1. This document outlines the syllabus for a Bachelor of Science in Chemistry program over four semesters. It details the courses, topics, textbooks, and laboratory experiments for Physical Chemistry, Inorganic Chemistry, and Organic Chemistry.
2. Semesters I and II cover Physical and Inorganic Chemistry topics like thermodynamics, chemical kinetics, atomic structure, and bonding models. Semesters I and III additionally cover Organic Chemistry topics like structure and reactions of alkanes, alkenes, alkynes, and spectroscopy.
3. The laboratory components involve experiments in physical chemistry like reaction kinetics, in inorganic qualitative analysis, and in organic techniques like crystallization, distillation, and qualitative organic analysis
This document provides a detailed syllabus for the Physical Organic Chemistry course in the B.Pharm program. It outlines 6 topics that will be covered over the semester for a total of 45 hours. These include introduction to bonding concepts, modern theories of organic bonding, kinetics and reaction mechanisms, acid-base catalysis, and charge transfer complexes and reactions. For each topic, it lists the sub-topics and number of hours allocated. It also provides 5 reference books for the course.
The document then provides syllabus details for other semester 1 courses including Physical Pharmacy I, Anatomy Physiology and Pathophysiology I, Environmental Science, Communication Skills, and Physical Pharmacy Laboratory I. It outlines the topics,
This document outlines the compulsory courses for chemistry degrees at the University of Peradeniya in Sri Lanka. It lists the core courses required for both the general and special degrees in chemistry. It also provides details on 100-level introductory courses covering topics like principles of chemistry, qualitative and quantitative analysis labs, and organic functional group analysis. Recommended textbooks are provided for further reference on course topics like physical chemistry, organic chemistry, and laboratory techniques.
This chapter discusses carbocations, which are positively charged carbon-containing ions that are highly reactive intermediates in organic chemistry. Carbocations have six electrons in the outer shell of the central carbon atom. They are stabilized by electron-donating groups and destabilized by electron-withdrawing groups. Carbocations undergo various reactions including reactions with nucleophiles, elimination reactions, rearrangement reactions, and additions to unsaturated systems. Non-classical carbocations are also discussed.
Introduction of University Chemistry Syllabus B. Sc.-III (Sem-VI) Session 202...pramod padole
Ìý
This PowerPoint presentation introduces the B.Sc. Sem-VI chemistry syllabus at Shri Shivaji Science College in Amravati, India. It covers 6 units: inorganic chemistry, organic chemistry, physical chemistry, and elementary quantum mechanics. The inorganic chemistry units cover topics like kinetics of metal complexes, analytical chemistry techniques like spectroscopy and chromatography. The organic chemistry units cover spectroscopy techniques like electronic, infrared, and NMR spectroscopy and mass spectrometry. The physical chemistry units cover elementary quantum mechanics, electrochemistry, and nuclear chemistry.
Introduction of University Chemistry Syllabus of B. Sc.-Part-I (Sem-II) by Dr...pramod padole
Ìý
This document provides an overview of the B.Sc. Part I Semester II chemistry syllabus taught by Dr. Pramod R. Padole at Shri Shivaji Science College in Amravati, India. The syllabus covers inorganic chemistry, organic chemistry, and physical chemistry units. For inorganic chemistry, the units cover topics like polarization, covalent bonding, acids and bases, p-block elements, noble gases, and non-aqueous solvents. The organic chemistry units discuss alkenyl halides, aryl halides, alcohols, phenols, ethers, and epoxides. Finally, the physical chemistry units focus on physical properties and molecular structure, and chemical kinetics.
Chapter 03 organic compounds alkanes and cycloalkanesWong Hsiung
Ìý
This document provides an overview of organic compounds called alkanes and cycloalkanes. It defines key terms like functional groups and discusses different types of organic compounds grouped by their functional groups, including alkenes, alkynes, and arenes. The document also covers properties and naming conventions for alkanes and cycloalkanes specifically. It describes structural isomers and cis-trans isomerism that can occur in cycloalkane compounds.
Chapter 05 stereochemistry at tetrahedral centersWong Hsiung
Ìý
This document discusses stereochemistry at tetrahedral carbons. It defines key terms like enantiomers, which are nonsuperimposable mirror images of each other. Enantiomers have different spatial arrangements but identical physical properties except for how they rotate plane-polarized light. The document also outlines Cahn-Ingold-Prelog rules for assigning R and S configurations to chiral centers based on atomic number priorities. Diastereomers are stereoisomers that are not mirror images, while meso compounds have chiral centers but are achiral due to an internal plane of symmetry.
1. The document discusses the basics of organic chemistry including nomenclature of organic compounds, functional groups, molecular structure and bonding.
2. Key concepts covered include IUPAC naming rules, identifying primary, secondary and tertiary carbons, common functional groups, covalent and ionic bonding, and molecular orbital theory.
3. Bond polarity is discussed, noting that bonds between carbon and more electronegative atoms like oxygen are polarized with partial positive and negative charges.
Introduction of Chemistry Syllabus of B. Sc. Part-I (Semester-II) by Dr Pram...pramod padole
Ìý
This document provides an introduction to the B.Sc. Part I Semester II chemistry syllabus from Shri Shivaji Science College in Amravati, India. It outlines the six units that will be covered: inorganic chemistry (units I-II), organic chemistry (units III-IV), and physical chemistry (units V-VI). Each unit is briefly described, including topics like polarisation, covalent bonding, acids and bases (unit I), p-block elements, noble gases, and non-aqueous solvents (unit II). Contact information is provided for questions.
This document provides an outline for teaching organic chemistry. It covers general principles like hybridization and bond properties. It then discusses specific classes of compounds like alkanes, alkenes, alkynes, alcohols, alkyl halides, aldehydes, ketones, carboxylic acids and their derivatives. Protection and deprotection of functional groups is introduced. The document also covers aromaticity, aromatic compounds, heterocyclic compounds, carbohydrates, amino acids, proteins, and pericyclic reactions. Specific reactions involving carbonyl groups are also detailed along with stereochemistry.
Chapter 2 polar covalent bonds acids and basesWong Hsiung
Ìý
This document summarizes key concepts about polar covalent bonds and acid-base chemistry from Chapter 2 of an organic chemistry textbook. It discusses how electronegativity differences between atoms lead to polar covalent bonds and molecular polarity. Bond polarity is quantified using dipole moments. The Brønsted-Lowry definition of acids and bases in terms of proton transfer is introduced. Acid strength is described using acid dissociation constants (Ka) and their pKa values. Factors that influence acid and base strength are also covered.
