Skip to content

Dehydration Synthesis: The Common Process When Monosaccharides are Combined to Form Disaccharides

2 min read

In a biological world powered by macromolecules, the process of building complex molecules from simpler ones is fundamental. When monosaccharides are combined to form disaccharides, the common chemical process involved is dehydration synthesis. This reaction, also known as a condensation reaction, is critical for forming the covalent bonds that link these sugar units together.

Quick Summary

This article explains how monosaccharides are joined to create disaccharides through the chemical process of dehydration synthesis, which releases a water molecule. It details the formation of the glycosidic bond, provides examples with common sugars like sucrose and lactose, and contrasts this constructive process with the opposite, hydrolytic reaction.

Key Points

  • Process Name: Dehydration synthesis, also known as a condensation reaction.

  • Water Removal: A molecule of water is removed as a byproduct.

  • Bond Formation: A glycosidic bond links the monosaccharides.

  • Examples: Sucrose, lactose, and maltose are formed this way.

  • Energy Required: The process needs energy input.

  • Reverse Process: Hydrolysis breaks down disaccharides using water.

In This Article

Understanding the Dehydration Synthesis Reaction

Dehydration synthesis is a type of condensation reaction where two molecules are joined together to form a larger molecule with the loss of a water molecule. The name 'dehydration' signifies the removal of water, while 'synthesis' means to build. This process links monosaccharides to create disaccharides and polysaccharides. The reaction involves the removal of a hydroxyl group ($-OH$) from one monosaccharide and a hydrogen atom ($-H$) from another, which combine to form a water molecule ($H_2O$) released as a byproduct. A covalent bond then forms between the two sugar units.

The Formation of the Glycosidic Bond

The covalent bond formed between two monosaccharides during dehydration synthesis is called a glycosidic bond or glycosidic linkage. This bond forms between the anomeric carbon of one sugar and a hydroxyl group of another. The type of glycosidic bond (alpha or beta) influences the properties of the resulting disaccharide and its biological implications, such as digestibility.

Examples of Disaccharide Formation via Dehydration Synthesis

Common disaccharides formed by this process include:

  • Sucrose: Glucose + Fructose, linked by an $α(1 o 2)$ glycosidic bond with the release of water.
  • Lactose: Glucose + Galactose, joined by a $β(1 o 4)$ glycosidic bond after water removal.
  • Maltose: Two glucose molecules linked by an $α(1 o 4)$ glycosidic bond through dehydration.

Dehydration Synthesis vs. Hydrolysis

Hydrolysis is the reverse of dehydration synthesis. It breaks down larger molecules by adding water, whereas dehydration synthesis builds molecules by removing water.

Feature Dehydration Synthesis Hydrolysis
Function Builds polymers from monomers Breaks polymers into monomers
Water Involvement Water is removed (byproduct) Water is added (reactant)
Bond Formation/Breakage Forms new covalent bonds Breaks covalent bonds
Energy Requirement Requires energy input Releases energy
Example Monosaccharides combine to form disaccharides Disaccharides break down into monosaccharides

Digestion uses hydrolysis to break down disaccharides and polysaccharides into monosaccharides for absorption and energy.

Conclusion

Combining monosaccharides to form disaccharides occurs through dehydration synthesis, a reaction that removes water to create a glycosidic bond between sugar units. This process is fundamental for creating larger carbohydrates like sucrose, lactose, and maltose. Understanding dehydration synthesis is key to comprehending how organisms synthesize and use carbohydrates.

Frequently Asked Questions

What are monosaccharides? Monosaccharides are the simplest sugars like glucose, fructose, and galactose, serving as building blocks for larger carbohydrates.

What is the byproduct of dehydration synthesis? The byproduct is a water molecule ($H_2O$), released when monomers join.

Is dehydration synthesis the same as a condensation reaction? Yes, it's a type of condensation reaction where water is released.

What is the reverse reaction of dehydration synthesis? Hydrolysis is the reverse, using water to break bonds in larger molecules.

What is a glycosidic bond? The covalent bond formed between two monosaccharides during dehydration synthesis is a glycosidic bond.

How does the type of glycosidic bond matter? The type of glycosidic bond affects the disaccharide's shape and biological function, including digestibility.

What enzyme helps break down disaccharides? Disaccharidases, like lactase, use hydrolysis to break down disaccharides.

Frequently Asked Questions

Dehydration synthesis is a chemical reaction in which two smaller molecules are joined to form a larger molecule with the loss of a water molecule.

The covalent bond that connects two monosaccharides to form a disaccharide is called a glycosidic bond or glycosidic linkage.

Yes, sucrose is formed from one molecule of glucose and one molecule of fructose through a dehydration synthesis reaction.

Dehydration synthesis is a constructive process that removes water to form bonds, while hydrolysis is a breakdown process that adds water to break bonds.

During dehydration synthesis, a hydroxyl group ($-OH$) from one monosaccharide and a hydrogen atom ($-H$) from another are removed to form a water molecule, which is released.

Common disaccharides formed by dehydration synthesis include sucrose (glucose + fructose), lactose (glucose + galactose), and maltose (glucose + glucose).

Specific enzymes, such as sucrase, lactase, or maltase, catalyze (speed up) the dehydration synthesis and hydrolysis reactions in living organisms.

The alpha and beta distinction is crucial because it determines the overall shape and biological function of the disaccharide. For example, humans can digest starches with alpha bonds but not cellulose with beta bonds.

References

  1. 1
  2. 2
  3. 3
  4. 4

Medical Disclaimer

This content is for informational purposes only and should not replace professional medical advice.