1/23
Flashcards based on key concepts related to carbohydrates and monosaccharides, designed to assist in exam preparation.
Name | Mastery | Learn | Test | Matching | Spaced |
---|
No study sessions yet.
Carbohydrates
Most abundant biomolecules on earth, produced from CO2 and H2O via photosynthesis, frequently referred to as 'sugars'.
Monosaccharides
The simplest carbohydrates, consisting of a single polyhydroxy aldehyde or ketone unit.
Epimers
Two sugars that differ in configuration at one specific carbon atom.
Anomers
Stereoisomers that differ in configuration at the anomeric carbon.
Hemiacetal
A product formed when an aldehyde reacts with an alcohol.
Mutarotation
The change in optical rotation that occurs when an anomeric carbon converts between its alpha and beta forms.
Chirality
The property of a molecule having non-superimposable mirror images.
D- and L-Configuration
Configurations based on the orientation of the hydroxyl group on the penultimate carbon
Reducing sugars
Any sugar capable of acting as a reducing agent due to having a free aldehyde or ketone group.
Fischer Projection
A two-dimensional representation of a monosaccharide's stereochemistry, chiral carbs
Haworth Projection
A three-dimensional representation of a cyclic monosaccharide structure.
Diastereomers
Stereoisomers that are not mirror images of each other, differ at one or more chiral centers and have different physical properties
Disaccharides
2 units of monosaccharides
Oligosaccharides
Short chains (3-20) of monosaccharide units
Polysaccharides
Long chains of monosaccharide units
Aldose
Carb with aldehyde functionality
Ketose
Carb with ketone functionality
D-sugar configuration
OH group of the right of the penultimate carbon
L-sugar configuration
oh group of the left of the penultimate carbon
Stereoisomerism
Same atom connectivity, different spatial arrangements
D-aldoses
Retain the D-glyceraldehyde configuration at the penultimate carbon
Anomeric carbon
Carbonyl carbon in the linear form
Alpha-anomer
An anomer where the hydroxyl group on the anomeric carbon is positioned below the plane of the sugar ring.
Beta-anomer
The anomer where the hydroxyl group at the anomeric carbon is on the same side as the C6 carbon in the cyclic form.