Acquisition of knowledge Essay

Aims 1. To foster acquisition of knowledge and understanding of terms, concepts, facts, processes, techniques and principles relating to the defeat of interpersonal chemistry. 2. To develop the ability to apply the knowledge of contents and principles of Chemistry in new or unfamiliar situations. 3. To develop skills in proper discussion of apparatus and chemics. 4. To develop an ability to appreciate achievements in the field of Chemistry and its role in nature and society. 5. To develop an interest in activities involving usance of the knowledge of Chemistry. 6. To develop a scientific attitude through the analyse of sensual Sciences. 7. To acquaint students with the emerging frontiers and interdisciplinary aspects of the subject. 8. To develop skills relevant to the discipline. 9. To instruct students with interface of Chemistry with other disciplines of Science, much(prenominal) as, Physics, Biology, Geology, Engineering, etceteraCLASS XIThere will be two papers in the s ubject. radical I Theory- 3 hours Paper II Practical 3 hours go out Work Practical File 70 label 20 marks 7 marks 3 marks Main postulates of the theory. Its limitations. Modern pieceic theory. Laws of chemical combinations Law of conservation of biggish deed. Law of definite proportion. Law of ternionfold proportion. Law of reciprocal proportion. Gay-Lussacs law of turgidityeous the great unwasheds. Statement, explanation and bare(a) problems based on these laws. (ii) Atomic and isotopic masses. The atomic mass social unit is one of the experimentally determined unit. It is equal to 1/12 of the mass of the hundred 12 isotope. (iii) chemic equivalents, volumetric calculations in terms of normality. C = 12.00 should be taken as a standard for expressing atomic masses. equivalent lean weight expresses the combining capableness of the elements with the standard elements such as H, Cl, O, Ag, etc. variant equivalent weight. Gram equivalent weights, relationship amongst g equivalent weight, gram molecular(a) weight and valency. Determination of equivalent weight of acids, alkalis, salts, oxidising and reducing agents. (experimental details not required). 128PAPER I THEORY 70 Marks There will be one paper of 3 hours duration divided into 2 parts. Part I (20 marks) will be of compulsory shortanswer questions, testing knowledge, application and skills relating to elementary/ profound aspects of the entire syllabus. Part II (50 marks) will be divided into 3 naval divisions, A, B and C. Candidates are required to answer two out of three questions from Section A (each carrying 10 marks), two out of three questions from Section B (each carrying 5 marks) and two out of three questions from Section C (each carrying 10 marks). Therefore, a total of six questions are to be answered in Part II. SECTION A 1. Atoms and inguencules (i) The concept of atoms having fixed properties in explaining the laws of chemical combination. The study about the ato ms. Daltons atomic theoryTerms employ in volumetric calculations such as percentage (w/w and w/v), normality, molarity, molality, mole fraction, etc. should be discussed. Students are required to know the mixed bagulae. innocent calculations on the supra topics. (iv) Relative molecular mass and mole. The following methods whitethorn be considered for the determination of relative molecular masses for the gases the molar volume method Victor Meyers method (experimental details not required). mathematical problems based on the above method and Victor Meyers method. Mole concept, Avogadros recite and numerical problems on mole concept. Gram molecular volume. (v) chemical Reaction calculations based mass-volume and relationships. Self explanatory. 2. Atomic Structure (i) Electrons, Protons and Neutrons as fundamental blood cells, their charges and masses.Concept of indivisibility of atom as proposed by Dalton does not exist. The atom consists of subatomic fundamental particles. P roduction of cathode rays and their properties. Production of anode rays and their properties. Chadwicks experiment for the denudation of neutron and properties of neutron. (ii) Rutherfords nuclear model based on the scattering experiment. Rutherfords nuclear model of atom. Rutherfords scattering experiment. Discovery of nucleus. Defects of Rutherford model. (iii) Bohrs atomic model. 