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Chemistry Coaching in Chandigarh

Chemistry Coaching in Chandigarh

Chemistry Coaching in Chandigarh – Want to learn chemistry? Join Surbhi Academy provides the best Chemistry Coaching in Chandigarh.

Surbhi Academy with a vision to provide best education for chemistry students who try to crack the Entrance exam. Surbhi Academy is the best coaching institute to offers Study Material in book Format, Online Test series, Live Classes, Recorded Classes, Video solution, Doubt Sessions, Classroom Coaching in Chandigarh. We have a very humble beginning with over years of experience in chemistry.

Chemistry Coaching in Chandigarh

Study Material + Daily Classes + 100% Results

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The Chemistry Syllabus is well taught from the lower classes as it is considered as one among the main subjects when students reach the Class 12. It is interrelated to many other topics such as physics, Biology, and Mathematics, or says something like all of these three go hand-in-hands.

The chemistry classes involve fun, application of maths, logics and more facts about the origin of life and discoveries. The Chemistry Syllabus has given below for the classes 9, 10, 11 and 12. The syllabus is everything according to the CBSE Board examination. The present CBSE syllabus is designed in such a manner so as to give a comfortable learning experience for every student.

Chemistry Coaching Classes – Surbhi Academy

Chemistry Batch has specialized classroom center where we are catering quality education in the field of chemical science. We are providing interactive leaning through technology through our smart class-room audio-visual setup which can increase the concentration of students. We keep limited students in our batches so that individual attention can be given to each and every student in order to provide quality education and better results.

“Every single day counts” so we gear up from 31st march itself, every year. Our full-time course covers everything in detail which is required not only to score well but also to clear each and every concept of chemistry.

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Do not miss the golden opportunity, to start your career for a better tomorrow.

The time span which we choose is exclusively demarcated compared to other Chemistry tuition in Chandigarh, by our experts to cover everything in detail. Be it the toughest formulas of chemistry, the trickiest equation of organic chemistry, and the trends in the periodic table; our experienced teachers beat them all with their detailed and lucid explanation, which include various exclusive tricks.

LESSONS will be conducted with different audio-visual aids and power point presentations with 3D graphics and animations for in-depth knowledge, better understanding, and long persistence of the concepts in student’s minds.

Regular test papers and discussion on previous question papers of EXAM pattern.

“Tests once conducted are meant for your learning” unlike any other chemistry tuition in Chandigarh, we strictly devote time for discussions. Each and every doubt is focused because every student is important to us. Your curiosity on every bit of a topic is something which we need.

In order to help the students, overcome the time bound pressure this chemistry coaching in chandigarh pays attention on the previous year solved question papers. So, that you can spare time to understand the strategies and level of questions being asked in the relevant examinations.

And the candid solutions are specially designed keeping in mind the mindset of a beginner, so that each one can take the benefits.

Chemistry Course Syllabus

Section 1: Physical Chemistry

Structure: Postulates of quantum mechanics. Time dependent and time independent Schrödinger equations. Born interpretation. Particle in a box. Harmonic oscillator. Rigid rotor. Hydrogen atom: atomic orbitals. Multi-electron atoms: orbital approximation. Variation and first order perturbation techniques. Chemical bonding: Valence bond theory and LCAO-MO theory. Hybrid orbitals. Applications of LCAO-MOT to H2+, H2 and other homonuclear diatomic molecules, heteronuclear diatomic molecules like HF, CO, NO, and to simple delocalized π– electron systems. Hückel approximation and its application to annular π – electron systems. Symmetry elements and operations. Point groups and character tables. Origin of selection rules for rotational, vibrational, electronic and Raman spectroscopy of diatomic and polyatomic molecules. Einstein coefficients. Relationship of transition moment integral with molar extinction coefficient and oscillator strength. Basic principles of nuclear magnetic resonance: nuclear g factor, chemical shift, nuclear coupling.

Equilibrium: Laws of thermodynamics. Standard states. Thermochemistry. Thermodynamic functions and their relationships: Gibbs-Helmholtz and Maxwell relations, van’t Hoff equation. Criteria of spontaneity and equilibrium. Absolute entropy. Partial molar quantities. Thermodynamics of mixing. Chemical potential. Fugacity, activity and activity coefficients. Chemical equilibria. Dependence of equilibrium constant on temperature and pressure. Non-ideal solutions. Ionic mobility and conductivity. Debye-Hückel limiting law. Debye-Hückel-Onsager equation. Standard electrode potentials and electrochemical cells. Potentiometric and conductometric titrations. Phase rule. ClausiusClapeyron equation. Phase diagram of one component systems: CO2, H2O, S; two component systems: liquid-vapour, liquid-liquid and solid-liquid systems. Fractional distillation. Azeotropes and eutectics. Statistical thermodynamics: microcanonical and canonical ensembles, Boltzmann distribution, partition functions and thermodynamic properties.

Kinetics: Transition state theory: Eyring equation, thermodynamic aspects. Potential energy surfaces and classical trajectories. Elementary, parallel, opposing and consecutive reactions. Steady state approximation. Mechanisms of complex reactions. Unimolecular reactions. Kinetics of polymerization and enzyme catalysis. Fast reaction kinetics: relaxation and flow methods. Kinetics of photochemical and photophysical processes.

Surfaces and Interfaces: Physisorption and chemisorption. Langmuir, Freundlich and BET isotherms. Surface catalysis: Langmuir-Hinshelwood mechanism. Surface tension, viscosity. Self-assembly. Physical chemistry of colloids, micelles and macromolecules.

