectroscopy
Introduction to Spectroscopy 00:00:00
1-NMR Spectroscopy 00:00:00
2.0-NMR Spectroscopy 00:00:00
3.0-NMR Spectroscopy 00:00:00
4.0-NMR Spectroscopy 00:00:00
5.0-NMR Spectroscopy 00:00:00
6.0-NMR Spectroscopy 00:00:00
7.0-NMR Spectroscopy 00:00:00
8.0-NMR Spectroscopy 00:00:00
9.0-NMR Spectroscopy 00:00:00
10.0-NMR Spectroscopy 00:00:00
11.0-NMR Spectroscopy 00:00:00
12.0-NMR Spectroscopy 00:00:00
13.0-NMR Spectroscopy 00:00:00
14.1-NMR Spectroscopy 00:00:00
14.2-NMR Spectroscopy 00:00:00
15.0-NMR Spectroscopy 00:00:00
NMR Assignment-1 Solution 00:00:00
NMR Previous year solution-1 00:00:00
Pericyclic Reactions
1.0-Pericyclic 00:00:00
2.0-Pericyclic (ElectroCyclic Reactions) 00:00:00
3.0-PeriCyclic(ElectroCyclic-2) 00:00:00
4.0-Pericyclic Reaction 00:00:00
5.0-Pericyclic Reaction 00:00:00
6.0-Pericyclic reactions 00:00:00
7.0-Pericyclic 00:00:00
8.0-Pericyclic 00:00:00
9.1-Pericyclic 00:00:00
9.2-PeriCyclic 00:00:00
10.1-PeriCyclic 00:00:00
10.2-Pericyclic 00:00:00
11.1- Pericyclic Reaction 00:00:00
11.2-pericyclic 00:00:00
12.1-Pericyclic 00:00:00
12.2-Pericyclic 00:00:00
13.1-Pericyclic 00:00:00
13.2-Pericyclic Reactions 00:00:00
14.1-Pericyclic 00:00:00
14.2-Pericyclic 00:00:00
15.1-Pericyclic 00:00:00
15.2-Pericyclic 00:00:00
16.1-Pericyclic 00:00:00
16.2- Pericyclic Reactions 00:00:00
General Organic Chemistry
1.0 GOC 00:00:00
2.0 GOC 00:00:00
3.0 GOC 00:00:00
4.0 GOC 00:00:00
5.0 GOC 00:00:00
6.0 GOC 00:00:00
Aromaticity
Aromaticity-1 00:00:00
Aromaticity-2 00:00:00
Aromaticity-3 00:00:00
Reactive intermediates
1-Reactive intermediate 00:00:00
2-Reactive intermediate 00:00:00
3-R.I. 00:00:00
4-R.I. 00:00:00
5-R.I 00:00:00
6-R.I. 00:00:00
7-R.I. 00:00:00
Thermodynamics
1.0-Thermo 00:00:00
2.0-Thermo 00:00:00
3.0-Thermo 00:00:00
4.0-Thermo 00:00:00
5.0-Thermodynamics 00:00:00
6.0-Thermodynamics 00:00:00
7.1-Chemical Thermodynamics 00:00:00
7.2-Chemical Thermodynamics 00:00:00
8.0-Chemical Thermodynamics 00:00:00
9.0-Chemical Thermodynamics 00:00:00
10-Chemical Thermodynamics 00:00:00
11.0-Thermodynamics 00:00:00
12.0-Chemical Thermodynamics 00:00:00
ElectroChemistry
1.0-Elcrochemistry 00:00:00
2.0-Electrochemistry 00:00:00
3.0-Electrochemistry 00:00:00
4.0-Electrochemistry 00:00:00
5.0-Electrochemistry 00:00:00
6.0-Electrochemistry 00:00:00
7.0-Electrochemistry 00:00:00
8.0-Electrochemistry 00:00:00
9.0-Electrochemistry 00:00:00
10.0-Electrochemistry 00:00:00
11.0- Electrochemistry 00:00:00
12.0- Electrochemistry 00:00:00
13.0-Electrochemistry 00:00:00
14.0-Electrochemistry 00:00:00
Reagent
1.0-Reagent 00:00:00
2.0-Reagent 00:00:00
3.0-Reagent 00:00:00
40-Reagent 00:00:00
5.0-Reagent 00:00:00
6.0-Reagent 00:00:00
7.0-Reagent 00:00:00
8.0-Reagent 00:00:00
9.0-Reagent 00:00:00
Coordination Chemistry
1.0-Coordination 00:00:00
2.0-Coordination 00:00:00
3.0-Coordination 00:00:00
4.0-Coordination 00:00:00
4.1-Coordination 00:00:00
5.0-Coordination 00:00:00
6.0-Coordination 00:00:00
7.0-Coordination 00:00:00
8.0-Coordinationn 00:00:00
9.0-Coordination 00:00:00
10-Coordintion 00:00:00
11-Cordination 00:00:00
12-Coordination 00:00:00
13-Coordination 00:00:00
14-Coordination 00:00:00
15-Coordination 00:00:00
16-Coordination 00:00:00
17-Coordination 00:00:00
18-Coordination 00:00:00
Quantum Chemistry
1.0- Quantum chemistry 00:00:00
2.0- Quantum Chemistry 00:00:00
3.0- Quantum Chemistry 00:00:00
4.0- Quantum Chemistry 00:00:00
5.0- Quantum Chemistry 00:00:00
