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CHem 2
CHem 2
General Principles and Processes of Isolation of Elements Chemistry in Everyday Life Environmental Chemistry
▪ Occurrence of Metals ▪ Medicines ▪ Pollution -S N CO2 CO Hydrocarbon Gases
▪ Concentration of Ores –Hydraulic Washing, Magnetic ▪ Drugs -Antacid, Tranquilizer, Noradrenaline -Global warming Gree house effect
Separation -Froth Floatation, Leaching -Barbituric acid, Analgesic(narcotic, Non-Narcotic -Particulate- Smoke Dust Mist Fume
▪ Metal Crude Extraction -Oxide Conversion (Calcination: Roasting) -Antimicrobial, Antipyretics, Antibiotics ,penicillin -Petrochemical smog
-Oxide Reduction -Antiseptics, Disinfectants -ozone Hole &depletion
▪ Thermodynamic Principles of Metallurgy & Blast furnace ▪ Drug-Target Interaction ▪ Water Pollution -Pathogen Organic waste
▪ Electrochemical Principles of Metallurgy & Aluminum, Copper ▪ Therapeutic Action of Different Classes of Drugs -Chemical Pollutant
▪ Oxidation Reduction ▪ Chemicals in Food -Artificial sweetening, Saccharin Cyclamate -Biochemical oxygen Demand
▪ Refining -Distillation Liquation Electrolysis Zone refining -Aspartame, Alitame, Sucralose ▪ Water Standard
-Vapor phase refining (Mond van Arkel) Chromatography ▪ Food Preservatives-Sodium benzoate
▪ Uses of Aluminium, Copper, Zinc and Iron -Antioxidants (butylated-hydroxyaniline/toluene) ▪ Soil Pollution – (Pesticide Industrial waste)
▪ Cleansing Agents –Preparation of Soaps ▪ Environmental Pollution control
-Anionic Cationic Non-ionic Detergent ▪ Green Chemistry (Dry cleaning, Paper Bleaching, Ethanol)
Surface Chemistry 5 ▪ Dye (Vat Direct Acid Bases Ingrain Mordant)
▪ Absorption & Adsorption(physisorption & chemisorption) Types- Anthraquinone Phthalein Triarybnethane Indigo Nitroso Azo
▪ Catalysis (heterogenous homogenous enzymes) ▪ Cosmetics(Cream Perfume Talcum Powder Deodorant
▪ Colloids & Classification of Colloids ▪ Rocket Propellent & Solid Propellant
▪ Emulsions
Polymers
▪ Polymers -Natural Synthetic Semi-Synthetic
-Linear Branched Network
-Addition & Condensation
-Elastomer Thermoplastics Thermosetting Fiber
▪ Condensation & Addition Polymerization
▪ Molecular Mass of Polymers
▪ Rubber (Vulcanization)
▪ Biodegradable & Non-Biodegradable Polymers
▪ Nylon Neoprene Bakelite Polypropylene Polystyrene PET PTFE PVC
Hydrogen Organic Chemistry – Some Basic Principles & Techniques Hydrocarbons Haloalkanes and Haloarenes
▪ Dihydrogen (Occurrence & Isotopes) ▪ Carbon Tetravalence (Organic Compounds Shapes , Pi bond) ▪ Alkanes -Nomenclature & isomerism ▪ Classification & Nomenclature
Preparation -Zn with alkali or HCl ▪ Structural Representations of Organic Compounds Preparation-Alkene Alkyl-halide ▪ Preparation of Haloalkanes -Alkanes(Free radical halo
-Electrolysis, Steam-coke ▪ Classification of Organic Compounds –Aliphatic, Alicyclic (aromatic) -Carboxylic acid (Kolbe electrolysis) -Alkenes (Halogen & hyd
Property -Physical(Colorless Odorless Combustible Gas) ▪ Functional Group (X OH CHO COOH CO CN ROR COO COOR COX NH2) Properties –Melting, Boling p0int & Solubility -Alcohol
-Reaction (N2 O2 X Metal ion & oxide) ▪ Isomerism-Position Metamer Functional group Laevo, Dextro, Cis, Trans -Halogenation, Combustion, Pyrolysis -Halogen exchange (Swa
(Hydrogenation, Hydroformylation) ▪ Homo/hetero-lytic cleavage & Electro/Nucleo-phile -Oxidation, Isomerization, Aromatization ▪ Preparation of Haloarenes -Amines -Sandmeyer's rea
▪ Hydrides(Ionic & Covalent& Metallic) ▪ Effect (Inductive, +/- Resonance, Electrometric, Hyperconjugation) -Conformation -Electrophilic substitution
▪ Water (Structure & Ice) ▪ Reactions (Substitution Addition Elimination Rearrangement) ▪ Alkenes-Nomenclature & Isomerism ▪ Reactions Haloalkane -Nucleophilic (SN1 & SN2), Elim
