Importance of Core Revision Points: Core Revision Points are important because if you remember them strongly, many more points related to them will come out of your memory and help you to answer question and problems. Read them many times and make sure you remember them very strongly.
Core Revision Points in Sections in the Chapter
12.1 Types of isomerism
Isomers are two types: constitutional (structural) and stereoisomers.
12.2 Geometrical isomerism
13.3 Confirmational isomerism
12.4 Optical activity
12.5 Chirality of objects and molecules
A chiral molecule is a molecule that is non superimposable on its mirror image.
12.6 Enantiomers
12.7 Configurations and Fisher Projections
12.8 Chiral or asymmetric carbon
The carbon atom which is bonded to four different groups or atoms is called chiral or asymmetric carbon.
12.9 Symmetry elements and chirality
12.10 Dissymetry – Condition for enantiomerism
12.11 Nomenclatures for stereo- isomers
12.12 Compounds containing two chiral centres
12.13 Meso compounds
Meso compound is a compound whose molecules are superimposable on their mirror images inspite of the presence of an assymmetric carbon atom. This is due to internal compensation.
12.14 Racemic mixtures and racemisation
12.15 Resolution
12.16 Importance of Stereo Chemistry
Sections in the Chapter
12.1 Types of isomerism
12.2 Geometrical isomerism
13.3 Confirmational isomerism
12.4 Optical activity
12.5 Chirality of objects and molecules
12.6 Enantiomers
12.7 Configurations and Fisher Projections
12.8 Chiral or asymmetric carbon
12.9 Symmetry elements and chirality
12.10 Dissymetry – Condition for enantiomerism
12.11 Nomenclatures for stereo- isomers
12.12 Compounds containing two chiral centres
12.13 Meso compounds
12.14 Racemic mixtures and racemisation
12.15 Resolution
12.16 Importance of Stereo Chemistry
Notes
https://www.utdallas.edu/~scortes/ochem/OChem1_Lecture/Class_Materials/09_stereo_notes.pdf
Updated on 2 January 2020
31 January 2016
Core Revision Points in Sections in the Chapter
12.1 Types of isomerism
Isomers are two types: constitutional (structural) and stereoisomers.
12.2 Geometrical isomerism
13.3 Confirmational isomerism
12.4 Optical activity
12.5 Chirality of objects and molecules
A chiral molecule is a molecule that is non superimposable on its mirror image.
12.6 Enantiomers
12.7 Configurations and Fisher Projections
12.8 Chiral or asymmetric carbon
The carbon atom which is bonded to four different groups or atoms is called chiral or asymmetric carbon.
12.9 Symmetry elements and chirality
12.10 Dissymetry – Condition for enantiomerism
12.11 Nomenclatures for stereo- isomers
12.12 Compounds containing two chiral centres
12.13 Meso compounds
Meso compound is a compound whose molecules are superimposable on their mirror images inspite of the presence of an assymmetric carbon atom. This is due to internal compensation.
12.14 Racemic mixtures and racemisation
12.15 Resolution
12.16 Importance of Stereo Chemistry
Sections in the Chapter
12.1 Types of isomerism
12.2 Geometrical isomerism
13.3 Confirmational isomerism
12.4 Optical activity
12.5 Chirality of objects and molecules
12.6 Enantiomers
12.7 Configurations and Fisher Projections
12.8 Chiral or asymmetric carbon
12.9 Symmetry elements and chirality
12.10 Dissymetry – Condition for enantiomerism
12.11 Nomenclatures for stereo- isomers
12.12 Compounds containing two chiral centres
12.13 Meso compounds
12.14 Racemic mixtures and racemisation
12.15 Resolution
12.16 Importance of Stereo Chemistry
Notes
https://www.utdallas.edu/~scortes/ochem/OChem1_Lecture/Class_Materials/09_stereo_notes.pdf
Updated on 2 January 2020
31 January 2016
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