DRAW ON PAPER PLEASE - Amylose is a linear polymer of several thousand glucose units linked by (14) glycosidicbonds. Assume that a molecule of amylose is treated with dimethyl sulfate, which adds a methyl group to all freehydroxyl groups. Then, the -amylose is hydrolyzed to release all its monosaccharide units. How many different chemicalproducts are there (ignoring stereoisomers)? Draw the most abundant product (Haworth projection). i will rate if youdraw on paper thanks

Amylose is a polysaccharide. It is made up of -D-glucose residues linked via (14) glycosidic linkage…

Answered: DRAW ON PAPER PLEASE - Amylose is a…

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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Н. Based on what you know about the classification and structure of galactose, HO- what possible results would you obtain if H- ОН Но- H- H. но- you were to perform the following tests? (+) negative (-) and explain in one sentence) ОН (indicate whether positive or ČH2OH Test Result Explanation Benedict's Barfoed's Seliwanoff's lodine Test I I
1,2-dioleoyl-3-myristyl-sn-glycerolsn-16:0-12:0-16:0LLnO Consider the TAGS abovea. Which is most prone to lipid oxidation? Explain.b. Which has the highest melting point? Explain.c. Which will most likely convert fastest to the most stable polymorphic form. Explain.
Fill in ..... (1) the complete systematic names for sugars A, B and C (remember to you pyranosyl or furanosyl because these are not the terminal sugar). (2) The appropriate descriptor of the glycosidic bonds where appropriate/necessary. (3) Draw the missing sugars as indicated onto the given diagram. HO OH GED A HO OH a-L-psicofuranose (1➜6)- (1➜4)- a-D-idopyranose HO OH B OH OH OH OH SUGAR A SUGAR B SUGAR C
10. Procaine is known to undergo faster metabolic hydrolysis than procainamide. Give explanation. -NET2 -NEt2 HN H2N- H2N- Procainamide Procaine 11. In phase 2 metabolic transformation chloramphenicol the primary alcohol is converted to a glucuronide conjugate. Draw chemical structure of the product. Provide the name of enzyme that catalyze this metabolic reaction. он ? CHCI2 O2N- но
If the glucose molecule was labeled with 14C at the C-3, which carbon atom in pyruvate would you expect to find labeled? Select the structure of pyruvate showing its appropriate structure at pH 7.4. The structure should have a carbon highlighted in green and bold that corresponds to the original 14C labeled C-3 of glucose. H3C-C-C-OH H3C-C-C -O H3C-C-c-OH H3C C-C- H3C-C-C- H3C-C HO-
b. Identify (name) each of the following two monosaccharides A and B. НО ОН ОН По A ОН -ОН но- Но Но ОН в ОН c. The disaccharide lactose is built up by one D-galacto-and one D-gluco monosaccharide unit. Draw L-galactose in the Fischer projection (open) form and in its most stable pyranose ring conformation form and determine if the latter is a ¹C4 or a 4C₁ conformation.
Which of the following is true regarding Glycogen Linear homopolysaccharide O Contains beta-1 to 4 bonds O It has alph-helical structure O Energy storage heteropolysaccharide O Branched heteropolysaccharide
What is the systematic name of the cyclic monosaccharide shown here? Be sure to include the structural form as a component of the name. H OH CH₂OH H OH H H OH B-D-glucopyranoside B-D-glucopyranose B-D-glucofuranose Previous Page B-D-glucofuranoside OH -I H Next Page Page 10 of 25
Please don't provide handwritten solution .....
Can you draw the following. Around what's it suppose to look like. 1.) Clean Surface: [Gold surface of SPR]• SAM Formation: Gold surface - S - (CH2)11 - OH• Activation: Gold surface - S - (CH2)11 - CHO (using PCC)• Carbohydrate Coupling: Gold surface - S - (CH2)11 - CH=N - Carbohydrate (followed by NaBH3CN reduction) 2.) Clean Surface: [Gold surface of SPR]• SAM Formation: Gold surface - S - (CH2)11 - OH• Activation: Gold surface - S - (CH2)11 - CHO (using PCC)• Carbohydrate Coupling: Gold surface - S - (CH2)11 - CH=N - Carbohydrate (followed by NaBH3CN reduction)
Consider the structure shown below. он 3 5 CH; O CH, O H CH; O 1 H-N-CH,-C-N-CH;-C-N-CH-C-N-CH-C-N-CH-C-ơ 2 H. H H Fill in the blank with an integer (1, 2, 3, 4, 5..) as shown in the diagram or to represent a specified number. A hydrophilic side chain is indicated by the number
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