• Shuffle
    Toggle On
    Toggle Off
  • Alphabetize
    Toggle On
    Toggle Off
  • Front First
    Toggle On
    Toggle Off
  • Both Sides
    Toggle On
    Toggle Off
  • Read
    Toggle On
    Toggle Off
Reading...
Front

Card Range To Study

through

image

Play button

image

Play button

image

Progress

1/10

Click to flip

Use LEFT and RIGHT arrow keys to navigate between flashcards;

Use UP and DOWN arrow keys to flip the card;

H to show hint;

A reads text to speech;

10 Cards in this Set

  • Front
  • Back
Chiral carbons =
carbons with four different groups attached are chiral.
The mirror image will be a different compound (enantiomer).
has chiral carbons, no plane of symmetry
Achiral compounds
molecules can be superimposed
- a molecule that has a plane of symmetry.
Isomers =
compounds with the same formula
Constitutional isomers =
same formula, but different in the way the atoms are attached
CH3OCH3 CH3CH2OH
Stereoisomers =
same formula, same point of attachment, difference in spatial arrangement
Enantiomers =
nonsuperimposable mirror images, different molecules with different properties.
- have the following properties:
-Same boiling point
-Same melting point

-Different rotation for the plane of polarized light
Conformation isomers =
same formula, same point of attachment, difference in spatial arrangement, and interconverts at room temperature
-same formula, same point of attachment, difference in spatial arrangement, and cannot interconvert at room temperature
Cahn-Ingold-Prelog Rule 1
Compare the first atoms. The atom with the highest atomic weight has the highest priority.
Cahn-Ingold-Prelog Rule 2
If the first atoms are the same, compare the next atoms.
Cahn-Ingold-Prelog Rule 3
For double bonds, add one set of imaginary atoms. For triple bonds, add two sets of imaginary atoms.