IUPAC Nomenclature and STRUCTURAL ISOMERISM and GENERAL ORGANIC CHEMISTRY GOC
Subject chemistry Medium ENGLISH
Faculty VKP Sir Status AVAILABLE
Category TOPIC BASED COURSE Lecture 31
Target XI XII XIII Books QUESTION BANK ATTACHED
You May Pay in Installments through Credit Card
Product Type Prices Validity
  USB 4300 30%OFF 3010 1 year
Syllabus

IUPAC Nomenclature

Basic organic chemistry, Definition of organic compound , Representation of organic compound , Hybridisation      
Number of Sigma and PI  bonds , Degree of carbon , Degree of hydrogen , Degree of Alkyl halides, Degree of Alcohols ,  Degree of Amines , Degree of unsaturation (DU) , Calculation of DU , Fundamental definition of DU, Homologous series (H.S.)     
Classification of organic compound , Aromatic compounds , Homocyclic compounds , Heterocyclic compounds , IUPAC- Nomenclature , Scheme of IUPAC, Naming of Alkanes
Scheme of IUPAC, Naming of alkanes , Retained Names , Naming of alkenes
Naming of Alkene, Naming of Alkynes , Naming of cycloalkanes
Naming of cycloalkenes , Alkylidenes , Naming of cycloalkynes , Naming of Bicyclo compounds
Functional Groups (F.G.), Naming of carboxylic acids, Special Name of carboxylic acids , Naming of dicarboxylic acids
Naming of sulphonic acid , Naming of Alcohols , Naming of Amines , Naming of thioalcohols, Naming of Aldehydes , Special name of Aldehydes
Naming of Ketones , Naming of cyanides , Special name of cyanides , Naming of isocyanides , Naming of Amides , Special name of amides , Naming of acid halides

naming of acid halide, naming of acid anhydride, naming of esters, special name of ester    
Naming of haloalkanes , Naming of Nitro compounds , Naming of Nitroso compounds , Naming of Aromatic compound , Benzene , Other aromatic compound

STRUCTURAL ISOMERISM

Definition of isomerism, Classification of isomerism, Chain isomerism, Positional isomerism
Functional isomerism, Ring-chain isomerism,  Metamerism

GENERAL ORGANIC CHEMISTRY GOC

Electornic effect , Inductive effect
Applications of  I-Effect  , Resonance , Conjugated system  
When double bond is in conjugation with vacant -p , When double bond is in conjugation with fully filled -p
When double bond is in conjugation with fully filled -p, When double bond is in conjugation with half filled-p ,

When +ve charge and lone pair are adjacent , d-orbital resonance , Conditions of Resonance, Mesomeric effect (M)
Stability of resonating structures (R.S), Steric Inhibition of Resonance (SIR) , Equivalent R.S.
Equivalent R.S. , Hyperconjugation HC , Hyperconjugation in carbocations , Hyperconjugation in Alkenes , Heat of hydrogenation (HOH)
Hyperconjugation in Toluene, Hyperconjugation in Free Radicals, Electromeric effect (E), Applications of electronic effects , Dipole moment, Bond length , Aromaticity , Benzenoids and Non-benzenoids
Examples of aromatic compounds , Heterocyclic aromatic compounds
M.O. Diagram, Polycyclic aromatic compounds
Examples of aromatic  systems, [n] Annulenes , NMR- definition of Aromaticity , Resonance energy (RE)
Acidic strength of acids , Acidic strength of dicarboxylic acids
Aromatic acids , Ortho effect, Acidic strength of phenols , Feasibility of reactions , Sodium bicarbonate test of acids
Basic strength , Organic Nitrogenous bases.     
Basic strngth of Aliphatiec amines , Aromatic amines
Basic strength of Amidines , Basic strength of Guanidines,  Proton sponges,  Site of protonation , Feasibility of Reaction
Carbanions (C-), Reactions in which carbanions are formed , Organometallic compounds, Active methylene group., Tautomerism, Types of Tautomerism
Enolisable –H, Keto-enol Tautomerism, Mechanism of keto-enol Tautomerism     
Stability of enol (Percentage enol-content), Racemisation due to enolisation     
D-Excharge , Tautomerism in phenols , Ring-chain Tautomerism , Unsymmetrical alpha-hydroxy ketones

 

Write Your Review