1) Organic chemistry is the study of carbon compounds and their properties. It is a separate discipline due to the vast number and variety of organic compounds, many of which are essential to life.
2) Carbon can form chains and rings by bonding to itself and other elements like hydrogen, oxygen, nitrogen and halogens. Functional groups like alcohols, aldehydes, ketones and carboxylic acids determine the properties and reactivity of organic molecules.
3) Chiral molecules are non-superimposable mirror images called enantiomers that can have different biological effects. The R/S system is used to distinguish these two forms.
This document outlines the syllabus for chemistry for class 11 in India. It includes:
1. The topics to be covered in terms 1 and 2, such as atomic structure, chemical bonding, redox reactions, and organic chemistry.
2. The number of periods and marks allocated for each topic.
3. Details of the practical exams to be conducted each term, involving volumetric analysis, salt analysis, and other experiments.
4. Guidelines for evaluating visually handicapped students in practical exams by rationalizing the syllabus.
1. The document discusses organic chemistry, which involves the study of carbon-containing compounds. It covers topics such as classification of organic molecules, structural representation, functional groups, and reaction types.
2. Organic compounds are classified as aliphatic, heterocyclic, and homocyclic compounds. Structural formulas are used to represent organic molecules, including complete, condensed, and bond line formulas.
3. Functional groups determine properties of organic compounds. Reaction types covered include substitution, addition, elimination, and rearrangement reactions.
This document discusses inductive effects, resonance, and hyperconjugation. It defines resonance structures as alternative arrangements of electrons that stabilize molecules, and describes how resonance hybrids depict delocalized electrons. It explains that inductive effects stabilize charges through sigma bond polarization from electronegative atoms. Finally, it describes how hyperconjugation delocalizes positive charges in carbocations through overlap of vacant p orbitals with adjacent carbon-hydrogen sigma bonds.
This document provides information about a textbook on organic chemistry. It was published in 2004 as the second edition. The textbook aims to provide comprehensive yet concise basic notes on core topics of organic chemistry for undergraduate students. It focuses on the essential concepts across 15 sections, condensing the material into 310 pages to make it more manageable for students compared to larger textbooks. The goal is for students to understand reaction mechanisms, which brings logic and clarity to remembering reactions of different functional groups.
Chapter 06 an overview of organic reactions Wong Hsiung
Ìý
This document discusses organic reaction mechanisms. It explains that reactions occur through a series of steps, and may involve intermediates that are neither the starting reactants nor final products. Polar reactions involve the combination of electrophiles and nucleophiles, while radical reactions involve the formation and reaction of free radicals. The mechanism of HBr addition to ethylene is used as an example, involving the carbocation intermediate. Reaction steps and intermediates are illustrated using energy diagrams, and factors like bond energies and transition states are also discussed.
COMPREHENSIVE HANDOUT FOR ORGANIC CHEMISTRYPaolo Naguit
Ìý
This document provides an overview of organic chemistry nomenclature and structural formulas. It discusses the different types of structural formulas used to depict organic molecule structures, including straight-line, condensed, 3D, and skeletal formulas. It also outlines the IUPAC rules for systematic nomenclature, including naming conventions for functional groups, prefixes, parents, locants, and suffixes. Key aspects covered include priority rules for determining the parent chain and functional group that occupies the suffix. Functional groups are organized by priority in a table with their corresponding prefixes and suffixes. Naming conventions are also discussed for classes of organic compounds including alkanes, alkyl halides, alkenes and alkynes.
Organic compounds are vital for life and include substances like DNA, proteins, fuels, polymers, dyes, and medicines. Carbon has the unique ability to form covalent bonds with itself and other elements through a process called catenation. The shapes of organic molecules like methane, ethene, and ethyne are determined by the hybridization of carbon - methane is tetrahedral due to sp3 hybridization, ethene is planar due to sp2 hybridization, and ethyne is linear due to sp hybridization. Hybridization also influences bond lengths and energies. π-bonds form through parallel sideways overlap of p-orbitals on adjacent carbons and have electron density above and below the plane of the bonded atoms
The document discusses chirality in heteroatom systems where chirality arises from a non-carbon centre. It explains that compounds containing nitrogen, phosphorus, sulfur or other atoms can exhibit stereochemistry when the atom forms a tetrahedral structure with four different groups. The stereochemistry of these compounds provides useful information for drug applications. It then focuses on the specific stereochemistry of various nitrogen, phosphorus and sulfur compounds, including amines, oximes, azo compounds, phosphines and sulfoxides. It describes how these compounds can exhibit geometrical isomers, inversion barriers, and retention or inversion of configuration under chemical reactions.
The document provides a year-at-a-glance pacing guide for a Chemistry I course. It outlines the major topics to be covered in each of the four nine-week periods, including: introduction to chemistry, matter and energy, the periodic table, chemical bonding and molecular structures in the first period; nomenclature and formulas, chemical reactions, the mole, and stoichiometry in the second period; states of matter, solutions, acids and bases in the third period; and reaction rates, gas laws, nuclear chemistry, energy and chemical change, and an introduction to organic chemistry in the fourth period.
This document provides information about the Organic Chemistry CHEM 230 course. It includes details about the instructor, course objectives, content, textbooks, grading breakdown, and Chapter 1 topics. The key points are:
1. The course is taught by Dr. Suzan Abdulrahman Khiyat and covers the theoretical and experimental basis of organic chemistry for non-chemistry students.
2. Chapter 1 topics include carbon compounds and chemical bonds, isomers, 3D shapes of molecules, electronegativity, and resonance.
3. Student evaluation is based on two midterms, a lab, and a final exam, totaling 100 points.
Optical activity in catenanes and rotaxanesPRUTHVIRAJ K
Ìý
These class of compounds do not contain any formal chiral centre but exhibit stereoisomerism due to presence of either a chiral axis or a chiral plane and are called stereoaxis and stereoplanes respectively
This document provides an outline for topics to be discussed in an organic chemistry tutorial, including: introduction to organic chemistry; nomenclature; carbon properties including hybridization and bonds; isomers and stereochemistry; chirality of molecules including conformational and configurational isomers; and relative and absolute configuration. The tutorial will cover key organic chemistry concepts such as naming organic compounds, identifying isomers, hybridization principles, and the 3D arrangement of atoms in chiral molecules.
The document provides an overview of the chemistry syllabus for JAM 2022, covering both physical chemistry and organic chemistry topics. It includes sections on atomic and molecular structure, the gaseous state, chemical thermodynamics, chemical kinetics, spectroscopy, and inorganic chemistry topics like periodic properties, transition metals, and main group elements. The syllabus also covers organic reaction mechanisms, natural products, aromatic compounds, qualitative organic analysis, and instrumental methods of analysis.
