For the following monosaccharide, draw the products formed when treated with each reagent.HH-OHHOHHOHH―-OHCH₂OHPart 1 of 2H2 in the presence of a Pd catalyst.Modify the Fischer projection of the monosaccharide to represent the product.HH-ОНHOHHOHH-OHCH₂OHPart 2 of 2Benedict's reagent.Modify the Fischer projection of the monosaccharide to represent the product.HH-OHHO-НHOHH-OHCH₂OH☐:G☐E☐: ☑PG

Step 1:When an aldehyde is reacted with hydrogen gas (H₂) in the presence of a palladium catalyst…

Answered: For the following monosaccharide, draw…

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

Given Tagatose, Briefly explain its expected reaction (based on their structural formula) to the different qualitative tests for carbohydrates which are: (a)Barfoed’s test (b)Seliwanoff’s test (c) Iodine’s test
Please draw the major product(s) of the following reaction and show the mechanism. Is there a reason why one stereochemistry is preferred over the other for this reaction?
Which of the following is the cyclic form of an L saccharide? 1) II) CH2OH OH H CH2OH H H H ОН OH H ОН ОН OH H ОН II) IV) H OH ОН CH2OH CH2OH CH2OH H H. H ОН H H H OH ОН ОН OH
Give the systematic name of the the disaccharide shown below: CH2OH CH2OH H H Н ОН Н Н ОН Н H H ОН H. ОН H ОН
Given Tagatose, Briefly explain its expected reaction (based on their structural formula) to the different qualitative tests for carbohydrates which are: (a) Molisch’s test (b)Fehling’s test (c) Bial’s test
Describe how the functional units for beta carotene, xanthophyll, chlorophyll A, and chlorophyll B are different. Be sure to identify the subunits that adhere to paper during chromatography.
From the following monosaccharides, identify the a anomers. Select all that apply. Select one or more: OH он OH OH O a. OH OH HO но- Ob. ÓH H OH HO но- он H OH O c. HO OH ÓH ÓH d.
Considering the monosaccharide transformation given below, what is the name of the depicted reaction? но. OH OH OPN v OH OH Amination Anomeric dehydration Reduction C1 oxidation C6 oxidation
When D-gulose forms a ring structure, a) b) a ketone and a hydroxyl group react to form a hemiketal. the ring is unstable at neutral pH. the ring contains four stereogenic centers. an intramolecular reaction creates a glycosidic bond.
Will the synthesis of 9,10-dihydroanthracene-9,10-α,β-succinic anhydride via Diels-Alder reaction occur faster under photochemical conditions? Explain.
A decapeptide has the following acid composition; Al2,Arg,Cys,Glu,Leu,Phe,Val Partial hydrolysis yield the following tripeptides; Cys-Glu-Leu+Gly-Arg-Cys+Leu-Ala-Ala+Lys-Val-Phe-Gly Reaction of the decapeptide with 2,4-dinitrofluorobenzene yields 2,4-dinitrophenylysine. From the experimental data, deduce the primary structure of the decapeptide. Suggest a scheme you will follow to synthesize the dipeptide Ala-Gly.
Draw structural formulas for the alkoxide ion and the alkyl(aryl)bromide that may be used in a Williamson synthesis of the ether shown. CH3CH2CH2CH2-0-CH2CH2CH2CH3 • You do not have to consider stereochemistry. • Do not include counter-ions, e.g., Na*, I, in your answer. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. O Separate structures with + signs from the drop-down menu.

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