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what are stereoisomers
same structural formula, different spatial arrangement
why do E/Z isomers have restricted rotation
because of a double bond
what is a chiral carbon
carbon that has 4 different groups attached

what are optical isomers
non-superimposable mirror images
how does plane-polarised light rotate
only in one direction
vertically, horizontally or anything in between
difference between normal light and plane polarised light
normal light roattes in all directions
plane-polarised light roattes only in one
what can optical isomers do to be able to call them optically active
rotate plane polarised light
in what direction do 2 enantiomers rotate plane-polarised light
in opposite directions
define racemic mixture
contains equal quantities (50:50) of each enantiomer of an optically active compound
why do racemates not show any optical activity
2 enantiomers cancel each out other light-rotating effect
why is racemic mixture 50:50 of each enantiomer
when 2 molecules react there is an equal chance of a bond both above and beyond the planar