The overall goal of biochemistry is to describe life’s processes using the language of molecules, that is, applying the principles ,fundamentals, and methods of chemistry to determine molecular structure from which it is often possible to explain biological function.
Living cell contains thousands of organic and inorganic chemicals, many of them large molecules called macromolecules.
All biological processes, result from how molecules act and, sometimes, misbehave.(why biology and chemistry are prerequisite).
Living cell contains thousands of organic and inorganic chemicals, many of them large molecules called macromolecules.
All biological processes, result from how molecules act and, sometimes, misbehave.(why biology and chemistry are prerequisite).
- معلم: إعتزاز محمد حسان نافع .
-Stereochemistry and stereoisomerism Isomer number and tetrahedral carbon.
-Optical activity,plane-polarized light, the polarimeter and specific rotation.
-Enantiomerism.Chirality.Enantiomers.The racemic modification
-Specification of configuration: R and S. Sequence rules.
-Diastereomers. Meso structure
-Specification of configuration: more than one chiral center. Conformational isomers
-Stereoisomerism, Reactions involving stereoisomers, Generation of a chiral center. Synthesis and optical activity, Reactions of chiral molecules. Bond breaking, Reactions of chiral molecules. Relating configurations, Optical purity, Reactions of chiral molecules. Generation of a second chiral center. Formation of enantiomers and diastereomers. Reactions of chiral molecules with optically active reagents. Resolution. Reactions of chiral molecules. Mechanism of free-radical chlorination. Stereoselective and stereospecific reactions. Syn- and anti-Addition. Mechanism of halogen addition
Stereochemistry of some compounds (Nitrogen, Sulphur phosphorus and Arsenic compounds).
-Optical activity,plane-polarized light, the polarimeter and specific rotation.
-Enantiomerism.Chirality.Enantiomers.The racemic modification
-Specification of configuration: R and S. Sequence rules.
-Diastereomers. Meso structure
-Specification of configuration: more than one chiral center. Conformational isomers
-Stereoisomerism, Reactions involving stereoisomers, Generation of a chiral center. Synthesis and optical activity, Reactions of chiral molecules. Bond breaking, Reactions of chiral molecules. Relating configurations, Optical purity, Reactions of chiral molecules. Generation of a second chiral center. Formation of enantiomers and diastereomers. Reactions of chiral molecules with optically active reagents. Resolution. Reactions of chiral molecules. Mechanism of free-radical chlorination. Stereoselective and stereospecific reactions. Syn- and anti-Addition. Mechanism of halogen addition
Stereochemistry of some compounds (Nitrogen, Sulphur phosphorus and Arsenic compounds).
