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25 Cards in this Set

  • Front
  • Back
isomers
different compounds with same molecular formula
(constitutional and stereoisomers)
constitutional isomers (3)
-different IUPAC names
-same or different F.G.'s
-different chemical and physical properites
Stereoisomers
-differ only in the way the atoms are oriented in space (configuration)
Configuration
a particular 3-D arrangement
Chiral Molecules
a molecule that is non superimposable on its mirror image
Achiral molecule
a molecule that IS superimposable on its mirror image
Enantiomers
mirror images that are not superimposable (chiral molecules)
stereogenic center
a tetrahedral carbon atom with four different groups attached to it.
R isomer
used to name enantiomers that have priorities arranged in a clockwise manner
S isomer
used to name enantiomers that have priorities arranged in a counterclockwise manner
diasteromers
stereoisomers that are NOT mirror images of each other
Meso Compounds
an achiral compound that contains tetrahedral centers
observed rotation
the angle that chiral compounds rotate light
optically active
a compound that rotates plane polarized light (chiral)
dextrorotarary (+)
a compound that rotates plane polarized light clockwise
levorotatary (-)
a compound that rotates plane polarized light anticlockwise
racemic mixture
equal amounts of 2 enantiomers
specific rotation
standardized physical constant for the amount that a chiral compound rotates plane polarized light
concerted reaction
starting material converted directly to product in one step
A - B
stepwise reaction
A - reactive intermediate - B
homolysis
breaking a bond by equally dividing the electrons between the 2 atoms in the bond
heterolysis
breaking a bond by unequally dividing the electrons in a bond between the two atoms
bond dissociation energy
The energy needed to homolytically cleave a covalent bond
What 2 halides are sp2 hyrbridized?
vinyl halides
aryl halides
What 2 halides are sp3 hybridized?
(thus reactive)
allylic halide
benzylic halide