This document provides the syllabus for chemistry for the JEE MAIN 2014 exam. It covers 27 units of chemistry across three sections - physical chemistry, inorganic chemistry, and organic chemistry. The physical chemistry section covers topics like states of matter, atomic structure, chemical bonding, thermodynamics, solutions, and equilibrium. The inorganic chemistry section discusses periodic properties, metals/alloys, s-block and p-block elements, and coordination compounds. The organic chemistry section addresses purification/characterization, basic principles, hydrocarbons, organic compounds by functional groups (halogens, oxygen, nitrogen), polymers, and biomolecules.
Introduction of Chemistry Syllabus of B. Sc. Part-I (Semester-II) by Dr Pram...pramod padole
Ìý
This document provides an introduction to the B.Sc. Part I Semester II chemistry syllabus from Shri Shivaji Science College in Amravati, India. It outlines the six units that will be covered: inorganic chemistry (units I-II), organic chemistry (units III-IV), and physical chemistry (units V-VI). Each unit is briefly described, including topics like polarisation, covalent bonding, acids and bases (unit I), p-block elements, noble gases, and non-aqueous solvents (unit II). Contact information is provided for questions.
This document provides an outline for teaching organic chemistry. It covers general principles like hybridization and bond properties. It then discusses specific classes of compounds like alkanes, alkenes, alkynes, alcohols, alkyl halides, aldehydes, ketones, carboxylic acids and their derivatives. Protection and deprotection of functional groups is introduced. The document also covers aromaticity, aromatic compounds, heterocyclic compounds, carbohydrates, amino acids, proteins, and pericyclic reactions. Specific reactions involving carbonyl groups are also detailed along with stereochemistry.
Chapter 2 polar covalent bonds acids and basesWong Hsiung
Ìý
This document summarizes key concepts about polar covalent bonds and acid-base chemistry from Chapter 2 of an organic chemistry textbook. It discusses how electronegativity differences between atoms lead to polar covalent bonds and molecular polarity. Bond polarity is quantified using dipole moments. The Brønsted-Lowry definition of acids and bases in terms of proton transfer is introduced. Acid strength is described using acid dissociation constants (Ka) and their pKa values. Factors that influence acid and base strength are also covered.
1) Organic chemistry is the study of carbon compounds and their properties. It is a separate discipline due to the vast number and variety of organic compounds, many of which are essential to life.
2) Carbon can form chains and rings by bonding to itself and other elements like hydrogen, oxygen, nitrogen and halogens. Functional groups like alcohols, aldehydes, ketones and carboxylic acids determine the properties and reactivity of organic molecules.
3) Chiral molecules are non-superimposable mirror images called enantiomers that can have different biological effects. The R/S system is used to distinguish these two forms.
This document outlines the syllabus for chemistry for class 11 in India. It includes:
1. The topics to be covered in terms 1 and 2, such as atomic structure, chemical bonding, redox reactions, and organic chemistry.
2. The number of periods and marks allocated for each topic.
3. Details of the practical exams to be conducted each term, involving volumetric analysis, salt analysis, and other experiments.
4. Guidelines for evaluating visually handicapped students in practical exams by rationalizing the syllabus.
1. The document discusses organic chemistry, which involves the study of carbon-containing compounds. It covers topics such as classification of organic molecules, structural representation, functional groups, and reaction types.
2. Organic compounds are classified as aliphatic, heterocyclic, and homocyclic compounds. Structural formulas are used to represent organic molecules, including complete, condensed, and bond line formulas.
3. Functional groups determine properties of organic compounds. Reaction types covered include substitution, addition, elimination, and rearrangement reactions.
This document discusses inductive effects, resonance, and hyperconjugation. It defines resonance structures as alternative arrangements of electrons that stabilize molecules, and describes how resonance hybrids depict delocalized electrons. It explains that inductive effects stabilize charges through sigma bond polarization from electronegative atoms. Finally, it describes how hyperconjugation delocalizes positive charges in carbocations through overlap of vacant p orbitals with adjacent carbon-hydrogen sigma bonds.
This document provides information about a textbook on organic chemistry. It was published in 2004 as the second edition. The textbook aims to provide comprehensive yet concise basic notes on core topics of organic chemistry for undergraduate students. It focuses on the essential concepts across 15 sections, condensing the material into 310 pages to make it more manageable for students compared to larger textbooks. The goal is for students to understand reaction mechanisms, which brings logic and clarity to remembering reactions of different functional groups.
Chapter 06 an overview of organic reactions Wong Hsiung
Ìý
This document discusses organic reaction mechanisms. It explains that reactions occur through a series of steps, and may involve intermediates that are neither the starting reactants nor final products. Polar reactions involve the combination of electrophiles and nucleophiles, while radical reactions involve the formation and reaction of free radicals. The mechanism of HBr addition to ethylene is used as an example, involving the carbocation intermediate. Reaction steps and intermediates are illustrated using energy diagrams, and factors like bond energies and transition states are also discussed.
COMPREHENSIVE HANDOUT FOR ORGANIC CHEMISTRYPaolo Naguit
Ìý
This document provides an overview of organic chemistry nomenclature and structural formulas. It discusses the different types of structural formulas used to depict organic molecule structures, including straight-line, condensed, 3D, and skeletal formulas. It also outlines the IUPAC rules for systematic nomenclature, including naming conventions for functional groups, prefixes, parents, locants, and suffixes. Key aspects covered include priority rules for determining the parent chain and functional group that occupies the suffix. Functional groups are organized by priority in a table with their corresponding prefixes and suffixes. Naming conventions are also discussed for classes of organic compounds including alkanes, alkyl halides, alkenes and alkynes.
Organic compounds are vital for life and include substances like DNA, proteins, fuels, polymers, dyes, and medicines. Carbon has the unique ability to form covalent bonds with itself and other elements through a process called catenation. The shapes of organic molecules like methane, ethene, and ethyne are determined by the hybridization of carbon - methane is tetrahedral due to sp3 hybridization, ethene is planar due to sp2 hybridization, and ethyne is linear due to sp hybridization. Hybridization also influences bond lengths and energies. π-bonds form through parallel sideways overlap of p-orbitals on adjacent carbons and have electron density above and below the plane of the bonded atoms
The document discusses chirality in heteroatom systems where chirality arises from a non-carbon centre. It explains that compounds containing nitrogen, phosphorus, sulfur or other atoms can exhibit stereochemistry when the atom forms a tetrahedral structure with four different groups. The stereochemistry of these compounds provides useful information for drug applications. It then focuses on the specific stereochemistry of various nitrogen, phosphorus and sulfur compounds, including amines, oximes, azo compounds, phosphines and sulfoxides. It describes how these compounds can exhibit geometrical isomers, inversion barriers, and retention or inversion of configuration under chemical reactions.
