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Organic

Structure, classification and naming of organic compounds. IUPAC nomenclature

Lecturer: Doctor of Chemistry, prof. A.A. Popov атом [ˈætəm] ионный ionic [aɪˈɔnɪk] молекула [ˈmɔlɪkju:l] изотоп isotope [ˈaɪsəutəup] электрон electron [ɪˈlektrɔn] жидкость liquid [ˈlɪkwɪd] ядро nucleus [ˈnju:klɪəs] моль mole [məul] ядра nuclei [ˈnju:klɪaɪ] молекулярный molecular [məuˈlekjulə] протон proton [ˈprəutɔn] нейтральный neutral [ˈnju:trəl] нейтрон neutron [ˈnju:trɔn] окисление oxidation [ˌɔksɪˈdeɪʃən] валентность valency [ˈveɪlənsɪ] периодический periodic [ˌpɪərɪˈɔdɪk] кислота acid [ˈæsɪd] многоатомный polyatomic [ˌpɔlɪəˈtɔmɪk] основание base [beɪs] реакция reaction [ri:ˈækʃən] щелочь alkali [ˈælkəlaɪ] реакционная reactivity [ˌri:ækˈtɪvɪtɪ] соль salt [sɔ:lt] способность поваренная соль common salt [ˈkɔmən sɔ:lt] восстанавливать reduce [rɪˈdju:s] анион anion [ænaiən] восстановитель reducing agent [rɪˈdju:siŋ катион cation [ˈkætaɪən] ˈeɪdʒənt] двухатомный diatomic [ˌdaɪəˈtɔmɪk] твердое solid [ˈsɔlɪd] формула formula [ˈfɔ:mjulə] вещество, формулы formulae [ˈfɔ:mjuli:] твердый газообразный gaseous [ˈɡæsjəs] вещество substance [ˈsʌbstəns] кремний silicon [ˈsɪlɪkən] водород hydrogen [ˈhaɪdrɪdʒən] фосфор phosphorus [ˈfɔsfərəs] гелий helium [ˈhi:ljəm] сера sulphur [ˈsʌlfə] литий lithium [ˈlɪθɪəm] хлор chlorine [ˈklɔ:ri:n] бор boron [ˈbɔ:rɔn] аргон argon [ˈɑ:ɡɔn] углерод carbon [ˈkɑ:bən] калий potassium [pəˈtæsjəm] азот [ˈnaɪtrədʒən] кальций calcium [ˈkælsɪəm] кислород [ˈɔksɪdʒən] галлий gallium [ˈɡælɪəm] фтор fluorine [ˈfluəri:n] мышьяк arsenic [ˈɑ:snɪk] бром bromine [ˈbrəumi:n] неон neon [ˈni:ən] йод iodine [ˈaɪəudi:n] натрий sodium [ˈsəudjəm] медь copper [ˈkɒpə] магний magnesium [mæɡˈni:zjəm] медный cupric [ˈkjuːprɪk] алюминий aluminium [ˌæljuˈmɪnjəm] Theory of the chemical of organic compounds (Butlerov A.M.)

 1. All in the molecule of are bound with each other in determined sequences in accordance with their .  2. Properties of substance depend on the . Chemical structure - is a certain order in the alternating of atoms in the molecule, in the interaction and mutual influence of atoms a to each other - as nearby, so and through other atoms.  3. Study of substances properties allows defining their chemical structure, but the chemical structure of substances defines their physical and chemical properties.  4. Carbon atoms are capable to be connected between itself, forming carbon with different type chains.  5. Each organic compound has one determined structured formula, which builds, basing on the position about four-valence carbon and on the ability of its atoms to form chains and cycles. Structural formulas

 The way the atoms are bonded together in a compound is shown by its .

 Single straight line connecting the atomic symbols is used to represent a single (two-electron) bond, two such lines to represent a double (four- electron) bond, and three lines a triple (six- electron) bond Examples of structural formulas for some organic compounds

Structural formula of vanillin (4- Hydroxy-3-methoxybenzaldehyde) Structural formulas. Homologous series of alkanes Structural formulas. Homologues series of alkenes

['ɛθi:n]

['bju:ti:n] ['pɛnti:n]

[‘heksi:n] IUPAC Nomenclature

4- isopropyl-3-ethyl octane «Identification of the parent functional group, if any, with the highest order of precedence»

Naming of organic compound in accordance to IUPAC principles

2,7,8 trimethyldecane Isomerism of organic compounds Isomerism of organic compounds

have different structural formulae because their atoms are linked together in different ways •arrangement of Carbon skeleton

•position of Functional group

Isomerism of organic compounds

different Functional groups Stereoisomerism

Stereoisomers have the same structure and bond order but their atoms and groups of atoms are arranged differently in space. Optical isomerism

Involves an atom, usually carbon, bonded to four different atoms or groups of atoms. They exist in pairs, in which one isomer is the mirror image of the other