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27 Cards in this Set

  • Front
  • Back
chirial
you're mirror image can't be superimposed on you.
enantiomer
a non-superimposable mirror image
meso compound
achiral compound that contains tetrahedral stereogenic centers
diasteriomers
stereoisomers that are not enantiomers
alkyl halide
organic molecule with a halogen bonded to an sp3 carbon
Vinyl halide
organic molecule with a halogen bonded to a carbon=carbon double bond
aryl halide
organic molecule with a halogen bonded to a benzene ring
Allylic halide
organic molecule with a halogen bonded to a carbon that is bonded to a carbon=carbon double bond
benzylic halide
organic molecule with a halogen bonded to a carbon atom that's bonded to a benzene ring.
What are the periodic trends for L.G. ability?
increases across a row, increases down a column.
What do protic solvents do to nucleophilicity?
they cause nucleophilicity to increase DOWN the periodic table.
What do aprotic solvents do to nucleophilicity?
they cause nucleophilicity to increas UP the periodic table.
What mechanism uses backside attack?
Sn2
What alkenes are more stable?
Trans and more substituted
When is E2 not possible?
When there are no H's on the Beta C.
Does increased base strength increase or decrease E2 rate?
increase
Do polar aprotic solvents increase or decrease E2 rate?
increase
Does leaving group ability increase or decrease E2 rate?
increase
Does increased number of R groups on alpha carbon increase or decrease E2 rate?
increase
Does increased number of R groups on alpha carbon increase or decrease Sn2 rate?
decrease
Zaitsev Rule
The major product of a beta elimination is the one with the more substituted double bond.
Does increasing the number of R groups on the beta carbon increase or decrease E1 rate?
increase
Does base strength increase or decrease E1 rate?
decrease
Does increased leaving group ability increase or decrease E1 rate?
increased
Do aprotic or protic solvents favor E1?
protic (to solvate carbocation)
racemic mixture
1:1 mixture of enantiomers
doesn't rotate light
Physical properties of diasteriomers are...
all different