The document provides a year-at-a-glance pacing guide for a Chemistry I course. It outlines the major topics to be covered in each of the four nine-week periods, including: introduction to chemistry, matter and energy, the periodic table, chemical bonding and molecular structures in the first period; nomenclature and formulas, chemical reactions, the mole, and stoichiometry in the second period; states of matter, solutions, acids and bases in the third period; and reaction rates, gas laws, nuclear chemistry, energy and chemical change, and an introduction to organic chemistry in the fourth period.
This document provides information about the Organic Chemistry CHEM 230 course. It includes details about the instructor, course objectives, content, textbooks, grading breakdown, and Chapter 1 topics. The key points are:
1. The course is taught by Dr. Suzan Abdulrahman Khiyat and covers the theoretical and experimental basis of organic chemistry for non-chemistry students.
2. Chapter 1 topics include carbon compounds and chemical bonds, isomers, 3D shapes of molecules, electronegativity, and resonance.
3. Student evaluation is based on two midterms, a lab, and a final exam, totaling 100 points.
Optical activity in catenanes and rotaxanesPRUTHVIRAJ K
Ìý
These class of compounds do not contain any formal chiral centre but exhibit stereoisomerism due to presence of either a chiral axis or a chiral plane and are called stereoaxis and stereoplanes respectively
This document provides an outline for topics to be discussed in an organic chemistry tutorial, including: introduction to organic chemistry; nomenclature; carbon properties including hybridization and bonds; isomers and stereochemistry; chirality of molecules including conformational and configurational isomers; and relative and absolute configuration. The tutorial will cover key organic chemistry concepts such as naming organic compounds, identifying isomers, hybridization principles, and the 3D arrangement of atoms in chiral molecules.
The document provides an overview of the chemistry syllabus for JAM 2022, covering both physical chemistry and organic chemistry topics. It includes sections on atomic and molecular structure, the gaseous state, chemical thermodynamics, chemical kinetics, spectroscopy, and inorganic chemistry topics like periodic properties, transition metals, and main group elements. The syllabus also covers organic reaction mechanisms, natural products, aromatic compounds, qualitative organic analysis, and instrumental methods of analysis.
This document provides the syllabus for chemistry for the JEE MAIN 2014 exam. It covers 27 units of chemistry across three sections - physical chemistry, inorganic chemistry, and organic chemistry. The physical chemistry section covers topics like states of matter, atomic structure, chemical bonding, thermodynamics, solutions, and equilibrium. The inorganic chemistry section discusses periodic properties, metals/alloys, s-block and p-block elements, and coordination compounds. The organic chemistry section addresses purification/characterization, basic principles, hydrocarbons, organic compounds by functional groups (halogens, oxygen, nitrogen), polymers, and biomolecules.
This document provides information about a Chemistry course offered at Universiti Teknologi MARA Perlis. The course is for the Diploma in Planting Industrial Management program and is worth 3 credit hours. The course outline covers topics including the structure of atoms and molecules, electronic structure of atoms, the periodic table, chemical bonding, inorganic chemistry, oxidation and reduction, acids and bases, and organic chemistry. Student assessment includes tests, laboratory work, and a final exam worth 60% comprising both objective and subjective questions. The recommended textbook is Essential Chemistry by Raymond Chang.
This document provides an overview of the course curriculum for Physical Chemistry (Hons./PG). It covers 5 units that include topics such as states of matter, thermodynamics, kinetics, nuclear chemistry, and periodicity. Some key areas discussed are van der Waals equation, colligative properties, chemical equilibrium, electrochemistry, atomic structure, radioactivity, and bonding theories (valence bond theory, molecular orbital theory). Experimental techniques like spectrophotometry and analytical methods including pH titration are also mentioned. The document provides detailed sections on the various subtopics that will be covered within each unit of the course.
This document outlines the syllabus for Semesters III and IV of an S.Y.B.Sc. in Chemistry. Semester III covers Physical and Inorganic Chemistry, including topics like thermodynamics, chemical equilibrium, phase equilibrium, and the chemistry of transition metals. Semester IV covers similar topics, along with electrochemistry, solid state, and colloidal chemistry. Both semesters include organic chemistry courses covering topics such as spectroscopy, alcohols, ethers, aldehydes and ketones. The document also lists textbooks, reference books, and laboratory experiments for each semester.
The document discusses the exam pattern and syllabus for the Combined Geo-Scientist Examination conducted by UPSC for the position of Chemist Gr 'A' in the Geological Survey of India. It has three stages - Stage I involves a preliminary exam testing general studies and chemistry knowledge, Stage II involves descriptive exams testing inorganic, physical and analytical chemistry, and Stage III involves a personality test. The document provides details of the exam format, marking schemes, eligibility criteria and syllabus for each exam stage.
The document provides information about a book titled "JEE Main & Advanced IITJEE Solved Papers Chemistry 2021-1979" published by Arihant Prakashan. It includes the publisher information, contents of the book covering 33 chapters on different topics of chemistry, and information about the author Ranjeet Shahi. It also lists the sales and support offices of the publisher across different cities in India.
The document outlines the syllabus for Paper III of the B.Sc. Chemistry program at Dr. B.R. AMBEDKAR University. The syllabus covers inorganic chemistry, organic chemistry, and physical chemistry over 3 units and 90 hours. Some of the main topics included are coordination chemistry, spectral properties of metal complexes, nitrogen compounds, carbohydrates, chemical kinetics, and photochemistry.
The document is a syllabus for the GPAT-2019 exam covering topics in physical chemistry, physical pharmacy, and organic chemistry. Some key topics included are:
1. Physical chemistry topics like thermodynamics, electrochemistry, kinetics, and solutions.
2. Physical pharmacy topics like surface phenomena, rheology, dispersion systems, and solubility.
3. Organic chemistry topics like functional group chemistry, aromatic compounds, carbonyl reactions, heterocyclic chemistry, and stereochemistry.
The syllabus provides an overview of the concepts and reactions to be covered in each topic for the exam.
This document provides the syllabus for the chemistry portion of the National Entrance Screening Test (NEST) for admission to 5-year integrated M.Sc programs in 2021. It lists the topics that will be covered in physical chemistry, inorganic chemistry, and organic chemistry. The physical chemistry section includes topics like thermodynamics, chemical kinetics, and solutions. The inorganic chemistry section covers classification of elements, main group and transition metal chemistry. The organic chemistry section lists topics in basic concepts, reactive intermediates, functional groups, carbohydrates, polymers and more.
