Chapter 4: Carbohydrate Structure and Function Flashcards
(27 cards)
The simplest monosaccharides contain 3 carbon atoms and are called __________.
Triose
Carbohydrates with 4, 5, and 6 carbon atoms are called ___________, __________, and ____________, respectively.
- Tetrose
- Pentose
- Hexose
The simplest aldose (aldehyde sugar) is _______________ and the simplest ketose (ketone sugar) is ________________.
- Glyceraldehyde
- Dihydroxyacetone
______________, also called ________________, are compounds that have the same chemical formula; these molecules differ from one another only in terms of the spatial arrangement off their component atoms.
- Optical isomers
- Stereoisomers
A special type of isomerism exists between stereoisomers that are nonidentical, nonsuperimposable mirror images of each other. These molecules are called ________________.
Enantiomers
When trying to figure out how many possible stereoisomers can exist for a multi-carbon compound, identify the number of ______________ (n) and plug into the formula 2^n.
Chiral carbons
3 types of stereoisomers:
- The same sugars, in different optical families, are ___________________ (such as D-glucose and L-glucose)
Enantiomers
3 types of stereoisomers:
- Two sugars that are in the same family (both are either ketoses or aldoses, and have the same number of carbons) that are not identical and are not mirror images of each other are _______________.
Diastereomers
3 types of stereoisomers:
- A special subtype of diastereomers are those that differ in configuration at exactly one chiral centre. These are defined as ___________ (such as D-ribose and D-arabinose, which only differ at C-2)
Epimers
Because the substituents on the single bond between C-1 and C-2 can rotate freely, either the alpha or beta-anomer can be formed. This spontaneous change of configuration about C-1 is known as ________________, and occurs more rapidly when the reaction is catalyzed with an acid or base.
Mutarotation
Any monosaccharide with a hemiacetal ring is considered a ______________.
Reducing sugar
________________ refers to the rearrangement of bonds in a compound, usually by moving a hydrogen and forming a double bond.
Tautomerization
Because carbohydrates have hydroxyl groups, they are able to participate in reactions with carboxylic acids and carboxylic acid derivatives to form _________.
Esters
Disaccharides and polysaccharides form as a result of ____________ bonds between monosaccharides.
Glycosidic bonds
A polysaccharide composed entirely of glucose (or any other monosaccharide) is referred to as a ___________________.
Homopolysaccharide
A polymer made up of more than one type of monosaccharide is considered a ____________________.
Heteropolysaccharide
Cellulose, starch, and glycogen are all polysaccharides composed of the same monosaccharide, _______________.
D-glucose
_____________ is the main structural component of plants. The homopolysaccharide is a chain of beta-d-glucose molecules linked by beta-1,4 glycosidic bonds, with hydrogen bonds holding the actual polymer chains together for support.
Cellulose
____________ are polysaccharides that are more digestible by humans because they are linked via alpha-d-glucose-1,4 glycosidic bonds.
Starches
Amyloose is degraded by ______________ and ______________.
- Alpha-amylase
- Beta-amylase
_____________ cleaves amylose at the nonreducing end oof the polymer (the end with acetal) to yield maltose.
Beta-amylase
_____________ cleaves randomly along the chain to yield shorter polysaccharide chains, maltose and glucose.
Alpha-amylase
_____________ is a carbohydrate storage unit in animals. It has alpha-d-glucose-1,6 glycosidic bonds (approximately one for every 10 glucose molecules), which makes it a highly branched compound.
Glycogen
__________________ functions by cleaving glucose from glycogen from the nonreducing end of the glycogen branch and phosphorylating it, thereby producing glucose-1-phosphate, which plays an important role in metabolism.
Glycogen phosphorylase