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Organism rely on the oxidation of complex organic compounds to obtain energy.
True
Three general types of complex organic compounds to obtain energy
Carbohydrates
Amino acids
Lipids
The primary source of energy for brain, erythrocytes, and retinal cells in humans.
Carbohydrates
The major food source and energy supply for the body and are stored primarily in the liver and muscle as GLYCOGEN.
Carbohydrates
The two split into a disease related to carbohydrates.
Hyperglycemia
Hypoglycemia
A compound containing C, H, O
Carbohydrates
Disease states involving carbohydrates are split into two groups?
hyperglycemia (which can lead to diabetes mellitus)
and hypoglycemia.
are compounds containing C, H, and O.
Carbohydrates
The general formula for a carbohydrate is
Cx(H2O)y
All carbohydrates contain _____ and _______ functional groups.
C=O and –OH functional groups.
The classification of carbohydrates is based on four structural properties:
(1) the size of the base carbon chain,
(2) the location of the CO function group,
(3) the number of sugar units,
and (4) the stereochemistry of the compound.
based on the number of carbons in the molecule. For example, trioses contain how many carbons?
three carbons
tetroses contain
four carbons
pentoses
5 carbons
hexoses
6 carbon
In actual practice, the smallest carbohydrate is
Glyceraldehyde - a three carbon compound.
What are the hydrates derivate of carbohydrates?
Aldehyde and Ketone derivatives based on the location of the CO FUNCTIONAL GROUP.
The two forms of carbohydrates
Aldose
Ketose
has a terminal carbonyl group (O=CH–) called an aldehyde group
Aldose form
has a carbonyl group (O=C) in the middle linked to two other
carbon atoms (called a ketone group).
Ketose Form.

Ketone

Aldehyde
It has the aldehyde or ketone at the top of the drawing.
The compound can be represented as a straight chain or might be linked to show a representation of the cyclic, hemiacetal form.
The Fisher projection
represents the compound in the cyclic form that is more representative of
the actual structure. This structure is formed when the functional (carbonyl) group (ketone or aldehyde) reacts with an alcohol group on the same sugar to form a ring called either a hemiketal or a hemiacetal ring,
Haworth projection
four different groups areattached to the carbon atoms.
Asymmetric (chiral)
This allows for various spatial arrangements around each
asymmetric carbon (also called stereogenic centers) forming molecules called
Stereoisomers.
have the same order and types of bonds but different spatial arrangements and different properties
Stereoisomers
A monosaccharide is assigned to the D or the L series according to the configuration at the highest numbered asymmetric carbon.
In a Fischer projection, the OH group on the configurational carbon is on the left. Which series is the sugar in?
L - Series
A sugar has 3 chiral carbons. What is the maximum number of stereoisomers?
8
What is the relationship between D-glyceraldehyde and L-glyceraldehyde?
Most naturally occurring sugars in humans are
in the d-form or l-form?
D - Form.
When they split, one molecule of water is consumed to form the individual
sugar compounds. This reaction is called
Hydrolysis
This chaining of sugars relies on the formation of bridges of oxygen atoms.
Glycoside Bonds
are simple sugars that cannot be hydrolyzed to a simpler
form; there is one sugar molecule.
Monosaccharides
The most
common hexose monosaccharides include
Glucose, fructose, and galactose.
Are formed when two monosaccharide units are joined by a glycosidic
linkage.
Disaccharides
On hydrolysis, disaccharides will be split into two monosaccharides by
Disaccharides enzyme (example: lactase) located on the Microvilli on the intestine.
The most common disaccharides are:
maltose (comprising two d-glucose molecules in a 1 → 4 linkage), lactose, and sucrose
chaining of 3 to 10 sugar units
Oligosaccharides
formed by the linkage of many monosaccharide units. 10 or more sugar units.
Oligosaccharides
an enzyme found in saliva and in the stomach,
hydrolyzes starch to disaccharides in the duodenum.
Amylase
he most common polysaccharides are starch (plant based glucose molecules) and glycogen (animal based glucose molecules)
starch (plant based glucose molecules) and glycogen (animal based glucose molecules)
these carbohydrates can reduce other compounds while they themselves are oxidized
Reducing substances
T o be a reducing substance, the carbohydrate
must contain an
active (available) ketone or an aldehyde group
Carbohydrates can form glycosidic bonds with other carbohydrates and with
noncarbohydrates.
n
forming the glycosidic bond, an ______ is generated on one sugar (at carbon 1) in place of the
hemiacetal.
Acetal
Examples of common-reducing sugars
Glucose, maltose, fructose, lactose, and galactose.
If a glycosidic bond is formed with the anomeric carbon on the
other carbohydrate, the resulting compound is
no longer a reducing substance.
Nonreducing
carbohydrates do not have an active ketone or aldehyde group and therefore will not reduce
other compounds.
The most common nonreducing sugar
Sucrose - table sugar.