1. The document outlines the revised syllabus for Class XII Chemistry for the 2020-21 session.
2. It describes 14 units that will be covered including topics on solid state, solutions, electrochemistry, chemical kinetics, surface chemistry, p-block elements, d-block elements, coordination compounds, haloalkanes and haloarenes, alcohols/phenols/ethers, aldehydes/ketones/carboxylic acids, organic compounds containing nitrogen, and biomolecules.
3. Key concepts from each unit are highlighted such as classification of solids, colligative properties of solutions, redox reactions and EMF of cells in electrochemistry, rate laws and
The document provides a detailed syllabus for the semester 1 course Physical Organic Chemistry, outlining 45 hours of content over topics including molecular orbital theory, kinetics and reaction mechanisms, acid-base catalysis, and charge transfer complexes and reactions. It lists recommended textbooks and includes learning objectives for relating concepts to drug effects on macromolecular targets.
The document provides a detailed syllabus for Physical Organic Chemistry and Physical Pharmacy I courses in the first semester of a B.Pharm program. It includes 45 hours of content over 4 topics for Physical Organic Chemistry, covering modern bonding theories, kinetics, acid-base catalysis, and charge transfer complexes. It also includes 60 hours of content over 5 topics for Physical Pharmacy I, covering states of matter, physical properties of drug molecules, solutions of non-electrolytes, thermodynamics, and properties of electrolyte solutions. The syllabus outlines the specific subtopics to be covered within each topic along with the number of hours to be spent on each subtopic. Recommended textbooks are also provided.
This document outlines the syllabus for a chemistry course. It covers 16 units that include topics such as solid state chemistry, solutions, electrochemistry, chemical kinetics, surface chemistry, isolation of elements, p-block elements, d- and f-block elements, coordination compounds, organic compounds, biomolecules, and polymers. The course will conclude with a unit on chemicals used in everyday life such as medicines, food, and cleaning agents. Students will take one exam consisting of 25 compulsory questions to assess their understanding of the material covered over the semester.
This document provides the syllabus for the examination for the post of Senior Teacher (Grade-II) in the Secondary Education Department of Rajasthan Public Service Commission.
It outlines the topics to be covered in Paper II - Science, which is divided into two parts. Part I covers topics in biology, chemistry, and physics at the secondary and senior secondary level. Part II covers more advanced topics in biology, chemistry, and physics at the graduate level.
The syllabus provides detailed lists of concepts and topics to be studied within each subject for the examination, with approximately 180 marks allotted to questions from Part I and 80 marks from Part II.
CBSE Deleted Syllabus Class 11, 12 Chemistry 2020-21Anand Meena
Ìý
The document discusses proposed reductions to the CBSE Board syllabus for Chemistry for classes 11 and 12.
For class 11, some topics proposed for reduction include laws of chemical combination under basic concepts, classification of elements and periodicity in properties, states of matter, and chemical thermodynamics. For the practical portion, experiments involving pH determination and chemical equilibrium are proposed to be reduced.
For class 12, some topics proposed for reduction include electrical and magnetic properties in solids, abnormal molecular mass in solutions, lead accumulator and dry cells in electrochemistry, and collision theory in chemical kinetics. Portions of several other units are also proposed for reduction, and some practical experiments are proposed to be removed.
CBSE Deleted Syllabus Class 11, 12 Chemistry 2020-21Anand Meena
Ìý
F.Y. B.Sc.
1. 1
F. Y. B. Sc CHEMISTRY SYLLABUS
SEMESTER – I: COURSES CH – 101 AND CH – 103
SEMESTER – II: COURSES CH – 102 AND CH - 104
SEMESTER – I
CH-101 : Physical & Inorganic Chemistry
Section - I (Physical Chemistry)
I Mathematical Concepts 06 L
Logarithmic relations, curve sketching, linear graphs and calculations of slopes
differentiation of functions like Kx, ex
, xn
, sin x, log x, maxima & minima, partial,
differentiation & reciprocity relations. Integration of some useful/relevant functions
II Gaseous State 10 L
Postulates of kinetic theory of gases and deviation from ideal behaviour, Van der Waal’s
equation of state.
Critical phenomena; PV isotherms of real gases, continuity of states , the isotherms of
van der Waal’s equation, relationship between critical constants and van der Waal’s
constants , the law of corresponding states, reduced equation of state.
Molecular Velocities: Root mean square, average and most probable velocities.
Qualitative discussion of the Maxwell’s distribution of molecular velocities, collision
number, mean free path and collision diameter, liquifacation of gases (based on Joule –
Thomson effect)
III Chemical Kinetics 14 L
Rate of reaction, factors influencing the rate of a reaction concentration, temperature,
pressure, solvent, light, catalyst Concentration dependence of rates mathematical
characteristics of simple chemical reaction. Zero order, first order, second order, pseudo
order, half life & mean life. Determination of order of reaction: Differential method
Integration method, Method of half life period & Isolation method.
Radioactive decay as a first order phenomenon.
Theories of Chemical Kinetics. Effect of temperature on the rate of reaction, Arrhenius
equation and concept of activation energy. Simple collision theory based on hard sphere
model. Transition state theory (equilibrium hypothesis ). Expression for the rate constant
based on equilibrium constant & thermodynamic aspects.
Section – II (Inorganic Chemistry)
I. Atomic Structure 06 L
Evidence for the electrical nature of matter; discharge tube experiments; Thomson’s
atomic model; Rutherford model; Bohr's model of hydrogen atom; probability picture of
electron; quantum numbers; Shapes of s, p, d, orbitals; Aufbau and Pauli exclusion
principles, Hund’s rule of maximum multiplicity; Electronic configurations of the
elements; effective nuclear charge.
2. 2
.
II. Chemical Bonding (A) 09 L
Covalent bond – Valence Bond Theory (VBT) and its limitations, directional
characteristics of covalent bond, various types of hybridization and shapes of simple
inorganic molecules and ions. Valence Shell Electron Pair Repulsion Theory (VSEPR
Theory) to NH3, H3O+
, SF4, ClF3, ICl2
-
and H2O. Molecular Orbital Theory,
homonuclear and heteronuclear diatomic molecules(CO and NO), multicenter bonding in
electron deficient molecules, bond strength and bond energy, percentage ionic character
from dipole moment and electronegativity difference.