Property- Amphoteric, Redox, hydrolysis, Hydrate ▪ Purification -Sublimation, Preparation-Alkyne Alkyl-halide(beta-elimination) ▪ Reactions Haloarene -Nucleophilic, Electrophilic & Fr
Soft & Hard Water (Temporary- Boiling & Clark method Crystallization - -Alcohol(dehydration) ▪ Chirality (enantiomer) -Inversion & retention
(Permanent-Sodium Carbonate, Calgon's) Chromatography(adsorption, column, thin layer, Partition) Properties –Melting, Boling p0int & Solubility ▪ optical activity (laveo & dextrorotatory) & Racemizat
(Ion exchange, Synthetic resin) -Distillation(steam, fractional) -Addition(Dihydrogen Halogen H-halide) ▪ Physical Properties -Solubility Melting and Boiling Poi
▪ Hydrogen Peroxide H2O2 (Structure & Uses) ▪ Qualitative Analysis (Test for- H C S P halogen & Lasssaigne Test) - Water addition, Oxidation, Ozonolysis ▪ Polyhalogen Compounds -Dichloromethane, Trichlor
Preparation -Acidifying barium peroxide Peroxodisulphate ▪ Quantitative Analysis (H C N[dumas kejdohl] S P O) -Polymerization -Tetrachloromethane, Freon
-2-alkylanthraquinol Oxidation ▪ Alkynes- Nomenclature & isomerism
Property -Colorless pale blue miscible liquid Preparation -Calcium carbide, Vicinal-dihalide Amines
Alcohols, Phenols and Ethers ▪ Structure Classification & Nomenclature
-Oxidizing action –acidic /basic medium Properties –Melting, Boling p0int & Solubility
▪ Classification & Nomenclature, Methanol & Ethanol ▪ Amines Preparation -Ammonolysis Reduction o
-Reducing action –acidic /basic medium -Addition(Dihydrogen, Halogen, H-halide)
▪ Alcohols Preparation -Alkenes (acid catalyzed &Hydroboration- oxidation) -Hoffmann Bromide , Gabr
▪ Heavy Water(D2O) & Dihydrogen as a Fuel -Water addition, Polymerization
-Aldehyde Ketone (Grignard Reagent& Reduction) ▪ Physical Properties -Basicity (arylamines & alkyla
-Acidic property
-Carboxylic acid & Ester (Reduction) ▪ -Solubility & boiling Point
▪ Aromatic Hydrocarbon -Nomenclature & isomerism
▪ Alcohol Reaction -Acidity, Esterification, Alcohol (&Dehydration) ▪ Chemical Reactions -Alkylation ( R-X pri sec tert
▪ Benzene (Structure, Stability, Resonance)
▪ -Oxidation (Aldehyde & Ketone) -Acylation (Anhydride, ester
Preparation -Ethyne polymerization, Phenol reduction
▪ Phenols Preparation -chlorobenzene, sulphonic acid -Carbylamine, Heinsberg Re
-Aromatic acid decarboxylation
▪ -Diazonium salt, Cumene -Electrophilic Substitution (
Properties -Halogenation, Sulphonation, Combustion
▪ Phenol Reaction -Electrophilic substitution(Br NO2 SO3H) ▪ Diazonium Salt Reaction -Coupling, Sandmeyer,
-Freidel-crafts (acylation, alkylation)
▪ -Kolbe(COOH) & Rieman Tiemann(CHO) Reaction -Replacement by I F H
-ortho para & meta directing group influence
-with Zn dust, Oxidation(benzoquinone)
▪ Carcinogenicity and Toxicity
▪ Ethers Preparation – Alcohol (dehydration & Williamson synthesis)
▪ Ether Reaction -Hydrogen halide & Electrophilic Substitution(Br, NO2 SO3H)
-Freidal Crafts(alkylation acylation)
▪ Physical Properties- Solubility and Boiling Point
Biomolecules
▪ Carbohydrates –Monosaccharides (Glucose Galactose Fructose Ribose)
-Oligosaccharide (Lactose Sucrose Maltose)
-Polysaccharide - (Strach [amylose+ amylopectin] Glycogen)
▪ Amino acids (Essential Non-essential)
Protein –Peptide linkage
-Primary Secondary(Helix & pleated) Tertiary(globular & Fibrous) Quaternary
▪ Enzymes
▪ Nucleic Acids – RNA & DNA (Adenine Guanosine Cytosine Thymine/Uracil)
▪ Hormones & Vitamins (water soluble, fat soluble)
DNA Mutation
DNA Recombinant &
CRISPER
Agarose gel electrophoresis DNA PCR DNA isolation DNA Replication RNA Polypetide chain
protein
1s 2s 2p 3s 3p 4s 3d 4p 5s 4d
1s 2s 2p 3s 3p 4s 3d 4p 5s 4d
7p