6.0- Quantum Chemistry 00:00:00
7.0- Quantum Chemistry 00:00:00
8.0- Quantum Chemistry 00:00:00
9.0- Quantum chemistry 00:00:00
10.0- Quantum chemistry 00:00:00
11.0- Quantum Chemistry 00:00:00
12.0- Quantum Chemistry 00:00:00
13.0- Quantum chemistry 00:00:00
14.0- Quantum Chemistry 00:00:00
15.0- Quantum Chemistry 00:00:00
16.0-Quantum Chemistry 00:00:00
17.0-Quantum Chemistry 00:00:00
18.0-Quantum Chemistry 00:00:00
19.0-Quantum Chemistry 00:00:00
20.0-Quantum Chemistry(Bohr’s Model of Hydrogen like atoms) 00:00:00
21.0-Quantum Chemistry 00:00:00
22.0-Quantum Chemistry 00:00:00
23.0-Quantum Chemistry 00:00:00
24.0-Quantum chemistry 00:00:00
25.0-Quantum Chemistry 00:00:00
26.0-Quantum Chemistry 00:00:00
27.0-Quantum Chemistry ( Superposition principle) 00:00:00
Periodicity
Periodicity-01 00:00:00
2.0- Periodicity 00:00:00
Name Reaction
1.0- Name Reaction 00:00:00
2.0- Name Reaction 00:00:00
3.1- Name Reaction 00:00:00
3.2- Name Reaction 00:00:00
4.0- Name Reaction 00:00:00
5.0- Name Reaction 00:00:00
6.0- Name Reaction 00:00:00
7.0- Name Reaction 00:00:00
8.0- Name Reaction 00:00:00
9.0- Name Reaction 00:00:00
10.0- Name Reaction 00:00:00
11.0- Name Reaction 00:00:00
12-Name Reaction ( DAKIN OXIDATION ) 00:00:00
13-Name Reaction ( Favorskii Rearrangment ) 00:00:00
14-Name Reaction (Wegner Merwein Rearrangment ) 00:00:00
15- Name Reaction (Pinacol Semipinacol Rearrangment 00:00:00
16-Name Reaction ( Dienone-Phenol Rearrangment ) 00:00:00
17-Name Reaction (Benzilic Acid Rearrangment) 00:00:00
18-Name Reaction( Benzoin & Darzen Condensation & Haffmann Rearrangment ) 00:00:00
19-Name Reaction( CURTIUS REARRANGMENT ) 00:00:00
20-Name Reaction( Schmidt Rearrangement ) 00:00:00
21-Name Reaction ( Mc-MURRY Coupling ) 00:00:00
22-Name Reaction ( Enloate Chemistry ) 00:00:00
23-Name Reaction 00:00:00
Last Name Reaction 00:00:00
Main Group Chemistry
1.0-Main Group Chemistry 00:00:00
2.0-Main Group Chemistry 00:00:00
3.0-Main Group Chemistry 00:00:00
4.0-Main Group Chemistry 00:00:00
5.0-Main Group Chemistry 00:00:00
6.0-Main Group Chemistry 00:00:00
7.0- Main group Chemistry 00:00:00
8.0 Main group 00:00:00
9.0-Main Group 00:00:00
10-Main Group ( Oxygen Family ) 00:00:00
Hetrocyclic Compounds
Part-01 00:00:00
Part-02 00:00:00
Part-03 00:00:00
Bio-Inorganic Chemistry
1.0-Bioinorganic Chemistry 00:00:00
2.0-Bioinorganic Chemistry 00:00:00
3.0 -Bioinorganic chemishtry 00:00:00
4.0- Bioinorganic chemishtry 00:00:00
5.0- Bio-inorganic 00:00:00
6.0- Bio-inorganic 00:00:00
7.0-Bio-Inorganic 00:00:00
8.0-BioInorganic Chemistry 00:00:00
9.0-BioInorganic Chemistry 00:00:00
10.0-BioInorganic Chemistry 00:00:00
11.0-Bioinorganic 00:00:00
IR Spectroscopy (organic)
1.0-IR Spectroscopy 00:00:00
2.1-IR Spectroscopy 00:00:00
2.2-IR Spectroscopy 00:00:00
F- Block
1.0 F-Block 00:00:00
2.0 F- Block 00:00:00
3.0 F-Block 00:00:00
Chemical Equilibrium
1.0 -Chemical Equilibrium 00:00:00
2.0 -Chemical Equilibrium 00:00:00
3.0 -Chemical Equilibrium 00:00:00
4.0-Chemical Equilibrium 00:00:00
5.0-Chemical Equilibrium 00:00:00
6.0-Chemical Equilibrium 00:00:00
7.0-Chemical Equilibrium 00:00:00
8.0-Chemical Equilibrium 00:00:00
9.1-Chemical Equilibrium 00:00:00
Amino Acids
Part-1 00:00:00
Amino Acids Part-02 00:00:00
Polymer Chemistry
polymer chemistry 00:00:00
Group Theory
Group Theory Lec-01 00:00:00
Group Theory Lec-02 00:00:00
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