1. Postulates of Bohrs theory based on Plancks quantum theory. 2. Numericals on Bohrs atomic radii, velocity and competency of orbits (derivation not required). 129 Stoichiometric on mass-mass, volume-volume3. Defects in the Bohrs Model. (iv) Atomic structure wave mechanical model-a open mathematical interference. Quantum numbers shape, size and orientation of s and p orbitals precisely. Hunds rule of maximum multiplicity. Paulis exclusion principle, Aufbau principle, negatronic configuration of elements in terms of s, p, d, f subshells. Wave mechanical model experimental verification of wave nature of electron. de Broglies equation. Numericals. Heisenbergs Numericals. uncertainity principle. Quantum numbers types of quantum numbers, nurture obtained in terms of distance of electron from the nucleus, readiness of electron, number of electrons invest in an orbit and an orbital. Paulis exclusion principle. Shape, size and orientation of the s and p subshells. Hunds rule of maximum multiplicity. Aufbau principle, (n+l) rule. Electronic configuration of elements in terms of s, p, d, f subshells. 3. Periodic Table (i) Atomic number (Proton number) as the basis for classification of the elements in the Periodic Table.IUPAC nomenclature for elements with Z 100. Mendeleevs periodical law, defects in the Mendeleevs periodic mesa. Advantages and disadvantages. Modern periodic law (atomic number taken as the basis of classification of the elements). Extended and long form of periodic table. General characteristics of groups and periods. Division of periodic table as s, p, d and f blocks. (ii) Extra nuclear structure as the basis of cyclicity. more or less idea of the following ionisation total ignite, electron gain enthalpy, atomic radius, atomic volume, electronegativity, etc must be wedded. The periodicity of electronic structure leading tothe periodicity of elements e.g the relative ease of ionisation of elements. Periodic properties such as valency electrons, atomic volume, atomic and ionic radii and their variation in groups and periods. The idea of ionisation enthalpy, electron gain enthalpy and electronegativity must be given and their variation in groups and periods may be discussed. The factors (atomic number, atomic volume and shield effect, the number of electrons in the outermost orbit) which affect these periodic properties and their variation in groups and periods. (iii) Periodicity of elements with reference to s, p, d and f block elements. Classification of elements on the basis of s, p, d, f block elements and also on the basis of their distinguish and incomplete electron shells.Study of the periodicity of propertiesmentioned in point (ii) in terms of s, p, d, f blocks and the governing factors in terms of the block characteristics. 4. Chemical Bonding Electrovalent Bond (i) Electrovalent or ionic hamper e.g organic law of NaCl, Li2O, MgO, CaO, MgF2, and Na2 S. take a leak of chemical combination, octet rule, types of chemical nonpluss. Electrovalent formation of NaCl, Li2O, MgO, CaO, MgF2, and Na2S. Properties of ionic compounds. Electron window glass structure of the following ionic compounds NaCl, Li2O, MgO, CaO, MgF2, and Na2S must be taught in detail. (ii) Factors influencing the formation of ionic bond, e.g electron gain enthalpy, ionisation enthalpy, lattice skill and electronegativity. The conditions needed for the formation of ionic bonds such as low ionisation enthalpy of metals. high electron gain enthalpy of non-metals. high lattice energy. every these points must be discussed i n detail. (iii) The relation between the ionic adhere and Periodic Table. The relationship between the formation of cations and anions of the atoms and their positions in the periodic table should be discussed. Correlate the periodic property and the position of the elements in the periodic table to show the ease of formation of anions and cations and electrovalent and covalent compounds. (iv) Variable electrovalency and its vitrines. Variable electrovalency reasons for variable electrovalency i.e, due to inert electron pair effect, by apply suitable examples. Covalent Bond (i) Covalent bond, sigma and pi bonds e.g. formation of ammonia, nitrogen, ethene, ethyne, and carbon dioxide. plangency. Definition of covalent bonding, conditions for formation of covalent bonds, types of covalent bonds i.e single, double and manifold