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I want to get the syllabus of B.Sc Life Science of the University Of Delhi. So will you provide the syllabus of B.SC Life Science Program? As you want to get the syllabus of University of Delhi in B.Sc. Life Sciences so here is the information of the same for you: Semester 1: Chemistry-I Biology-I (Introduction to Biology) Mathematics and Statistics Technical writing and Communication in English / Computational skills Semester 2: Chemistry -II Biology-II Food, Nutrition and Health Technical writing and Communication in English / Computational skills Semester 3: Chemistry -III Biodiversity-I “Microbes” Biodiversity-II “Animals” Introduction to Medical Diagnostics Semester 4: Chemistry –IV Molecular Biology Biodiversity-II “Plants” Bioinformatics Semester 5: Chemistry –V Biochemistry and Immunology Developmental Biology and Physiology-Plants Genetics & Genomics Semester 6: Chemistry –VI Applied Biology and Biotechnology Developmental Biology and Physiology-Animals Ecology and Environmental Management THEORY: Section A: Inorganic Chemistry-1 Unit 1. Atomic Structure: Recapitulation of: Bohr’s theory and its limitations, dual behaviour of matter and radiation, de-Broglie’s relation, Heisenberg Uncertainty principle. Need of a new approach to Atomic structure. What is Quantum mechanics? Time independent Schrodinger equation (H Ψ = EΨ) and meaning of various terms in it. Significance of Ψ and Ψ2, Schrodinger equation for hydrogen atom in Cartesian coordinates (x,y,z). Need of polar coordinates, transformation of Cartesian coordinates (x,y,z) into polar coordinates (r,θφ). Radial and angular parts of the hydogenic wavefunctions (atomic orbitals) and their variations for 1s, 2s, 2p, 3s, 3p and 3d orbitals. (Only graphical representation), Radial and angular nodes and their significance. Radial distribution functions and the concept of the most probable distances with special reference to 1s and 2s atomic orbitals. Significance of quantum numbers, orbital angular momentum and quantum numbers mr and ms. Shapes of s, p and d atomic orbitals, nodal planes. Discovery of spin, spin quantum number (s) and magnetic spin quantum number (ms). Rules for filling electrons in various orbitals, Electronic configurations of the atoms. Stability of half-filled and completely filled orbitals, concept of exchange energy. Relative energies of atomic orbitals, Anomalous electronic configurations Unit 2. Chemical Bonding and Molecular Structure: Ionic Bonding: General characteristics of ionic bonding. Energy considerations in ionic bonding, lattice energy and solvation energy and their importance in the context of stability and solubility of ionic compounds. Statement of Born-Lande equation for calculation of lattice energy, Born-Haber cycle and its applications, polarizing power and polarizability. Fajan’s rules, ionic character in covalent compounds, bond moment, dipole moment and percentage ionic character. Covalent bonding: VB Approach: Shapes of some inorganic molecules and ions on the basis of VSEPR and hybridization with suitable examples of linear, trigonal planar, square planar, tetrahedral, trigonal bipyramidal and octahedral arrangements. MO Approach: Rules for the LCAO method, bonding and antibonding MOs and their characteristics for s-s, s-p and p-p combination of atomic orbitals, non- bonding combination of orbitals ,MO treatment of homonuclear diatomic molecules of 1st and 2nd periods (including idea of s-p mixing) and heteronuclear diatomic molecules such as CO, NO and NO+. Comparison of VB and MO approaches. Unit 3. Fundamentals of Organic Chemistry: Physical Effects, Electronic Displacements: Inductive Effect, Electromeric Effect, Resonance and Hyperconjugation. Cleavage of Bonds: Homolysis and Heterolysis. Structure, shape and reactivity of organic molecules : Nucleophiles and electrophiles. Reactive Intermediates: Carbocations, Carbanions free radicals. Strength of organic acids and bases: Comparative study with emphasis on factors affecting pK values. Aromaticity: Benzenoids and Huckel’s rule. Unit 4. Stereochemistry: Conformations w.r.t. ethane, butane and cyclohexane. Interconversion of Wedge Formula, Newman, Sawhorse and Fischer representations. Concept of chirality (upto two carbon atoms). Configuration: Geometrical and Optical isomerism; Enantiomerism, Diastereomerism and Meso compounds) . Threo and erythro; D and L; cis - trans nomenclature; CIP Rules: R/ S (for upto 2 chiral carbon atoms) and E / Z Nomenclature (for upto two C=C systems). Unit 5. Aliphatic Hydrocarbons: Functional group approach for the following reactions (preparations & reactions) to be studied in context to their structure. For more detailed information I am uploading a PDF file which is free to download: Contact Details: University of Delhi University Road St Stephen's College, University Enclave New Delhi, Delhi 110007 India Last edited by Aakashd; May 21st, 2019 at 02:20 PM. |
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As you want to get the syllabus of the Bachelor of Science in Life Science Course of the Delhi University, so here I am providing the following Syllabus: Syllabus of B.Sc Life Science (Delhi University) 1st Semester Chemistry-I Biology-I (Introduction to Biology) Mathematics and Statistics Technical writing and Communication in English / Computational skills 2nd Semester Chemistry -II Biology-II Food, Nutrition and Health Technical writing and Communication in English / Computational skills 3rd Semester Chemistry -III Biodiversity-I “Microbes” Biodiversity-II “Animals” Introduction to Medical Diagnostics 4th Semester Chemistry –IV Molecular Biology Biodiversity-II “Plants” Bioinformatics 5th Semester Chemistry –V Biochemistry and Immunology Developmental Biology and Physiology-Plants Genetics & Genomics 6th Semester Chemistry –VI Applied Biology and Biotechnology Developmental Biology and Physiology-Animals Ecology and Environmental Management To get full syllabus, download the file……. Contact Details University Of Delhi Cavalry lane, Near Vishwavidhyalaya Metro Staion, New Delhi, DL 110007 India Tel: 011 2700 6900 Map |
