Chapter 10 Flashcards
What are monosaccharides?
- The simplest form of carbohydrates
- Composed of a single aldehyde or ketose group that has two or more hydroxyl groups
The smallest monosaccharides (composed of three carbons) are…
- Dihydroxyacetone
- D-glyceraldehyde
- L-Glyceraldehyde
Ketose
- Is a monosaccaride
- Dihydroxyacetone is an example of a ketose because it contains a keto group (C=O)
- The ketone group as its most oxidized atom
Aldose
- Is a monosaccaride
- Glyceraldehyde is an example of an aldose because it contains an aldehyde group (C=O and H)
- C-1 atom contains aldehyde group
Dihydroxyacetone and Glyceraldehyde are referred to as _______ because they have three carbon atoms
Trioses
Ethryose is referred to as _____ because it has four carbon atoms
Tetrose
Ribose, ribulose, deoxyribose, xylose, xyulose are examples of ______ because they have five carbon atoms
Pentose
Glucose, mannose, galactose, fructose are examples of ______ because they have six carbon atoms
Hexose
Sedoheptulose is referred to as a _______ because it has seven carbon atoms
Heptose
If a monosaccharide has eight carbon atoms, it is referred to as ________
Octose
Neuraminic acid is an example of a ________ because it has nine carbon atoms
Nonose
Common monosaccharides will generally be in _______ form and _______ configuration
D-form; D-configuration
D-configuration is when those whose asymmetrical carbon atoms has a hydroxyl group projecting to the _______, whereas L-configurations are those whose whose asymmetrical carbon atoms has a hydroxyl group projecting to the _______
right; left
Common 5-carbon sugars are include:
- D-ribose (aldose)
- D-oxyribose (aldose)
Both above are sugar moieties in nucleic acids DNA and RNA
Common 6-carbon sugars are include:
- D-glucose (aldose)
- D-mannose (aldose)
- D-galactose (aldose)
- D-fructose (ketose)
Constitutional atoms
have identical molecular formulas, but differ in the order of the attachment of the atoms
What are stereoisomers?
Where atoms are connected in the same order but differ in spatial arrangement
What are enantiomers?
- A Stereoisomer
- Pair of molecules, each with one or more chiral centers, where atoms are mirrors of each other
What are chiral centers?
A carbon that has 4 unique atoms or groups attached to it
What are diastereoisomers?
- A Stereoisomer
- Pair of molecules, each w/ more than one asymmetric centre
- Atoms have opposite configurations; NOT mirrors of each other
What are epimers?
- A Diastereoisomers
- Pair of molecules (with more than one asymmetric centre) differing at a SINGLE asymmetric centre
What are anomers?
- A Diastereoisomers
- Differ at the new asymmetric anomeric carbon that’s formed due to the formation of a hemiacetal or hemiketal
A hemiacetal is formed when an ________ reacts with an alcohol
aldehyde
A hemiketal is formed when an ________ reacts with an alcohol
ketone
A pyranose is formed when the ______ in open chain form reacts with the _______, which forms an intramolecular hemiacetal
C1 aldehyde; C-5 hydroxyl,
A furnose is formed when the ________ in open-chain form reacts with the _______, which forms a five-membered cyclic hemiketal
C-2 keto group; C-5 hydroxyl group
This can also form if the C-2 keto group reacts with the C-6 hydroxyl group to form six-membered cyclic hemiketal
True or False: Reducing sugars don’t react with solutions of cupric ions while non-reducing sugars do
False: Reducing sugars react with solutions of cupric ions while non-reducing sugars do not
As a reducing sugar, glucose can react with _______ to form _______, also known as hemoglobin A1C. In this case, the hemoglobin is ______ functional
hemoglobin; glycosylated hemoglobin; fully
Determining and quantifying the amount of A1C hemoglobin in blood allows for what?
It allows for long-term monitoring and control of blood glucose levels, which is an important consideration for diabetics who have an increased rate of glycosylation due to increased blood glucose concentrations