Sections in the chapter
14.1 Tetravalency of Carbon
14.2 Hybridization and Shapes of Molecules
14.3 Structural Representation of Organic Compounds
14.4 Functional Group
14.5 Homologous Series
14.6 Different Classes of Aliphatic Compounds and Their Nomenclature
14.7 General Rules for Naming Organic Compounds
14.8 Writing Structural Formula from the Name of the Compound
14.9 Nomenclature of Aromatic Compounds
14.10 Isomerism
14.11 Electron Displacement in Covalent Bonds
14.12 Types of Bond Fission
14.13 Types of Attacking Reagents
14.14 Types of Organic Reactions
Conceptual Questions with Answers: 18
Additional Numerical Problems for Practice:
Revision Exercises
Very Short Answer questions 40
Short Answer Questions 40
Long Answer Questions 14
Competition File
Numerical Problems
Objective Questions: 40
Fill in the blanks: 10
True or False: 10
Study Plan
Day 1
14.1 Tetravalency of Carbon
14.2 Hybridization and Shapes of Molecules
Ex. 14.1, 14.2
Practice Problems 14.1 to 4
Day 2
14.3 Structural Representation of Organic Compounds
Ex. 14.3 to 6
14.4 Functional Group
14.5 Homologous Series
Day 3
PP. 14.5 to 14.8
14.6 Different Classes of Aliphatic Compounds and Their Nomenclature
1. Hydrocarbons and 2 alkyl halides
Day 4
14.6 contd. 3 and 4
14.7 General Rules for Naming Organic Compounds
Day 5
14.7 contd.
Day 6
14.8 Writing Structural Formula from the Name of the Compound
14.9 Nomenclature of Aromatic Compounds
Day 7
Nomenclature Revision
Day 8
14.10 Isomerism
Day 9
14.11 Electron Displacement in Covalent Bonds
Day 10
14.12 Types of Bond Fission
14.13 Types of Attacking Reagents
Day 11
14.14 Types of Organic Reactions
Day 12
Conceptual Questions 1 to 18
Revision Exercises:Very Short Answer questions 1 to 30
Day 13
Revision Exercises:Very Short Answer questions 31 to 40
Revision Exercises: Short Answer Questions 1 to 40
Day 14
Competition File: Objective Questions: 40
Day 15
Competition File: Fill in the blanks: 10
Competition File: True or False: 10
Revision Period
Days 16 to 30
Revision and test paper problems solving
The blog mainly contains Study guides for various topics in JEE Syllabus and Revision material of Chemistry. Model questions and Practice Questions are provided in separate blogs.
Showing posts with label Gen-org-chemistry. Show all posts
Showing posts with label Gen-org-chemistry. Show all posts
Wednesday, March 11, 2009
Sunday, December 28, 2008
Organic Chemistry Concepts - General Organic Chemistry - - Study Guide - IIT JEE
Hybridisation of carbon; Sigma and pi-bonds; Shapes of molecules;
Structural and geometrical isomerism; Optical isomerism of compounds containing up to two asymmetric centers, (R,S and E,Z nomenclature excluded);
Conformations of ethane and butane (Newman projections);
IUPAC nomenclature of simple organic compounds (only hydrocarbons, mono-functional and bi-functional compounds);
Resonance and hyperconjugation; Keto-enol tautomerism;
Determination of empirical and molecular formula of simple compounds (only combustion method);
Hydrogen bonds: definition and their effects on physical properties of alcohols and carboxylic acids;
Inductive and resonance effects on acidity and basicity of organic acids and bases;
Polarity and inductive effects in alkyl halides;
Reactive intermediates produced during homolytic and heterolytic bond cleavage; Formation, structure and stability of carbocations, carbanions and free radicals.
Structural and geometrical isomerism; Optical isomerism of compounds containing up to two asymmetric centers, (R,S and E,Z nomenclature excluded);
Conformations of ethane and butane (Newman projections);
IUPAC nomenclature of simple organic compounds (only hydrocarbons, mono-functional and bi-functional compounds);
Resonance and hyperconjugation; Keto-enol tautomerism;
Determination of empirical and molecular formula of simple compounds (only combustion method);
Hydrogen bonds: definition and their effects on physical properties of alcohols and carboxylic acids;
Inductive and resonance effects on acidity and basicity of organic acids and bases;
Polarity and inductive effects in alkyl halides;
Reactive intermediates produced during homolytic and heterolytic bond cleavage; Formation, structure and stability of carbocations, carbanions and free radicals.
Wednesday, December 24, 2008
General Organic Chemistry
The chapters that deal with concepts applicable to all the organic compounds may be grouped under the head General Organic Chemistry. Six posts follow this chapter to cover various concepts applicable to all the compounds. All the posts are revision points only. The detailed reading of the material has to be done from the text books.
Concept of Acids and Bases - Application to Organic Compounds
Bronsted-Lowry theory
Acid is a proton donor and based is proton acceptor.
Any compound that has a hydrogen atom can act as a Bronsted-Lowry acid.
Hence H-A is used as general representation for an acid (H represents hydrogen)
Lewis Theory
According to Lewis theory, any molecule that has an electron deficient atom (site) that can accept a pair of electrons, is an acid.
Conjugate acid
Conjugate base
Acidity constant
Ph value
The effects of structure of the molecule on the strengths of acids and bases
Acids and Bases - Videos on Knol
Acid is a proton donor and based is proton acceptor.
Any compound that has a hydrogen atom can act as a Bronsted-Lowry acid.
Hence H-A is used as general representation for an acid (H represents hydrogen)
Lewis Theory
According to Lewis theory, any molecule that has an electron deficient atom (site) that can accept a pair of electrons, is an acid.
Conjugate acid
Conjugate base
Acidity constant
Ph value
The effects of structure of the molecule on the strengths of acids and bases
Acids and Bases - Videos on Knol
Bonding Concepts - Organic Compounds
Valency
Electronegativity
polarity
Dipole momennt
Atomic orbitals
Molecular orbitals
Hybridisation
Resonance
Electronegativity
polarity
Dipole momennt
Atomic orbitals
Molecular orbitals
Hybridisation
Resonance
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