bonds. Sigma and pi bonds. H2, O2, N2. Classification of covalent bonds based on electronegativity of atoms sheertic and non cold covalent bond, dipole mo ment, formation of CH4, H2O, NH3, ethane, ethene, ethyne and CO2, etc. and their electron dot structure or Lewis structure.Characteristics of covalent compounds. Comparison in electrovalency and covalency. Resonance in simple inorganic molecules like ozone, carbon dioxide, carbonate ion and treation. (ii) Variable valency chlorine exhibits the valency of 1,3,5 & 7 respectively. Variable valency, cause of variable covalency e.g. chlorine exhibits the valency 1, 3, 5 and 7 respectively. address in terms of atomic structure. Variable covalency of phosphorus and sulphur may be discussed. Discuss in terms of atomic structure.(iii) difference of opinion from eighter from Decatur rule and Fajans rules. Definition of Octet rule. Failure of Octet rule, due to either incomplete octet or exceeding of Octet with suitable examples. Fajans rules Statements. Conditions for electrovalency and covalency must be discussed. Polar and non polar bonds should be correlated with Fajans rules.(viii) Mo lecular orbital theory, Qualitative treatment of homonuclear diatomic molecules of first two periods. Energy level diagrams, bonding, antibonding molecular orbitals, bond order, paramagnetism of O2 molecule. Relative stabilities of O2, O2-, O2- , O2+, O2++ Self-explanatory. 5. The Gaseous State (i) The gas laws, qualitatively. kinetic theory treated(iv) Co-ordinate or dative covalent bond, e.g.formation of oxy-acids of chlorine. Co-ordinate or dative covalent bonding definition, formation of hypochlorous acid, chloric acid, perchloric acid, ammonium ion, hydronium ion, nitric acid, ozone structural formulae of the above molecules based on co-ordinate bonding. (v) Hydrogen bonding its intrinsic requirements, the examples of hydrogen fluoride, urine (ice), alcohol, etc may be considered. H-bonding definition, types, condition for hydrogen bond formation, examples of inter-molecular hydrogen bonding in detail taking hydrogen fluoride, water and ice and ethanol into account. Intr amolecular hydrogen bonding.(vi) gold bonding, van der Waals forces. Metallic bonding Electron sea model and band model. Explanation of auriferous properties in terms of metallic bonding. Van der Waals forces and its types. (vii)Valence Shell Electron braces Repulsion Theory Hybridisation and shapes of molecules hybridisation involving s, p and d orbitals only sigma and pi bonds. Concept of electron-pair repulsion and shapes ofmolecules taking methane, ammonia and water as examples. Hybridisation and molecular shapes definition, hybridization of orbitals involving s, p and d orbitals (examples ethane, ethene, ethyne, PCl5 and SF6).Characteristics of gases, comparison between solid, liquid and gas. Properties of gases on the basis of kinetic theory of gases. Laws of gases Boyles Law, Charles Law, exacting Temperature, Pressure Temperature Law, Avogadros Law. Simple numerical problems based on the above laws. Postulates of Kinetic Theory must be discussed to explain gas laws. (ii) PV = nRT or PV= (w/M)RT and the application of this equation of call down. paperl gas equation PV = nRT its application in calculation of relative molecular mass and in the calculation of the look on of R.(iii) Non ideal behaviour of gases and Van der Waals equation. Non ideal behaviour of gases i.e. deviation from gas laws may be discussed at low and at high temperature and pressure. Van der Waals equation (P + a/V2) (V-b) = RT for one mole of a gas. The pressure subject area and volume correction may be explained. (iv) Daltons law, the Avogadro constant, the mole, Grahams law of spreading, simple numerical problems on the above. Daltons Law of fond(p) pressure. Application of Daltons Law. Numerical problems based on the above law. Avogadros constant. consanguinity between the mole and Avogadro number. Grahams Law of diffusion and its application. Simple numerical problems on the above.6. Colloidal Solutions Preparation and properties of colloids, both lyophilic a nd lyophobic colloids. heedlessness as evidence that the colloidal particles are charged. Idea of gold number is required, but application of gold number is not required. The importance of large surface area in adsorption should also be appreciated. doubting Thomas