Text Books
1 P.W. Atkins et al., Physical Chemistry, 7th
edition
2. J.D. Lee, Concise Inorganic Chemistry, ELBS publications, 4th
edition
Reference Books
Physical Chemistry
1. Puri, Sharma, Pathania,Principles of Physical Chemistry by
Vishal Publishing Company, Oxford University Press
2. G. K. Vemulapalli, Physical chemistry, Prentice Hall India, 1993,
3. Donald McQuarrie, Physical Chemistry
4. G. L. Agarwal, Basic Chemical Kinetics, Tata McGraw-Hill Publication
Inorganic Chemistry
1. B.R. Puri, L.R.Sharma, K.C. Kale, Principles of Inorganic Chemistry
Vallabh Publications, First Edition
2. F.A. Cotton and G.Wilkinson Basic Inorganic Chemistry,
Wiley Eastern Ltd, 2nd
edition,1993
3. C N R Rao,University General Chemistry , Mc Millan , 1993.
4. Sharpe and Emilus, Inorganic Chemistry , , ELBS publications.New edition
5. N.N. Greenwood and Earnshaw, Chemistry of Elements, , Pergamon, Oxford,1984.
CH-103 :Organic& Inorganic Chemistry
Section – I (Organic Chemistry)
I. Structure and Bonding: 4 L
Hybridization, C-C bond lengths and bond angles, bond energy, localized and
delocalized chemical bonds, Definition and examples of Van der Waals interactions,
resonance, hyperconjugation, inductive and field effects, intramolecular and
intermolecular hydrogen bonding.
II. Fundamentals of Organic Chemistry: 8 L
Curved arrow notation, drawing electron movement with arrows, half and double
headed arrows, homolytic and heterolytic bond breaking. Types of reagents –
3. 3
electrophiles and nucleophiles with examples. Types of Organic Reactions: Addition,
Elimination, Substitution, Oxidation, Reduction and Rearrangement-one example of
each. Energy profile diagrams for exothermic and endothermic reactions, single step
and two step reactions. Reactive intermediates – Carbocations, carbanions, free
radicals, carbenes, arynes and nitrenes; examples, shape and ways of formation.
Assigning formal charges on intermediates and other ionic species. Methods of
determination of reaction mechanisms (one example each of product analysis,
intermediates, isotope effects, kinetic and stereochemical studies).
Theory of acids and bases: Lewis concept; Bronsted and Lowry concept
III. Alkanes and cycloalkanes: 6 L
IUPAC nomenclature of alkanes. General methods of formation (with special
reference to Wurtz reaction, Kolbe reaction, Corey-House reaction &
decarboxylation of carboxylic acids). Physical properties and chemical reactions of
alkanes: halogenation, combustion and pyrolysis. Mechanism of free radical
halogenation of alkanes: orientation, reactivity and selectivity with propane as an
example. Cycloalkanes – nomenclature, general methods of formation, Baeyer strain
theory and its limitations. Ring strain in small rings (cyclopropane and cyclobutane),
theory of strainless rings. The case of cyclopropane ring: banana bonds.
IV. Alkenes, dienes and alkynes: 12 L
IUPAC nomenclature of alkenes, general methods of formation, mechanisms of
dehydration of alcohols and dehydrohalogenation of alkyl halides, regioselectivity in
alcohol dehydration. The Saytzeff rule, Hoffmann elimination, physical properties
and relative stabilities of alkenes.
Chemical reactions of alkenes – Epoxidation, ozonolysis, hydration, hydroxylation
and oxidation with KMnO4. Mechanisms involved in hydrogenation, electrophilic
and free radical additions, Markownikoff’s rule, hydroboration-oxidation,
oxymercuration-reduction. Polymerization of alkenes. Substitution at the allylic and
vinylic positions of alkenes. Industrial applications of ethene and propene.
Nomenclature and classification of dienes, isolated, conjugated and cumulated dienes.
Structure and stereochemistry of allenes, methods of formation of butadiene,
polymerization. Chemical reactions – 1,2- and 1,4-additions, Diels-Alder reaction.
Nomenclature, structure and bonding in alkynes. General methods of formation.
Chemical reactions of alkynes, acidity of alkynes. Mechanism of electrophilic and
nucleophilic addition reactions, metal-ammonia reduction and polymerization.
Section – II (Inorganic Chemistry)
I. Periodic Properties 05 L
Atomic and ionic radii, ionization energy, electron affinity and electronegativity,
definition, methods of determination or evaluation, trends in periodic table and
applications in predicting and explaining the chemical behaviour.
II. Acids, Bases and Non Aqueous Solvents 10 L
Arrhenius Concept and Bronsted Theory. The Lux – Flood Solvent Systems.
4. 4
Lewis Concept of Acids and Bases.
Physical Properties of a solvent. Types of Solvents and their general Characteristics.
Reactions in non aqueous solvents with respect to liquid NH3 and liquid SO2.
Text Books
1. Morrison and Boyd, Organic Chemistry;; 6th Edition, Prentice Hall India
2. J.D. Lee, Concise Inorganic Chemistry, ELBS publications, 4th
edition
Reference Books
Organic Chemistry
1. Francis Carey, Organic Chemistry; 3rd
Edition, Tata McGraw Hill India
2. Paula Yurkanis Bruice, Organic Chemistry; 3rd
Edition, Pearson Education Asia
3. Jerry March, Advanced Organic Chemistry; 4rd
Edition, John Wiley
Inorganic Chemistry
1. B.R. Puri, L.R.Sharma, K.C. Kale, Principles of Inorganic Chemistry
Vallabh Publications, First Edition
2. F.A. Cotton and G.Wilkinson Basic Inorganic Chemistry,
Wiley Eastern Ltd, 2nd
edition,1993
3. C N R Rao,University General Chemistry , Mc Millan , 1993.
4. Sharpe and Emilus, Inorganic Chemistry , , ELBS publications.New edition
5. N.N. Greenwood and Earnshaw, Chemistry of Elements, , Pergamon, Oxford,1984.
Laboratory Course for the entire semester i.e. for courses CH – 101 and CH 103:
PHYSICAL CHEMISTRY
Chemical Kinetics :
1. Hydrolysis of Methyl Acetate using two different initial concentrations in presence
of mineral acid (HCl) as catalyst.
2. Relative strength of two acids i.e. HCl & H2SO4.
3. Degree of hydrolysis of urea hydrochloride.
4. Measurements of viscosity of a given liquid using Ostwald’s viscometer
(minimum three liquids)
INORGANIC CHEMISTRY
Calibrations and dilutions:
1. Calibration of Burette and Pipettes.
2. To prepare 100 mL of standard 0.1 M K2Cr2O7 solution and carry out dilution to
0.05, 0.01, 0.005, and 0.001 M in 100 mL standard flasks.
3. To prepare 100 ppm of Manganese solution using KMnO4 and carry out dilution
of 5, 10, 15, 20 and 25 mL in 100 mL standard flasks.
