Common Molecules Flashcards
What is meant by carboxylation?
Addition of –COO group
What is meant by decarboxylation?
Removal of –COO group

Acetaldehyde
formed from breakdown of ETOH

Acetoacetate
formed during ketogenesis

Acetone
formed during ketogenesis

Acetyl CoA

Acetylcholine

Adenine

Adenosine

ATP
Adenosine Triphosphate

Amylose
alpha-1,4 glycosidic

Beta-Hydroxybutyrate
formed during ketogenesis

Beta Lactam
ABx

cAMP

Cytidine

Cytosine
ID the molecule shown
Which is the anomeric carbon?

D-Glucose
we know this because the OH is on the right in the fisher projection
Carbonyl carbon
this is the carbon that is attacked intramolecularly by carbon 5
ID the molecule shown
Which carbon is the anomeric carbon?

D-glucose
we know it’s D-glucose because the highest numbered carbon (upper left corner) is R.
Carbon 1 is the anomeric carbon
the carbon that has 2 oxygens attached to it (right-most carbon) You can prove this by viewing D-glucose in fisher projection form and performing an intramolecular nucleophillic attack.

Epinephrine

Fructose

Furan

Furanose ring
comparison group for sugar naming (Aldofuranose/ Ketofuranose)
“<strong>F</strong>uran, <strong>F</strong>ive” because it’s a 5-membered ring
ID the molecule shown
Which carbon tells alpha vs. beta?
Which carbon tells D/L?

Alpha-D-Galactose
the 4th carbon is emphasized because this is the differential between glucose and galactose. Glucose has an equatorial OH, while Galactose has an axial OH.
Alpha/Beta is determined by carbon 1 (anomeric carbon)
it’s always good to “B Up”
D/L is determined by carbon 5, the penultimate carbon
Figure out chirality of the stereocenter. (R in this case)

Beta-D-Glucose
we know it’s D-glucose because the highest numbered carbon is R.
we know it’s Beta because the OH on carbon 1 (anomeric carbon) is up, and “It’s always good to B UP” because Beta sugars are more stable than Alpha sugars.





























