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All sugars are well soluble because they all have many possibillities for hydrogen bonds (on -C-OH- and -C-O-C- groups), many of these polar groups are pointing towards the outside of pyrose or furanose ring stucture.

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13y ago
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Both D-glucose and L-glucose are very soluble in water because of the presence of multiple hydroxyl (OH) groups that can form hydrogen bonds with water molecules, making them able to dissolve easily. Solubility is not significantly affected by the stereochemistry of the glucose molecule.

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Q: What is the reason for D glucose and L glucose solubility?
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What glucose stereoisomers are found in nature?

The D-glucose and L-glucose stereoisomers are found in nature. D-glucose is the common form of glucose found in biological systems, whereas L-glucose is less common and typically not metabolized by most organisms.


Why d-glucose is called levose?

D-glucose is not typically referred to as "levose." This term is commonly used for L-glucose, a stereoisomer of D-glucose where the hydroxyl (-OH) group on the asymmetric carbon farthest from the carbonyl group (-CHO) points to the left. D-glucose, on the other hand, is the naturally occurring form of glucose where the hydroxyl group on this chiral carbon points to the right.


D-glucose and l-glucose are are examples of what?

D-glucose and L-glucose are examples of enantiomers, which are non-superimposable mirror image molecules. They have the same chemical formula and bonds but differ in their spatial arrangement of atoms.


D glucose and l glucose are examples of?

According to the Fischer projection formula, they are enantiomers.


What is the difference between Dextrose and Glucose polymer?

Dextrose is a simple sugar and a form of glucose, while glucose polymer is a complex carbohydrate made up of multiple glucose molecules linked together. Glucose polymer is slower to be broken down and absorbed by the body compared to dextrose, providing a more sustained release of energy.


Can sucrose hydrolysis result L-glucose?

No, sucrose hydrolysis will not result in L-glucose. Sucrose is made up of glucose and fructose, but the hydrolysis of sucrose produces equal parts of glucose and fructose in their D form, not L-glucose.


What is stereoisomers of the aldohexoses?

The aldohexoses have 16 stereoisomers: 8 D-sugars and 8 L-sugars. The D-sugars include D-glucose, D-galactose, and D-mannose, while the L-sugars include L-glucose, L-galactose, and L-mannose. These stereoisomers differ in the arrangement of hydroxyl groups around the chiral carbons.


What is the solubility of Na-CI at 20 degrees Celsius?

The solubility of sodium chloride at 20 0C is 360,9 g/L.


Draw and name the enantiomer of D-glucose?

The enantiomer of D-glucose is L-glucose. It has the same molecular formula and structure as D-glucose but differs in the spatial arrangement of atoms, specifically at the chiral carbon (C5) where the hydroxyl group is oriented differently.


What is the different between D-glucose and L-glucose?

You can see in the above image the only difference is the position of the hydroxyl group (OH) on the carbon chain. They are mirror images of the other but they do not overlap. L-Glucose has to be made in a lab, whereas D-Glucose is naturally occurring. I've written an answer to the following question that might give you some more insight to the pathways involved.


What is the difference between D-glucose and L-glucose?

You can see in the above image the only difference is the position of the hydroxyl group (OH) on the carbon chain. They are mirror images of the other but they do not overlap. L-Glucose has to be made in a lab, whereas D-Glucose is naturally occurring. I've written an answer to the following question that might give you some more insight to the pathways involved.


What can the structure of glucose be classified as A. L-monosaccharide B. Ketose C. Disaccharide D. D-monosaccharide E. Furanose?

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