1/24
A set of vocabulary flashcards covering stereochemistry, isomerism, fatty acids, chirality, and carbohydrate structural projections from the lecture notes.
Name | Mastery | Learn | Test | Matching | Spaced | Call with Kai | Chat |
|---|
No analytics yet
Send a link to your students to track their progress
Isomers
molecules have the same molecular formula but their atoms are arranged differently
cis isomer
important groups are located on the same side
trans isomer
important groups are located on opposite sides of a double bond
cis fatty acid
has a bend kink in its chain
trans fatty acid
chain is straight
saturated fatty acid
it has no c=c double bond
unsaturated fatty acid
it has one or more c=c double bond
steroisomers
same molecular formula and connectivity but different 3d arrangement
cis-trans isomers
type of steroisomer caused by restricted rotation
Ring compound
cis/trans can also occur when groups are attached to a ring
restricted rotation
cis trans occurs because c=c double bonds can't freely rotate
dipole moment
measure of separation of oos and nega charge in molecule
chiral carbon
carbon that is attached to 4 different groups
achiral carbon
carbon that isn't attached to 4diff groups
chiral center
changes overall 3d structure, atom where diff arrangements of attached groups can produce diff steroisomers c2-c5
enantiomers
non-superimposable mirror images
diastereomers
stereoisomers that are not mirror images
fishcher projection
ways of representing sugar in straight chain form (2d-3d) using horizontal n vertical lines to show 3D arrangement
horizontal bonds
facing towards the viewer
vertical bonds
facing away the viewer
D-sugar
sugar OH group on the chiral carbon farthest from the carbonyl is on the right
L-sugar
sugar whose OH group on the chiral carbon farthest from the carbonyl is on the left
haworth projection
ways of representing sugar in its cyclic ring form
rlrr
oh arrangement c2-c5 D-glucose
rlrl
oh arrangement c2-c5 L-glucose