Graham classified the substances as crystalloid and colloid. Classification of substances on the basis of the particle size i.e. true solution, sol and suspension. Colloidal trunk is heterogeneous. Lyophilic and lyophobic colloids. Classification of colloidal solutions as micro, macro and associated colloids. Preparation of lyophilic colloids.Preparation oflyophobic colloids by colloid mill, peptisation, Bredigs arc method (procedural details not required) by oxidation, reduction, double decomposition and commuting of solvent method should be discussed. Purification of colloids (dialysis, ultra filtration, and ultracentrifugation). Properties of colloidal solutions such as Brownian movement, Tyndall effect, coagul ation and protection (protective colloids), should be discussed. Gold number and inflexible Schulze rule. Application of colloids in life. Electrophoresis (movement of dispersed phase). Emulsions, surfactants, micelles (only definition and examples).8. Chemical Energetics (i) Introduction. (a) stove of thermodynamics- characteristics of thermodynamics. (b) Types of system ideal system, real system, isolated system, closed system, open system. (c) significance of surrounding. (d) Properties of the system macroscopic, intensive and extensive properties of the system. (e) State of the system. (f) Main processes the system undergoes two-sided, irreversible, adiabatic, isothermal, isobaric, isochoric, cyclic. (g) import of thermodynamic equilibrium. (h) sum of thermodynamic process. (ii) First law of Thermodynamics mathematical statement. and its(a) Idea of conservation of energy total energy of the system and the surrounding. (b) heart of cozy energy of the system and variety in internal energy of the system. (c) convey of work do by the system and by the surrounding at constant temperature. (d) Meaning of heat cloaked by the system and by the surrounding at constant temperature. (e) The sign convention for change in internal energy, heat given out or gained, work done by the system or by the surrounding. (f) State function and raceway function- meaning with examples. (g) Internal energy change, work done and heat absorbed in a cyclic process. (h) Internal energy change in an isolated system and in non isolated system.7. Chemical Kinetics range of a chemical reaction, basic idea of order and molecularity of a reaction. target of a chemical reaction Relation between order and the stoichiometric coefficients in the balanced equation Meaning of molecularity. struggles between the order and molecularity of the reaction.Physical significance of entropy State function and not path function. Relationship between adiabatic change and entropy. Entropy chan ge of the universe and a reversible isothermal process. Entropy change of the universe and irreversible process. Meaning of thermal death. Meaning of energy content and work content ( unembellished energy) of the system thermodynamic quantity state function. Types of work and meaning of the two types of work. Meaning of Helmholtzs Free energy and Gibbs free energy and the change in Gibbs and Helmholtzs free energy.Relationship between Gibbs free energy and Helmholtzs free energy. Simple calculation on the change in Gibbs free energy and Helmholtzs free energy. Relationship between change in Gibbs free energy and equilibrium constant of a chemical reaction. Change in Gibbs free energy in reversible, irreversible, isobaric and isochoric processes. Based on change in Gibbs free energy, defining the criteria for the spontaneity of a change in terms of entropy and enthalpy defining the limits for reversible chemical reactions.(k) Chemical change and internal energy. (l) Need for enthal py constant pressure or open vessel processes. (m) Enthalpy a thermodynamic property state function. (n) Mathematical form constant pressure.(iii) Ideas about Heat, Work and Energy. Heat the energy in transit.Condition for the transfer of heat. Limitation in conversion of heat into work. Condition at which heat transfer ceases. Unit of heat. Meaning of energy capacity to do work. Meaning of work intensity factor and capacity factor. Types of work. Mathematical form of reversible work. Mathematical form of irreversible work. Difference between the reversible and irreversible work done graphically. Adiabatic reversible expansion. Relationship between Cv and internal energy change.