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ORGANIC CHEMISTRY II

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Learning Outcomes

  • Be able to name the drugs.
  • Explains the trade name
  • Reveals the official name
  • Explains non-commercial name
  • Explains the Pharmacopoeia name
  • Explains the generic name
  • Reveals international non-commercial name
  • Explains the chemical name
  • Be able to name organic compounds.
  • Explains proper names
  • Explains derived names
  • Explains IUPAC nomenclature
  • Explain IUPAC Naming Rules.
  • Determines the basic chain or structure
  • Identifies groups attached to the base chain or structure
  • Determines the priority atom in numbering
  • Determines the numbering of the main chain/structure and the subordinate groups
  • Explain Functional Groups.
  • Classifies groups
  • Explains the order of precedence between groups
  • Explain cyclic compounds.
  • Classify cyclic compounds
  • Name the cyclic compounds
  • Determines the priority atom in numbering
  • Determines the numbering of the main structure and subordinate groups.
  • Explain aromatic compounds.
  • Name the aromatic rings
  • Determines the priority atom in numbering
  • Determines the numbering of the main structure and subordinate groups.
  • Explain Condensed Compounds.
  • Determines the condensed rings
  • Determines the priority atom in numbering
  • Determines the numbering of the main structure and subordinate groups.
  • Name the condensed system
  • Explain the molecular structure.
  • Explains the molecular structure of the organic compound given its name
  • Explain geometric isomerism.
  • Explains Cis, Trans isomerism
  • Describes E, Z isomers
  • Cahn Ingold Prelog explains the order of precedence
  • Explain Optical Isomerism.
  • Explains chirality
  • Explains the concepts of dextrogyr and levogyr
  • Explains the symbols R, S
  • Explains the symbols D, L
  • Explain the concept of racemics in organic compounds
  • Explain the concept of Enantiomer in organic compounds.
  • Explain UV (Ultraviolet) Spectroscopy.
  • Lambert explains Beer's law
  • Explain the technique of obtaining UV Spectrum.
  • Explains electronic stimulation
  • Define conjugation
  • Define hyperconjugation
  • Explain chromophore groups
  • Explain auxochrome groups
  • Explain bathochromic and hypsochromic shifts
  • Explain hypercormic and hypochromic effects
  • Explain the applications of UV spectroscopy
  • Explain the use of the UV spectrum in structure evaluation
  • Explain IR (Infrared) Spectroscopy.
  • Explains the basic principles of IR Spectroscopy.
  • Explain the technique of receiving IR Spectrum.
  • Explains absorption in the infrared region
  • Explains stretching vibrations
  • Explains bending vibrations
  • Explain the types of infrared bands (combination tone, overtone)
  • List the factors affecting frequency
  • Fermi defines resonance
  • Explain the stretching vibration band regions of alkanes.
  • Explain the stretching vibration band regions of alkenes.
  • Explain the stretching vibration band regions of alkynes
  • Explain the stretching vibration band regions of aromatic compounds
  • Explain the stretching vibration band regions of alcohols and phenols
  • Explain the stretching vibration band regions of the ethers
  • Explain the stretching vibration band regions of mercaptans and thioethers
  • Explain the stretching vibration band regions of amines
  • Explain the stretching vibration band regions of aldehydes
  • Explain the stretching vibration band regions of ketones
  • Explain the stretching vibration band regions of carboxylic acids.
  • Explain the stretching vibration band regions of esters
  • Explain the stretching vibration band regions of amides
  • Explain the applications of IR spectroscopy
  • Explain the use of IR spectroscopy in structure determination.
  • Explain NMR Spectroscopy.
  • Define nuclear magnetic resonance.
  • Describes 1H-NMR and 13C-NMR spectra
  • Explain the basic principles of 1H NMR Spectroscopy.
  • Explain the technique of taking 1H NMR Spectrum.
  • List the properties of the solvents used during the 1H NMR Spectra acquisition process.
  • Explains chemical shift and ppm values ​​of some functional groups
  • Explain diamagnetic anisotropy.
  • Explains the peak shapes and splitting states (spin-spin interactions) of functional groups
  • Explains the relative areas of the peaks (peak intensity)
  • Explain the effect of electronic effects on chemical shift.
  • Explain diamagnetic and paramagnetic shifts
  • Explain the use of 1H NMR spectroscopy in structure determination.
  • Explain MS (Mass) Spectroscopy.
  • Describes the principles of MS (Mass) spectroscopy
  • Defines the molecular ion (parent ion) and its peak
  • Defines the main peak
  • Explains the metastable peak
  • Explain the use of MS (Mass) spectroscopy in molecular weight determination and the nitrogen rule.
  • Defines the principles that apply to the breakdown of molecules.
  • Identify rearrangement reactions in MS (Mass) spectroscopy
  • Describe the different techniques used in MS (Mass) spectroscopy
  • Explain the use of MS (Mass) spectroscopy in structure determination.
  • Explain Other Methods.
  • Explain the use of elemental analysis in structure determination.
  • Explain X-ray diffraction and its use in crystal structure determination.
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