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In most of the cases glycosidic linkage is formed between (a) \(\left(1 \longrightarrow 4^{\prime}\right)\) (b) \(\left(4 \longrightarrow 4^{\prime}\right)\) (c) \(\left(2 \longrightarrow 2^{\prime}\right)\) (d) \(\left(1 \longrightarrow 3^{\prime}\right)\)

Short Answer

Expert verified
In most cases, glycosidic linkage is formed between 1 → 4.

Step by step solution

01

Understanding Glycosidic Linkage

Glycosidic linkage is a covalent bond that joins a carbohydrate molecule to another group, which can be another carbohydrate. This type of bond is essential in the formation of disaccharides, oligosaccharides, and polysaccharides.
02

Identifying Common Glycosidic Linkages

The most common glycosidic linkage in carbohydrates, especially disaccharides, is the 1 → 4 linkage. This is often seen in structures like maltose, where one glucose molecule's C1 carbon is linked to another glucose's C4 carbon.
03

Analyzing The Given Options

Analyze the given options to identify which one typically represents the most common glycosidic linkage: (a) 1 → 4, (b) 4 → 4, (c) 2 → 2, and (d) 1 → 3. From Step 2, we found that 1 → 4 is the typical linkage in common carbohydrates.

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Key Concepts

These are the key concepts you need to understand to accurately answer the question.

Covalent Bond
A covalent bond is a strong chemical connection between two atoms that share a pair of electrons. This sharing allows each atom to achieve a stable outer electron shell, similar to what noble gases have. In the context of carbohydrates, covalent bonds are crucial as they form the backbone of many structures.
For instance, glycosidic linkages, which are a type of covalent bond, bind sugar molecules together to create complex carbohydrates.
  • Glycosidic linkages connect monosaccharides (simple sugars) to form disaccharides (like sucrose and lactose) and further, complex carbohydrates.
  • Covalent bonds ensure stability and strength in carbohydrate structures, making these molecules less likely to break apart in biological systems.
Understanding covalent bonds helps us appreciate how carbohydrates function in energy storage and structural support in cells.
Disaccharides
Disaccharides are carbohydrates that consist of two sugar molecules bonded together via a glycosidic linkage. These small sugar chains serve as an essential energy source in our diet.
Some common disaccharides include:
  • Sucrose - made from glucose and fructose; it is found in many plants and a major component of table sugar.
  • Lactose - consists of glucose and galactose; it is the sugar found in milk.
  • Maltose - formed by linking two glucose molecules; it appears during the digestion of starch.
The glycosidic bonds in disaccharides can be hydrolyzed (broken down by water) during digestion, releasing simple sugars that the body can easily absorb and use for energy. This process is vital for utilizing carbohydrates as nutrients.
Carbohydrate Structure
Carbohydrates are organic molecules composed of carbon, hydrogen, and oxygen. They are classified based on the number of sugar units they contain: monosaccharides (one sugar unit), disaccharides (two sugar units), oligosaccharides (3-10 sugar units), and polysaccharides (more than ten sugar units).
The complex structure of carbohydrates is largely due to the variety of ways they can connect through glycosidic linkages.
  • Monosaccharides like glucose are the simplest form and can combine to form larger structures.
  • Through glycosidic bonding, these sugars link together into more complex carbohydrates, such as starch and cellulose.
  • The molecular structure can vary greatly within carbohydrates due to the variety of possible linkages, allowing for a vast range of functions, from energy storage to providing structural integrity in plant cell walls.
Recognizing and understanding the structure of carbohydrates helps in grasping their biological significance and functionality in living organisms.

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Most popular questions from this chapter

Hydrolysis of lactose with dilute acid yields (a) equimolar mixture of D-glucose and D-glucose (b) equimolar mixture of D-glucose and Dgalactose (c) equimolar mixture of D-glucose and D-fructose (d) equimolar mixture of D-galactose and Dgala-ctose

Which of the following Aminoacids can be used in the prepration of dipeptide? (a) CC(N)C(=O)O (b) \(\mathrm{H}_{2} \mathrm{~N}-\mathrm{CH}_{2}-\mathrm{CH}_{2}-\mathrm{CH}_{2}-\mathrm{COOH}\) (c) CC(N)CC(=O)O (d) NCC(=O)O

Consider the following statements about carbohydrates: 1\. Bromine water can be used to differentiate an aldose from a ketose 2\. All monosaccharides, whether aldose or ketose, are reducing sugars 3\. Osazone formation destroys the configuration about C-2 of an aldose, but does not affect the configuration of the rest of the molecule 4\. A pair of diastereomeric aldoses which differ only in configuration about \(\mathrm{C}-2\) is termed as pair of anomers Which of the above statements are correct? (a) 1 and 4 (b) 2 and 4 (c) 1,2 and 3 (d) 2,3 and 4

Consider the following statements about sucrose. 1\. hydrolysis of sucrose with dilute acid yields an equimolar mixture of D-glucose and D-fructose 2\. acid hydrolysis of sucrose is accompanied by a change in optical rotation 3\. in sucrose, the glycosidic linkage is between C-1 of glucose and \(\mathrm{C}-2\) of fructose 4\. aqueous solution of sucrose exhibits mutarotation Which of the statements are correct? (a) 1 and 2 only (b) 2 and 3 only (c) 1,2 and 3 (d) 1,3 and 4

Choose the correct relationship for \(\alpha\)-D-glucose (A) and \(\beta\)-D-glucose (B). (a) \(\mathrm{A}\) and \(\mathrm{B}\) are crystal modification (b) A and B are epimers (c) A is an aldose and \(\mathrm{B}\) is a ketose (d) A is a pyranose sugar and \(\mathrm{B}\) is a furanose sugar

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