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As you are asking for DU (Delhi university) B.Sc Life Science program Syllabus so on your demand I am providing same here : DU (Delhi University) B.Sc Life Science program Syllabus Paper 1-CHPT 101- Chemistry-1 (Atomic Structure, Bonding, General Organic Chemistry & Aliphatic Hydrocarbons) THEORY Marks: 100 Section A: Inorganic Chemistry-1 (30 Periods) Unit 1. Atomic Structure: Recapitulation of: Bohrs theory and its limitations, dual behaviour of matter and radiation, de-Broglies relation, Heisenberg Uncertainty principle. Need of a new approach to Atomic structure. What is Quantum mechanics? Time independent Schrodinger equation (H Ψ = EΨ) and meaning of various terms in it. Significance of Ψ and Ψ 2 , Schrodinger equation for hydrogen atom in Cartesian coordinates (x,y,z). Need of polar coordinates, transformation of Cartesian coordinates (x,y,z) into polar coordinates (r,θφ). Radial and angular parts of the hydogenic wavefunctions (atomic orbitals) and their variations for 1s, 2s, 2p, 3s, 3p and 3d orbitals. (Only graphical representation), Radial and angular nodes and their significance. Radial distribution functions and the concept of the most probable distances with special reference to 1s and 2s atomic orbitals. Significance of quantum numbers, orbital angular momentum and quantum numbers mr and ms. Shapes of s, p and d atomic orbitals, nodal planes. Discovery of spin, spin quantum number (s) and magnetic spin quantum number (ms). Rules for filling electrons in various orbitals, Electronic configurations of the atoms. Stability of half-filled and completely filled orbitals, concept of exchange energy. Relative energies of atomic orbitals, Anomalous electronic configurations. Unit 2. Chemical Bonding and Molecular Structure Ionic Bonding :General characteristics of ionic bonding. Energy considerations in ionic bonding, lattice energy and solvation energy and their importance in the context of stability and solubility of ionic compounds. Statement of Born-Lande equation for calculation of lattice energy, Born-Haber cycle and its applications, polarizing power and polarizability. Fajans rules, ionic character in covalent compounds, bond moment, dipole moment and percentage ionic character. Covalent bonding :VB Approach :Shapes of some inorganic molecules and ions on the basis of VSEPR and hybridization with suitable examples of linear, trigonal planar, square planar, tetrahedral, trigonal bipyramidal and octahedral arrangements. Concept of resonance and resonating structures in various inorganic and organic compounds. MO Approach : Rules for the LCAO method, bonding and antibonding MOs and their characteristics for s-s, s-p and p-p combination of atomic orbitals, non- bonding combination of orbitals ,MO treatment of homonuclear diatomic molecules of 1st and 2nd periods (including idea of s-p mixing) and heteronuclear diatomic molecules such as CO, NO and NO+. Comparison of VB and MO approaches. Section B: Organic Chemistry-1 (30 Periods) Unit 3. Fundamentals of Organic Chemistry Physical Effects, Electronic Displacements: Inductive Effect, Electromeric Effect, Resonance and Hyperconjugation. Cleavage of Bonds: Homolysis and Heterolysis. Structure, shape and reactivity of organic molecules : Nucleophiles and electrophiles. Reactive Intermediates: Carbocations, Carbanions free radicals. Strength of organic acids and bases: Comparative study with emphasis on factors affecting pK values. Aromaticity: Benzenoids and Huckels rule. Unit 4. Stereochemistry Conformations w.r.t. ethane, butane and cyclohexane. Interconversion of Wedge Formula, Newman, Sawhorse and Fischer representations. Concept of chirality (upto two carbon atoms). Configuration: Geometrical and Optical isomerism; Enantiomerism, Diastereomerism and Meso compounds) . Threo and erythro; D and L; cis - trans nomenclature; CIP Rules: R/ S (for upto 2 chiral carbon atoms) and E / Z Nomenclature (for upto two C=C systems). Unit 5. Aliphatic Hydrocarbons Functional group approach for the following reactions (preparations & reactions) to be studied in context to their structure. Alkanes ![]() synthesis, from Grignard reagent. Reactions: Free radical Substitution: Halogenation. Alkenes: (Upto 5 Carbons) Preparation: Elimination reactions: Dehydration of alkenes and dehydrohalogenation of alkyl halides (Saytzeffs rule); cis alkenes (Partial catalytic hydrogenation) and trans alkenes (Birch reduction). Reactions: cis-addition (alk. KMnO4) and trans-addition (bromine). Addition of HX (Markownikoffs and anti-Markownikoffs addition). Hydration, Ozonolysis, oxymecuration-demercuration, hydroboration-oxidation. Alkynes: (Upto 5 Carbons) Preparation: Acetylene from CaC2 and conversion into higher alkynes; by dehalogenation of tetra halides, dehydrohalogenation of vicinal-dihalides. Reactions: formation of metal acetylides, addition of bromine and alkaline KMnO4, ozonolysis and oxidation with hot alk. KMnO4
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