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Yes, cyclic sugars are the favored form of aldohexoses in solution due to their stability and lower energy state compared to their open-chain forms. In aqueous environments, aldohexoses predominantly exist as cyclic hemiacetals, forming six-membered rings (pyranoses) through intramolecular reactions. This cyclic structure allows for more favorable interactions with water, making them more thermodynamically stable in solution.

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Related Questions

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 are the differences between the cyclic forms of ketose and aldose sugars?

The main difference between cyclic forms of ketose and aldose sugars is the location of the carbonyl group. In ketose sugars, the carbonyl group is located within the carbon chain, while in aldose sugars, the carbonyl group is located at the end of the carbon chain. This difference in carbonyl group location affects the overall structure and properties of the sugars.


Does cyclic lactose have a hemiacetal?

Cyclic lactose, which is a disaccharide composed of glucose and galactose, can form a hemiacetal. In its cyclic form, the anomeric carbon of one sugar unit reacts with a hydroxyl group of the other, resulting in a hemiacetal structure. This is characteristic of sugars that can exist in a cyclic form, where the carbonyl group reacts to form a new hydroxyl group at the anomeric carbon. Therefore, cyclic lactose does indeed contain a hemiacetal.


What are nonreducing sugars?

reducing sugars are those sugars which cannot donate electron and cannot reduce other solution


What is the indicator for simple sugars?

Benedict's Solution


What is an aldotetrose?

Aldotetrose is a type of sugar molecule that contains four carbon atoms. It is a carbohydrate and a type of monosaccharide. Aldotetroses are less common than other types of sugars like aldopentoses and aldohexoses.


What is the difference between iodine solution and Benedict's solution?

Iodine solution is used to test for the presence of starch, turning blue-black in the presence of starch. Benedict's solution is used to test for reducing sugars such as glucose, turning from blue to brick red in the presence of reducing sugars.


What does non-cyclic photophosphorylation produce?

Non-cyclic photophosphorylation, which occurs in the light-dependent reactions of photosynthesis, produces ATP and NADPH. These molecules serve as energy carriers that are used in the Calvin cycle to produce sugars.


Would glucose solution produce a positive Benedicts test?

No, Benedicts reagent will show positive results if the carbohydrate is a reducing sugar. You will know if it is positive if the sample will turn from blue to green then to orange when you are cooling the solution, which is the last step when you are performing the benedicts test for carbohydrates.


Does Benedict's solution reacts with proteins?

Benedict's solution reacts with reducing sugars, not proteins. It is commonly used in biochemical tests to detect the presence of reducing sugars such as glucose. Proteins do not typically react with Benedict's solution.


Why does the fehlings solution turn red?

The Fehling's solution turns red when it comes into contact with reducing sugars such as glucose. This color change occurs because the reducing sugars react with the copper ions in the Fehling's solution to form a red precipitate of copper(I) oxide. This is a characteristic test used to detect the presence of reducing sugars in a solution.


What is the reagent used to test for complex sugars?

benidict's solution