16. Please name the Glycosidic bond of the following disaccharides:HOCH₂HHHO\OH0HH OHH HOCH20-2HHHO/CH.OHCH₂OHOH H

A glycosidic bond is a covalent bond that links a carbohydrate molecule to another group, which may…

Answered: 16. Please name the Glycosidic bond of…

Biochemistry

9th Edition

ISBN:9781319114671

Author:Lubert Stryer, Jeremy M. Berg, John L. Tymoczko, Gregory J. Gatto Jr.

Publisher:Lubert Stryer, Jeremy M. Berg, John L. Tymoczko, Gregory J. Gatto Jr.

Chapter1: Biochemistry: An Evolving Science

Section: Chapter Questions

Problem 1P

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Similar questions

What type of glycosidic bond does the shown disaccharide have? но CH,OH O CH,OH O но. OH HO- OH wOH alpha (1 to 2) alpha (1 to 4) beta (1 to 2) beta (1 to 4)
Disaccharides are joined by glycosidic bonds formed between the anomeric carbon on one monosaccharide and a hydroxyl (-OH) group of another monosaccharide. Identify the types of linkages in each of the three disaccharides. Only place three of the linkages. НО. CH₂OH CH₂OH CH₂OH HO OH OH OH OH OH CH₂OH HO. НО OH OH 0 OH B12 al OH 4 OH 0 О CH₂OH Answer Bank al + B2 OH al + al OH B14 OH о OH OH
29. The two isomers that can form when glucose turns from an open chain to a closed ring is called: Epimers Anomers Enantiomers Diastereomers
1) Which of the following statement(s) regarding the ends of polysaccharides are true? All polysaccharides have at least one reducing end. Some polysaccharides may have no reducing end. Some polysaccharides may have no non-reducing ends. All polysaccharides have a N-glycosidic bond at their reducing ends. none of the above 2) The transformation of a monosaccharide into its ______ occurs easily and does not require the assistance of a catalyst. epimer anomer sugar alcohol diastereomer zwitterion
Although the first two carbons of fructose and glucose are identical in structure to DHAP and GADP (from glycolysis), DHAP and GADP equilibriate on their in solution to favor the ketone over the aldehyde, while fructose and glucose do not. Why? a)The larger size of the molecule sterically hinders the isomerization b)The larger sugars have more OH groups which hydrogen bond and disrupt isomerization c)The larger sugars cyclize, and there is no carbonyl to isomerize in the cyclic form d)The larger sugars cyclize, and in the cyclic form the hydrogen bonding is very strong e)The larger sugars are less soluble in water than the smaller sugars
12.
1. What feature of the structure of verbascose makes it indigestible?
16.
Could you explain step by step each answer and how to get there?
1. 2. List which carbohydrates are described as simple and which are complex? Briefly describe the general structures of monosaccharides, disaccharides, and polysaccharides (include the difference between starch and glycogen. Unbranched, occasional branching, and highly branched and how chemical structure effects function). Name the three monosaccharides considered to be important in nutrition, name the three disaccharides commonly found in foods and their component monosaccharides. Then name the foods these sugars are commonly found in (both mono and disaccharides).
1- Please refer to the Fisher representation of the 5 monosaccharides below: ÇH2OH CHO CHO CHO CHO H- H- он H- OH OH HO HO но- H- OH HO Но- H- -OH H- H- -OH HO- OH HO H- -OH H- -OH HO HO H- OH ČH2OH ČH2CH ČH2CH ČH2CH ČH2CH D-Fructose D-Glucose L-Glucose L-Idose D-Galactose 1a- Which one(s) of the above molecules belong(s) to the subcategory of aldohexoses? and which one(s) of these molecules belong(s) to the subcategory of ketohexoses? Briefly explain your response. 1b- Which one of the above molecules is an enantiomer of D-Glucose? and which one is an epimer of L-Ildose? Briefly explain your response.
Identify the D,L convention of the following monosaccharides

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