5. 5
4. Semi-micro qualitative analysis:
To analyse 4 - 6 inorganic mixtures containing four ions only.(Two cations and two
anions). Mixtures containing the following ions may be prepared
Cations :
Pb2+
, Bi3+
,Cu2+
, Cd2+
, Sn2+
, Sb3+
,Fe2+
, Fe3+
, Al3+
,Cr3+
,Zn2+
, Mn2+
, Ni2+
, Co2+
,
Ba2+
, Sr2+
,Ca2+
, Mg2+
, (NH4) +
, K+
Anions:
Cl¯, Br¯, I¯, NO2¯, NO3¯, SO3
2¯
, CO3
2¯
, SO4
2¯
, CrO4
2¯
, PO4
3¯
.
ORGANIC CHEMISTRY
I. Crystallization: - a) Benzoic acid from hot water. b) m-dinitrobenzene from ethanol
II. Sublimations: - a) Naphthalene and b) Anthracene
III.Distillation: - a) Separation of acetone and ethyl acetate using water condenser.
b) Separation of toluene and nitrobenzene using air condenser.
IV. Qualitative Analysis:
List of compounds
Acids: Benzoic, Acetylsalicylic, Salicylic, Phthalic.
Phenols: Phenol, α-Naphthol, β-Naphthol.
Bases: p-Toluidine, Diphenylamine, o-, m- and p-Nitroanilines, Aniline.
Hydrocarbons: Naphthalene, Anthracene.
Amides: Benzamide, Urea.
Carbonyl compounds: Benzaldehyde, Acetone, Butanone.
Note:
A] 7 compounds of the following types should be analyzed.
Acids – 2; Phenols – 1; Bases – 1; Hydrocarbons – 1; Amide – 1; Carbonyl compds – 1
Tests to be performed are i. Preliminary Tests; ii. Solubility and Chemical type;
iii. Elements; iv. Groups and v. Physical Constant.
B] Qualitative analysis is to be performed at a small scale level using preferably not more
than 1.0 g. solid and 1.0 ml. liquid.
C] The 7 compounds to be completed in 5 practical, while (I-III) to be completed in two
practical.
D]The experiments on distillation/sublimation/crystallization as the case may be are not
to be given for examination. However they are not demonstration experiments.
Every student is expected to perform these experiments.)
Books suggested for laboratory course
1.Vogel’s Qualitative Inorganic Analysis, (revised) Svehla, Orient L:ongman.
2. Vogel’s textbook of Quantitative Inorganic analysis (revised) J. Basset, R.C.
3. Mann and Saunders , Practical Organic Chemistry
4. N.K. Vishnoi, Practical Organic Chemistry
5. P. S. Sindhu, Practicals in Physical Chemistry, Macmillan India Ltd.,
First Edition, 2006.
6. 6
SEMESTER – II
CH-102 : Physical & Inorganic Chemistry
Section - I (Physical Chemistry)
I Thermodynamics 10 L
Thermodynamic terms:System, surrounding, types of systems, intensive & extensive
properties. State & path functions & their differentials. Thermodynamic process.
Concept of work & heat
First law of thermodynamics : statements and definitions of internal energy & enthalpy.
Heat capacities at constant volume & pressure & their relationship. Joule’s law, Joule-
Thomson coefficient & inversion temperature . Calculation of w, q, dU, dH, for the
expansion of ideal gases under isothermal & adiabatic conditions for reversible
processes. Thermochemistry : standard state, standard enthalpy of formation . Hess’s law
of heat summation & its applications. Heat of reaction at constant pressure & at
constant volume . Enthalpy of neutralization, bond dissociation energy & its calculation
from thermochemical data. Temperature dependence of enthalpy. Kirchoff’s equation.
II Solutions, Dilute Solutions and Colligative Properties 10 L
Ideal & non ideal solutions, methods of expressing concentrations of solutions, activity &
activity coefficients.
Dilute solutions, colligatve properties, Roult’s law , relative lowering of vapour pressure
molecular weight determination. Osmosis: osmotic pressure & its measurement,
depression of freezing point, thermodynamic derivation of relation between molecular
weight and depression of freezing point. Elevation in boiling point thermodynamic
derivation of relation between molecular weight and elevation in boiling point.
Experimental methods for determining various colligative properties.
III Liquid State and Applications 10 L
Intermolecular forces, structure of liquids (Qualitative description) Structural differences
between solids, liquids and gases.
Liquid crystal : Difference between liquid crystals ,solid and liquid. Classification,
structure of nematic and cholestric phases. Thermography and seven segment cell.
Surface between a liquid and vapour .Surface tension by capillary rise method,
stalagmometer method .Viscosity of liquids, Poiseuille equation, use of Ostwald’s
Viscometer.
Section – II (Inorganic Chemistry)
I. s – block elements 06 L
Comparative study including diagonal relationship of groups, salient features of
7. 7
Hydrides, solvation and complexation tendencies including their function in biosystems.
An introduction to alkyls and aryls.
II. p - block elements (A) 09 L
Comparative study including diagonal relationship of groups 13 and 14.
Group 13--- Hydrides of Boron, diborane, and higher boranes, borazine, borohydrides.
Group 14 ---Fullerenes, carbides, fluorocarbons, silicates (structural principle)
Text Books :
1. P.W. Atkins et al., Physical Chemistry, 7th
edition
2. J.D. Lee, Concise Inorganic Chemistry, ELBS publications, 4th
edition
Reference Books
Physical Chemistry
1. Puri, Sharma, Pathania,Principles of Physical Chemistry by
Vishal Publishing Company, Oxford University Press
2. G. K. Vemulapalli, Physical chemistry, Prentice Hall India, 1993,
3. Donald McQuarrie, Physical Chemistry
4. G. L. Agarwal, Basic Chemical Kinetics, Tata McGraw-Hill Publication
Inorganic Chemistry
1. B.R. Puri, L.R.Sharma, K.C. Kale, Principles of Inorganic Chemistry
Vallabh Publications, First Edition
2. F.A. Cotton and G.Wilkinson Basic Inorganic Chemistry,
Wiley Eastern Ltd, 2nd
edition,1993
3. C N R Rao,University General Chemistry , Mc Millan , 1993.
4. Sharpe and Emilus, Inorganic Chemistry , , ELBS publications.New edition
5. N.N. Greenwood and Earnshaw, Chemistry of Elements, , Pergamon, Oxford,1984
CH-104 :Organic& Inorganic Chemistry
Section – I (Organic Chemistry)
I. Stereochemistry of organic compounds: 14 L
Newman and saw horse formulae, Fischer and flying wedge formulae.
