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Fischer's projection
Common projection to represent carbohydrate
Fischer's projection, aldehyde
places the - group (most oxidized) at the top.
Fischer's projection
shows the - H and -OH groups on the horizontal intersecting line.
Achiral, Fischer's projection
places the - -CH2OH group at the bottom
Isomer
Compounds that are composed of the same atoms but still differ from each other.
Structural or stereo
2 kinds of isomer
Geometric and optical isomer
In stereoisomer we bave
Structural isomers
Compounds with the same molecular formula but different connectivity
Stereoisomer
Molecules with the same formula and same connectivity but only differ on their spatial arrangement
Geometric, optical
Could either be - isomer or - isomer.
Geometric isomers
Molecules that differ in spatial arrangement around a rigid bond (usually a double bond) or a ring
Z = zuzamen = same side
E = magkalayo = snake = opposite
E/Z
Platin, cisplatin (same side cl)
One is used to treat cancer, one isn't
Optical isomer
Non-superimposable mirror images due to presence of chiral center
Rotate plane-polarized light in (+) or (-) direction
Dextrorotatory
If a chiral compound rotates the plane-polarized light clockwise (+), it is -
Levorotatory
If a chiral compound rotates the plane-polarized light counterclockwise (-), it is -
R, s
This is in no way connected to the - and - configuration. It may only be determined using experiment.
Dextrorotatory
Levorotatory
D IS FOR
L IS FOR
D config L config
Second to the last
OH nasa right =
OH nasa left =