Chapter 7 Flashcards
Carbohydrates act as an _____ source, a structural component of ______ and exoskeletons, and act as informational molecules in ______ signaling
Energy
Cell walls
Cell to cell
Carbohydrates can bond with ____ and ____
Proteins and lipids
An aldose contains an ____ while a ketose contains a _____
Aldehyde
Ketone
A molecule with n chiral centers has ____ stereoisomers
2^n
When the hydroxyl group is on the right, it’s a __ sugar, and an __ sugar when the hydroxyl is on the left, and this designation is made from the last chiral carbon in the chain
D –> right
L–> left
What is an epimer?
Two molecules with the same formula, but that differ at an asymmetrical carbon
They are under the branch of isomers and diastereomers
What is an anomer?
Isomers (have the same molecular formula) that differ in their configuration around the anomeric carbon
ex: alpha and beta Glucose
In the beta configuration, the anomeric OH is on the ____ side of the CH2OH
Same
In the alpha configuration, the anomeric OH is on the ____ side of the CH2OH
Opposite
How can you identify the anomeric carbon?
It’s the one to the right of the oxygen in the ring
A pyran represents a sugar with ___ atoms, while a furan represents a sugar with __ atoms
6
5 (Furan –> Five)
What is the difference between a hemiacetal and a hemiketal?
A hemiacetal is formed when an alcohol reacts with an aldehyde, and a hemiketal is formed when an alcohol reacts with a ketone
What is mutarotation and what must the ring do before this can occur?
Mutarotation occurs when the ring shifts back and forth between its alpha and beta forms. This requires the ring to open first
If the OH groups point to the left in the Fischer projection, it will point __ in the Haworth projection, and if the OH points right in the Fischer projection, it will point ___ in the Haworth projection
Up
Down
(This refers to all the OH groups on the Fischer projection)
In a ring, the bulky groups prefer to be ____ to prevent steric hinderance
Equitorial