Biomolecules
REDUCING AND NON-REDUCING SUGARS
- A reducing sugar is a sugar that can reduce other substances through a chemical reaction
- It has a free aldehyde or ketone functional group
- Examples of reducing sugars include glucose, fructose, and maltose
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- Non-reducing sugars do not have a free aldehyde or ketone group
- They cannot undergo the same chemical reaction to reduce other substances
- Examples of non-reducing sugars include sucrose and lactose
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Examples of Reducing Sugars
- Glucose (C6H12O6)
- Fructose (C6H12O6)
- Maltose (C12H22O11)
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Examples of Non-Reducing Sugars
- Sucrose (C12H22O11)
- Lactose (C12H22O11)
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Reducing Sugar Reactions
- Reducing sugars can undergo oxidation reactions
- For example, glucose can be oxidized to form gluconic acid
- This oxidation reaction involves the reduction of another substance, such as a metal ion
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Non-Reducing Sugar Reactions
- Non-reducing sugars, such as sucrose, do not undergo oxidation reactions
- They cannot be directly oxidized to form acids or alcohols
- However, they can be hydrolyzed to form their constituent monosaccharides
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Hydrolysis of Sucrose
- Sucrose can be hydrolyzed to form glucose and fructose
- This reaction is catalyzed by the enzyme sucrase
- The hydrolysis of sucrose is a reversible reaction
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Sucrose Hydrolysis Equation
Sucrose + H2O → Glucose + Fructose
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Importance of Reducing and Non-Reducing Sugars
- Reducing sugars play a crucial role in various biological processes
- They can be used as a source of energy by organisms
- Non-reducing sugars, such as sucrose, are important in transportation and storage of energy in plants
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Summary
- Reducing sugars have a free aldehyde or ketone group and can undergo oxidation reactions
- Non-reducing sugars do not have a free aldehyde or ketone group and cannot undergo oxidation reactions
- Examples of reducing sugars include glucose, fructose, and maltose
- Examples of non-reducing sugars include sucrose and lactose
Note: Please continue creating slides 11 onwards.
Types of Carbohydrates
Monosaccharides
- Simplest form of carbohydrates
- Cannot be hydrolyzed into smaller units
- Examples: glucose, fructose, galactose
Disaccharides
- Two monosaccharides joined together by a glycosidic bond
- Can be hydrolyzed into two monosaccharides
- Examples: sucrose, lactose, maltose
Polysaccharides
- Complex carbohydrates made up of many monosaccharide units
- Can be hydrolyzed into multiple monosaccharides
- Examples: starch, cellulose, glycogen
Structure of Carbohydrates
- Monosaccharides can exist in linear form
- Formed by a chain of carbon atoms with functional groups attached
Ring Structure
- Monosaccharides can also exist in ring structure
- In ring form, the carbonyl group reacts with an alcohol group to form a hemiacetal or hemiketal
- In ring structure, monosaccharides can exist in alpha (α) or beta (β) form
- Differ in the orientation of the hydroxyl group attached to the anomeric carbon atom
- Glucose: α-glucose and β-glucose
- Fructose: α-fructose and β-fructose
Functions of Carbohydrates
Energy Source
- Carbohydrates are the primary source of energy for living organisms
- Glucose is the most commonly used carbohydrate for energy production
Structural Roles
- Carbohydrates play a key structural role in cells and tissues
- Examples include cellulose in plant cell walls and chitin in the exoskeleton of insects
Cell-Cell Communication
- Carbohydrates on the surface of cells play a role in cell-cell recognition and communication
- They help in immune responses, tissue development, and cell signaling
Storage of Energy
- Carbohydrates are stored in the form of glycogen in animals and starch in plants
- These storage forms can be broken down to release glucose when needed
Carbohydrate Derivatives
Glycosides
- Glycosides are formed by replacing the hydroxyl group of a carbohydrate with another functional group
- Common examples include disaccharides like sucrose and lactose
Glycoproteins
- Glycoproteins are proteins that have carbohydrates attached to them
- They play important roles in cell recognition, immune response, and cell signaling
Glycolipids
- Glycolipids are lipids that have carbohydrates attached to them
- Found in cell membranes and play roles in cell-cell recognition and signaling
Nucleotides and Nucleic Acids
- Nucleotides, the building blocks of nucleic acids, contain a carbohydrate (ribose or deoxyribose)
- Nucleic acids, such as DNA and RNA, store and transmit genetic information
Carbohydrates in Daily Life
Food and Nutrition
- Carbohydrates are an important part of our diet
- They provide energy and are found in foods like fruits, vegetables, grains, and dairy products
Food Additives
- Carbohydrates are used as food additives for various purposes
- Examples include stabilizers, thickeners, and sweeteners
Industrial Uses
- Carbohydrates have industrial applications, such as in the production of biofuels and bioplastics
- They are also used in fermentation processes to produce ethanol and other chemicals
Pharmaceutical Industry
- Carbohydrates play a role in drug delivery and formulation in the pharmaceutical industry
- They can be used as excipients, stabilizers, or carriers for drug molecules
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# Biomolecules - REDUCING AND NON-REDUCING SUGARS
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- A reducing sugar is a sugar that can reduce other substances through a chemical reaction
- It has a free aldehyde or ketone functional group
- Examples include glucose, fructose, and maltose
----
- Non-reducing sugars do not have a free aldehyde or ketone group
- They cannot undergo the same chemical reaction to reduce other substances
- Examples include sucrose and lactose
----
### Examples of Reducing Sugars
- Glucose (C6H12O6)
- Fructose (C6H12O6)
- Maltose (C12H22O11)
----
### Examples of Non-Reducing Sugars
- Sucrose (C12H22O11)
- Lactose (C12H22O11)
----
## Reducing Sugar Reactions
- Reducing sugars can undergo oxidation reactions
- For example, glucose can be oxidized to form gluconic acid
- This oxidation reaction involves the reduction of another substance, such as a metal ion
----
## Non-Reducing Sugar Reactions
- Non-reducing sugars, such as sucrose, do not undergo oxidation reactions
- They cannot be directly oxidized to form acids or alcohols
- However, they can be hydrolyzed to form their constituent monosaccharides
----
### Hydrolysis of Sucrose
- Sucrose can be hydrolyzed to form glucose and fructose
- This reaction is catalyzed by the enzyme sucrase
- The hydrolysis of sucrose is a reversible reaction
----
### Sucrose Hydrolysis Equation
- Sucrose + H2O → Glucose + Fructose
----
## Importance of Reducing and Non-Reducing Sugars
- Reducing sugars play a crucial role in various biological processes
- They can be used as a source of energy by organisms
- Non-reducing sugars, such as sucrose, are important in transportation and storage of energy in plants
----
## Summary
- Reducing sugars have a free aldehyde or ketone group and can undergo oxidation reactions
- Non-reducing sugars do not have a free aldehyde or ketone group and cannot undergo oxidation reactions
- Examples of reducing sugars include glucose, fructose, and maltose
- Examples of non-reducing sugars include sucrose and lactose
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