Stereochemistry Flashcards
chirality
the ability to exist in two non-superimposable mirror-image forms
entaniomers
a pair of non-superimposable mirror-image molc
sterioisomers
isomers that have the same connectivity of atoms but different spacial arrangements
asymmetric carbons
a carbon that has 4 different groups attached to it
aka chiral carbons
chiral center
an atom holding a set of groups in a spacial arrangement that is not superimposable on its own mirror image
stereocenter
any atom at which the interchange of two groups gives a stereoisomer
the 2^n rule
a molecule with n chiral centers can have a maximum of 2^n stereoisomers
absolute configuration
description of the spacial arrangement of the groups attached to a chiral center
R/S nomenclature convention
used to assign absolute configuration
uses the Cahn-Ingold-Prelog Priority system to prioritize groups attached to the chiral carbon
Optical activity
rotation of the plane of plane-polarized light
optically active
a molecule rotates the plane-polarized light
dextrorotatory enantiomer
an enantiomer that rotates plane-polarized light clockwise (+)
levorotatory enantiomer
an enantiomer that rotates the plan-polarized light counterclockwise (-)
Racemic mixture
equal amounts of (+) and (-) enantiomers
specific rotation
rotation induced by 1 g/ my of solution