Concept of isomerism. Types of isomerism. Conformational isomerism –
Conformational analysis of ethane and n-butane; conformations of cyclohexane,
axial and equatorial bonds, conformation of mono-substituted cyclohexane
derivatives.
Optical isomerism – elements of symmetry, molecular chirality, definition and
examples of enantiomers, stereogenic centre, optical activity, properties of
enantiomers, chiral and achiral molecules with two stereogenic centers,
diastereomers, threo and erythro diastereomers, meso compounds, resolution of
enantiomers, inversion, retention and racemization. Specification of configuration at
chiral centers: Sequence rules and R:S system of nomenclature.
Geometric Isomerism - Determination of configuration of geometric isomers.
8. 8
E and Z system of nomenclature, geometric isomerism in oximes and alicyclic
compounds.
Difference between configuration and conformation.
II. Arenes and Aromaticity 09 L
Nomenclature of benzene derivatives. Structure of benzene: molecular formula and
Kekule structure. Stability and C–C bond lengths of benzene, resonance structure,
MO picture. Aromaticity: The Huckel’s rule, aromatic ions, anti-aromaticity.
Aromatic electrophilic substitution – general pattern of the mechanism role of σ- and
Ï€- complexes. Mechanism of nitration, halogenation, sulphonation and Friedel-Crafts
reaction. Activating and deactivating substituents, orientation and ortho/para ratio.
Side chain reactions of benzene derivatives. Birch reduction. General methods of
formation and chemical reactions of alkyl benzenes – reduction, oxidation, ring and
side chain substitution.
III. Alkyl and aryl halides: 07 L
Nomenclature and classes of alkyl halides, general methods of formation, chemical
reactions. Mechanism and stereochemistry of nucleophilic substitution reactions of
alkyl halides, SN2 and SN1 reactions with energy profile diagrams, solvent effect.
The addition – elimination (bimolecular displacement) and the elimination –
addition (benzyne) mechanisms of nucleophilic aromatic substitution reactions.
Relative reactivities of alkyl halides vs. allyl, vinyl and aryl halides.
Section – II(Inorganic Chemistry)
I. p - block elements (B) 12 L
Comparative study including diagonal relationship of groups 15, 16 and 17.
group 15- phosphazenes, group 16—tetra sulfur tetranitride,
group 17—basic properties of halogens, interhalogens and polyhalides.
II. Chemistry of Noble Gases 03 L
Chemical properties of Noble Gases, Chemistry of Xenon, structure and bonding in
Xenon compounds,
Text Books
1. Morrison and Boyd, Organic Chemistry;; 6th Edition, Prentice Hall India
2. J.D. Lee, Concise Inorganic Chemistry, ELBS publications, 4th
edition
Reference Books
Organic Chemistry
1. Francis Carey, Organic Chemistry; 3rd
Edition, Tata McGraw Hill India
2. Paula Yurkanis Bruice, Organic Chemistry; 3rd
Edition, Pearson Education Asia
3. Jerry March, Advanced Organic Chemistry; 3rd
Edition, John Wiley
Inorganic Chemistry
1. B.R. Puri, L.R.Sharma, K.C. Kale, Principles of Inorganic Chemistry
Vallabh Publications, First Edition
9. 9
2. F.A. Cotton and G.Wilkinson Basic Inorganic Chemistry,
Wiley Eastern Ltd, 2nd
edition,1993
3. C N R Rao,University General Chemistry , Mc Millan , 1993.
4. Sharpe and Emilus, Inorganic Chemistry , , ELBS publications.New edition
Laboratory Course for the entire semester i.e for courses 102 and 104:
PHYSICAL CHEMISTRY
1. Measurements of surface tension of a given liquid using
stalagmometer (minimum three liquids)
2. Preparation of standard solutions based on normality,
molarity, molality. Also further dilutions from a standard
solution are expected (e.g. KMnO4, NaOH etc.)
3. Preparation of standard solutions based on ppm and mole
fraction. Also further dilutions from a standard ppm solution
are expected(e.g. Oxalic acid, CuSO4)
4. To investigate the order of the reaction between K2S2O8 + KI
(a = b)
INORGANIC CHEMISTRY
Volumetry: (Double Burette*)
1. To prepare 0.1 N Na2CO3/ Borax solution and standardize the given ≈ 0.1 N HCl
solution.
2. To prepare 0.1 N Succinic acid/KHP solution and standardize the given ≈ 0.1 N
NaOH solution.
Volumetry: (Single Burette)
1. To prepare 0.05 N Na2C2O4 solution and standardize the given KMnO4 solution.
2. To prepare 0.005 M EDTA solution and estimate the amount of Zn2+
and Mg2+
from
ZnSO4.7H2O and MgSO4. 6H2O solutions respectively.
Gravimetric analysis:
1. NH4Cl + BaSO4
2. ZnO + ZnCO3
* Note: The prepared solution in burette no. 1to be titrated with given solution in burette
no. 2 with indicator added once for the first titration, without throwing out the conical
flask content. Plot the readings from burette no. 1 v/s readings from burette no. 2 and
from the graph, calculate the normality of solution in burette no. 2.
ORGANIC CHEMISTRY
1. Qualitative Analysis
10. 10
List of compounds
Alkyl and aryl halides: Chloroform, Carbon tetrachloride, Chlorobenzene,
Bromobenzene, p-dichlorobenzene.
Nitrohydrocarbons: Nitrobenzene, m-dinitrobenzene, p-nitrotoluene.
Bases: α-Naphthylamine, Diphenylamine, o-, m- and p-Nitroanilines,
N-methylaniline, N,N-dimethylaniline.
Alcohols: Methanol, Ethanol, 2-propanol, Cyclohexanol.
Esters: Methyl acetate, Ethyl acetate, Ethyl benzoate, Methyl salicylate.
Anilides: Acetanilide, Benzanilide
Carbohydrates: Glucose, Fructose, Mannose
Note: 7 compounds of the following type to be analyzed in 5 practicals: Carbohydrate –
1; Anilide – 1; Ester – 1; Alcohol – 1; Nitrohydrocarbon -1; Alkyl or aryl halide – 1;
Base – 1.
Books suggested for laboratory course
1. Vogel’s Qualitative Inorganic Analysis, (revised) Svehla, Orient L:ongman.
2. Mann and Saunders , Practical Organic Chemistry
3. N.K. Vishnoi, Practical Organic Chemistry
4. Vogel’s textbook of Quantitative Inorganic analysis (revised) J. Basset, R.C.
5. P. S. Sindhu, Practicals in Physical Chemistry, Macmillan India Ltd.,
First Edition, 2006.