TAILIEUCHUNG - Ebook Organic chemistry (2nd edition): Part 1

(BQ) Part 1 book "Organic chemistry" has contents: Structure and bonding; stereochemistry at tetrahedral centers; an overview of organic reactions, alkenes and alkynes; alcohols, phenols, and thiols; ethers and sulfides; structure determination - mass spectrometry, infrared spectroscopy, and ultraviolet spectroscopy,.and other contents. | Structures of Common Coenzymes The reactive parts of the molecules are darkened, while nonreactive parts are ghosted. Adenosine triphosphate—ATP (phosphorylation) NH2 N O –O P O– O P N O O P O N OCH2 N O O– O– OH OH Coenzyme A (acyl transfer) NH2 N O O CH3 N O O N HSCH2CH2NHCCH2CH2NHCCHCCH2OPOPOCH2 HO CH3 N O O– O– 2–O PO 3 OH Nicotinamide adenine dinucleotide—NAD+ (oxidation/reduction) (NADP+) NH2 CONH2 N N O O + N CH2OPOPOCH2 N OH HO O N O O– O– OH OH (OPO32–) Flavin adenine dinucleotide—FAD (oxidation/reduction) NH2 N HO OH HO CHCHCHCH2OPOPOCH2 O– O– CH2 H3C N H3C N N N O O OH N O N O O H OH N Tetrahydrofolate (transfer of C1 units) H H2N H N N H N N N CO2– H O H O NHCHCH2CH2C O– 1–5 O S-Adenosylmethionine (methyl transfer) NH2 N N CH3 O –OCCHCH CH 2 2 +NH S + CH2 N N O 3 OH OH Lipoic acid (acyl transfer) S Pyridoxal phosphate (amino acid metabolism) CH2OPO32– S CHO CH2CH2CH2CH2CO2– + H N OH CH3 Biotin (carboxylation) Thiamin diphosphate (decarboxylation) H S O NH2 + N H N O O –OPOPOCH CH 2 2 O– O– N N H CH3 N H H H CH3 S CH2CH2CH2CH2CO2– even in our courses, Dear Colleague: t of the students pure ow that mos es rather than in nic chemistry kn in the life scienc who teach orga ily doctors All of us terested primar ochemists, and e y majors, are in re biologists, bi the chemistr estioning why w ng so many futu se we are teachi more of us are qu the details of s, more and chemistry. Becau time discussing ions of ourselve y? Why spend so much an younger vers rather th ection to biolog do. Why do we t have little conn ach the way we organisms? chemists bu continue to te emistry of living terest to research ng the organic ch ons that are of in reacti me discussi it is d spend more ti itional way, but don’t we instea istry in the trad want to organic chem e instructors who id for teaching l much to be sa ternative for thos cal There is stil s been no real al try .

• Hoá học
• Organic chemistry
• Tetrahedral centers
• An overview of organic reactions
• Structure determination
• Infrared spectroscopy
• Ultraviolet spectroscopy
• In this workbook
• experiments are elaborated using small scale glassware and equipments from a Small Lab Kit
• developed at the Department of Chemistry
• Faculty of Science
• Chulalongkorn University in Thailand
• This Small Lab Kit was created as a result of the research project entitled “Chemistry Laboratory Based on Chemical Safety and Pollution Minimization” sponsored by Thai Research Fund (RDG 3 07 2543)
• One of the outcomes of this project is the organic laboratory book entitled “Organic Chemistry Laboratory Based on Chemical Safety and Pollution Minimization” written in Thai by professors from 7 universities in this project
• They compiled
• adjusted and tested the experiments taken from several traditional organic chemistry laboratory books using the prototype of Small Lab Kit
• Currently
• some selected experiments from this Thai organic chemistry laboratory text have further been modified
• rewritten and edited in English as appeared in this workbook
• Some experiments ar
• Ebook Organic chemistry
• Nucleophilic substitution
• Determining organic structures
• nucleophilic addition
• Organic structures
• Electrophilic aromatic substitution
• Principles of organic chemistry
• Methods of organic chemistry
• The methane series
• The acetylene series
• Polybasic acids
• High school
• University entrance exam
• Teaching organic chemistry
• Organic chemistry exam question
• Interdisciplinary science
• Advanced practical organic chemistry
• Functional groups
• Organic synthesis reagents
• The structure
• Reactions of organic names
• Fundamentals of organic chemistry
• Carbonyl alpha substitution reactions
• Condensation reactions
• The organic chemistry
• Organic chemistry principles in context
• Starch to the principles
• The structures of organic molecules
• Mass spectrometers
• Infrared spectrometers
• Nuclear magnetic resonance spectrometers
• Modern physical organic chemistry
• Strain and stability
• Covalent binding forces
• Electronic organic materials
• Thermal pericyclic reactions
• The study of organic chemistry
• Stereochemistry and resonance
• Identification of organic compounds
• Elimination reactions
• Electrophilic addition reactions
• Electron delocalization
• Organic compounds
• Cyclic hydrocarbons
• Aromatic alcohols
• Aromatic compounds containing
• Inorganic chemistry
• A guidebook to mechanism in organic chemistry
• Aromatic systems
• Linear free energy relationships
• Symmetry controlled reactions
• Fatty acid catabolism
• The chemistry of the carbonyl group
• The industrial road toward increasing efficiency
• Lecture Organic chemistry
• Hóa học hữu cơ
• Bài giảng Hóa học hữu cơ
• Chemistry of benzene
• Derivatives of benzene
• Summary of Organic Chemistry Dotoral Thesis
• Organic Chemistry Dotoral Thesis
• Natural Products Chemistry
• Biological evaluation
• Chemistry of natural compounds
• Ideas in chemistry
• Molecular sciences
• Synthetic chemistry
• Innovative processes in organic chemistry
• Predictive tools
• Organic chemical reactions
• Electronic Structure
• Electronic configurations of atoms
• Electronic configurations
• Wave properties of electrons
• Wave interactions
• Stereochemistry of alkanes
• Alkane conformations
• Chemical reactions
• Chlorination of Methane
• Chiral carbons
• Nonmobile conformers
• Alkyl Halides