Section 2: Inorganic Chemistry

Main Group Elements: Hydrides, halides, oxides, oxoacids, nitrides, sulfides – shapes and reactivity. Structure and bonding of boranes, carboranes, silicones, silicates, boron nitride, borazines and phosphazenes. Allotropes of carbon. Chemistry of noble gases, pseudohalogens, and interhalogen compounds. Acid-base concepts.

Transition Elements: Coordination chemistry – structure and isomerism, theories of bonding (VBT, CFT, and MOT). Energy level diagrams in various crystal fields, CFSE, applications of CFT, Jahn-Teller distortion. Electronic spectra of transition metal complexes: spectroscopic term symbols, selection rules, Orgel diagrams, charge-transfer spectra. Magnetic properties of transition metal complexes. Reaction mechanisms: kinetic and thermodynamic stability, substitution and redox reactions.

Lanthanides and Actinides: Recovery. Periodic properties, spectra and magnetic properties.

Organometallics: 18-Electron rule; metal-alkyl, metal-carbonyl, metal-olefin and metalcarbene complexes and metallocenes. Fluxionality in organometallic complexes. Types of organometallic reactions. Homogeneous catalysis – Hydrogenation, hydroformylation, acetic acid synthesis, metathesis and olefin oxidation. Heterogeneous catalysis – FischerTropsch reaction, Ziegler-Natta polymerization.

Radioactivity: Decay processes, half-life of radioactive elements, fission and fusion processes.

Bioinorganic Chemistry: Ion (Na+ and K+) transport, oxygen binding, transport and utilization, electron transfer reactions, nitrogen fixation, metalloenzymes containing magnesium, molybdenum, iron, cobalt, copper and zinc.

Solids: Crystal systems and lattices, Miller planes, crystal packing, crystal defects, Bragg’s law, ionic crystals, structures of AX, AX2, ABX3 type compounds, spinels, band theory, metals and semiconductors.

Instrumental Methods of Analysis: UV-visible spectrophotometry, NMR and ESR spectroscopy, mass spectrometry. Chromatography including GC and HPLC. Electroanalytical methods- polarography, cyclic voltammetry, ion-selective electrodes. Thermoanalytical methods.

Section 3: Organic Chemistry

Stereochemistry: Chirality of organic molecules with or without chiral centres and determination of their absolute configurations. Relative stereochemistry in compounds having more than one stereogenic centre. Homotopic, enantiotopic and diastereotopic atoms, groups and faces. Stereoselective and stereospecific synthesis. Conformational analysis of acyclic and cyclic compounds. Geometrical isomerism. Configurational and conformational effects, and neighbouring group participation on reactivity and selectivity/specificity.

Reaction Mechanisms: Basic mechanistic concepts – kinetic versus thermodynamic control, Hammond’s postulate and Curtin-Hammett principle. Methods of determining reaction mechanisms through identification of products, intermediates and isotopic labeling. Nucleophilic and electrophilic substitution reactions (both aromatic and aliphatic). Addition reactions to carbon-carbon and carbon-heteroatom (N,O) multiple bonds. Elimination reactions. Reactive intermediates – carbocations, carbanions, carbenes, nitrenes, arynes and free radicals. Molecular rearrangements involving electron deficient atoms.

Organic Synthesis: Synthesis, reactions, mechanisms and selectivity involving the following classes of compounds – alkenes, alkynes, arenes, alcohols, phenols, aldehydes, ketones, carboxylic acids, esters, nitriles, halides, nitro compounds, amines and amides. Uses of Mg, Li, Cu, B, Zn and Si based reagents in organic synthesis. Carbon-carbon bond formation through coupling reactions – Heck, Suzuki, Stille and Sonogoshira. Concepts of multistep synthesis – retrosynthetic analysis, strategic disconnections, synthons and synthetic equivalents. Umpolung reactivity – formyl and acyl anion equivalents. Selectivity in organic synthesis – chemo-, regio- and stereoselectivity. Protection and deprotection of functional groups. Concepts of asymmetric synthesis – resolution (including enzymatic), desymmetrization and use of chiral auxilliaries. Carbon-carbon bond forming reactions through enolates (including boron enolates), enamines and silyl enol ethers. Michael addition reaction. Stereoselective addition to C=O groups (Cram and Felkin-Anh models).

Pericyclic Reactions and Photochemistry: Electrocyclic, cycloaddition and sigmatropic reactions. Orbital correlations – FMO and PMO treatments. Photochemistry of alkenes, arenes and carbonyl compounds. Photooxidation and photoreduction. Di-π-methane rearrangement, Barton reaction. Heterocyclic Compounds: Structure, preparation, properties and reactions of furan, pyrrole, thiophene, pyridine, indole, quinoline and isoquinoline.

Biomolecules: Structure, properties and reactions of mono- and di-saccharides, physicochemical properties of amino acids, chemical synthesis of peptides, structural features of proteins, nucleic acids, steroids, terpenoids, carotenoids, and alkaloids.

Spectroscopy: Applications of UV-visible, IR, NMR and Mass spectrometry in the structural determination of organic molecules.

Contact us for Chemistry Coaching in Chandigarh

  • Surbhi Academy – Best Coaching Institute
  • SCO 54-55, 3rd Floor, Sector 34-A, Chandiagrh – India
  • +91-9915109266


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