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24 Cards in this Set

  • Front
  • Back
draw : hemiacetal
What is the reaction to make a hemiacetal?
RCHOHOR'
reaction : aldehyde + alcohol
draw : hemiketal
What is the reaction that makes a hemiketal?
RCOHROR'
reaction : ketone + alcohol
draw : a mesyl group
CH3O=S=O
draw : a tosyl group
CH3-Ph-O=S=o
carbonyl group
--C=O
acetyl group
--COCH3
acyl group
--COR
anhydride
R-COOOC-R
aryl
phenyl group, benzene ring as a functional group
benzyl
aryl group + CH2 -- R
enamine
amine attached to an alkene
imine
nitrogen double bonded to a carbon
oxime
nitrogen double bonded to a carbon and also attached to a hydroxyl group. R2C=N-OH
nitro
N double bonded to an O and single bonded to another O (NO2)
nitroso
N double bonded to an O (NO)
how are atoms around the chiral center given priorities?
1) atomic weight
2) subs on double and triple bounds are counted two and three times respectively
enantiomers
same molecular formula, same bond-to-bond connectivity, mirror images, NOT the same molecule
Enantiomers have (the same/different) physical and chemical properties? What are the exceptions?
the same
exceptions : in reactions with plane polarized light, with other chiral compounds
diastereomers
same molecular formula, same bond-to-bond connectivity, NOT mirror images, and NOT the same compound
resolution
the separation of enantiomers
geometric isomer
a typ of diastereomer
cis/trans
DIFFERENT physical properties
meso compounds
have a plane of symmetry through their centers which divides them into two halves that are mirror images to each other
achiral, so optically inactive
epimer
diastereomers that differ at only one chiral carbon
anomer
- a type of epimer
- stereoisomer of a cyclic saccharide