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Understanding Carbohydrates and Their Functions
Aug 14, 2024
Lecture on Carbohydrates
Introduction to Carbohydrates
Definition
: Carbohydrates are chemical compounds made up of carbon atoms that are fully hydrated (carbo = carbon, hydrate = water).
General Formula
: C_n(H2O)_n (n = number of carbon atoms).
Ratio
: 1:2:1 ratio of carbon, hydrogen, and oxygen._
Types of Carbohydrates
Monosaccharides
: Single carbohydrate molecules (simple sugars).
Derived from the Greek word for sugar, saccharide.
Polysaccharides
: Multiple carbohydrate molecules linked together (e.g., cellulose forms the structural backbone of plant cell walls).
Notable monosaccharides include glucose and ribose.
Functionality of Carbohydrates
Energy Source
: Glucose is the main energy source for metabolism in the body.
Structural Role
: Cellulose provides structural rigidity in plant cell walls.
Genetic Support
: Ribose is a component of RNA, supporting genetic transcription.
Naming Conventions
Suffix
: -ose indicates a sugar (e.g., glucose, cellulose, ribose).
Number of Carbons
:
Tri = 3 (triose)
Tetra = 4 (tetrose)
Penta = 5 (pentose)
Hexa = 6 (hexose)
Examples
Glyceraldehyde
: A simple carbohydrate with three carbons (triose).
Glucose
: A six-carbon carbohydrate (hexose) with an aldehyde functional group (aldohexose).
Fructose
: Another six-carbon carbohydrate (hexose) but with a ketone functional group (ketohexose).
Functional Groups
Aldehyde vs Ketone
: Determines the second naming prefix.
Aldohexose (e.g., glucose has an aldehyde group).
Ketohexose (e.g., fructose has a ketone group).
Stereochemistry
Fisher Projection
: Used to determine the highest numbered chiral center.
R (Right) or D (Dexter) configuration: Hydroxyl group on the right.
L (Left) configuration: Hydroxyl group on the left.
Examples
:
D-Glucose: A D-aldohexose due to the right-side placement of the hydroxyl group.
D-Fructose: A D-ketohexose with the hydroxyl group on the right.
Additional Learning Resources
Recommended video on Fisher projections from Khan Academy to better understand stereochemistry in carbohydrates.
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