Exam 5 Review Topics (No metabolism) (1)
Page 1: Carbohydrate Structure
Aldose vs. Ketose
Aldose: Sugar with an aldehyde group at the end of the carbon chain.
Ketose: Sugar with a ketone group within the carbon chain.
Both are classified as monosaccharides.
Enantiomer Definition
Enantiomers: Molecular pairs that are mirror images but cannot be superimposed.
Example: D and L forms.
Diastereomer Definition
Diastereomers: Non-mirror image stereoisomers that differ at one or more stereocenters.
D and L Designations
D-sugars: Hydroxyl (-OH) group is on the right at the furthest chiral carbon.
L-sugars: Hydroxyl (-OH) group is on the left.
Anomer Definition
Anomers: Cyclic monosaccharides that differ at C-1 (aldoses) or C-2 (ketoses).
Example: α-D-Glucose and β-D-Glucose differ at the position of the -OH group.
Alpha and Beta Anomers
Alpha anomer: Hydroxyl group on anomeric carbon points opposite the -CH2OH on carbon five.
Beta anomer: Hydroxyl group on anomeric carbon points in the same direction as the -CH2OH on carbon five.
Page 2: Common Monosaccharides and Disaccharides
Common Monosaccharides
Glucose
Fructose
Galactose
Common Disaccharides
Formed through dehydration synthesis:
Sucrose
Maltose
Lactose
Glycosidic Bond Definition
Covalent bond linking carbohydrate molecules.
Connects hemiacetal group of one sugar to hydroxyl group of another molecule.
Page 3: Storage Molecules
Starch
Storage form of glucose in plants, composed of amylose and amylopectin.
Cellulose
Structural component of plant cell walls, serves as fiber for humans (indigestible).
Glycogen
Major storage form in animals, has a branched structure for quick energy release.
Page 4: Lipid Structure
Classes of Lipids
Fatty Acids: Saturated and Unsaturated.
Glycerides: Contain glycerol.
Phospholipids: Include phosphoglycerides and sphingolipids.
Glycolipids
Steroids: Cholesterol.
Complex Lipids: Lipoproteins.
General Structure of a Lipid
Consists of a glycerol backbone and three fatty acid chains connected via ester bonds.
General Structure of Triglyceride
Three fatty acids attached to a glycerol.
Page 5: Fatty Acids
Unsaturated Fatty Acids
cis isomer is most prevalent in nature; results in a bent chain.
Trans isomer: Unnatural, linear chain.
Saturated Fatty Acid Definition
No double bonds; solid at room temperature.
Structure: CH3 (CH2)n COOH (where n = even number).
Page 6: Characteristics of Unsaturated Fatty Acids
Unsaturated Fatty Acid Definition
At least one double bond; typically liquid at room temperature.
Types:
Monounsaturated: One double bond.
Polyunsaturated: Multiple double bonds.
Ester Bond Definition
Formed between fatty acid and alcohol; releases a water molecule.
Esterification: Reaction between carboxyl and hydroxyl groups.
Naming Omega Fatty Acids
Based on first double bond position counted from omega carbon.
Omega-3: Found in fish and plants.
Omega-6: Found in vegetable oils.
Page 7: Physical Properties of Triglycerides and Phospholipids
Physical Properties of Triglycerides
Colorless, non-polar, hydrophobic; appear as oils (liquid) or fats (solid).
Physical Properties of Oils
Oils generally have higher proportions of unsaturated fatty acids.
Saturated acids fit together easily; unsaturated have kinks, preventing solidification.
Hydrogenation Reaction
Addition of hydrogen to double bonds; converts oils to solid fats.
Example: Margarine is partially hydrogenated.
Structure of Phospholipids
Two fatty acids attached to glycerol; phosphate group on the third carbon.
Page 8: Sphingolipids and Cholesterol
Structure of Sphingolipids
Essential for cell membranes; based on sphingosine, which contains an amino group and an unsaturated hydrocarbon chain.
Function of Cholesterol
Provides rigidity to animal cell membranes.
Types of Lipoproteins
Macromolecular structures made from proteins and lipids, include enzymes, transporters, structural proteins, etc.