Please correct answer and don't use hand rating Convert the aldohexose to the a anomer using a Haworth projection.H.C:HO-HHOHHO.HH·- ОНCH₂OH

Step 1:We are given a fisher projection of a aldohexos .We need to convert this into cyclic form,…

Answered: Convert the aldohexose to the a anomer…

Chemistry for Today: General, Organic, and Biochemistry

9th Edition

ISBN:9781305960060

Author:Spencer L. Seager, Michael R. Slabaugh, Maren S. Hansen

Publisher:Spencer L. Seager, Michael R. Slabaugh, Maren S. Hansen

Chapter17: Carbohydrates

Section: Chapter Questions

Problem 17.23E

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Similar questions

Draw Haworth projection formulas for the a-anomer of monosaccharides with each of the following Fischer projection formulas. a. CHO HOH H- HO- H -ОН -Η OH CH₂OH b. CHO H -OH H -ОН HO H CH₂OH
Draw the product formed when each monosaccharide is oxidized with Benedict’s reagent.
Which structures represent ketose, aldose, and alditol?
classify the following monosaccharides as aldoses/ketoses, triose/tetrose/pentose/hexose/ L/D enantiomer, and a-/Banomer when applicable.
7. Draw the Haworth structure for the following monosaccharides a. H НО H c=0 H + но - н 3 4 Н 5 - ОН - OH 애 CH₂OH 6 D-Mannose b. H 0 = с H - C - OH HO-C - H H - C - OH H - C - ОН CH₂OH Glucose
m) Which pyranose ring (A, B, C, or D) in the tetrasaccharide below is derived from D-altrose? The Fischer projections for the four aldohexoses that make up this tetrasaccharide are shown below. B C D HOH CHO CHO CHO CHO HO+H HTOH Fонно н HOH HOH H-OH H-OH H-+-OH H-TOHHOH HOH H+OH HOHнтон нон CHOH CHOH CHOH CHOH De D-glue Dalose Datrone i NH Į HOH STEP 1 OH, HO- answer 1. Just add arrows and charges for steps 1, 2, and 3 in formation of this enamine з no arrows needed here OH н Н ЮН -OH STEP 3 :ÖH н H STEP 2 на это про за поч
Which one is b-D glucose and which one is a-L glucose ? 2. Which one is b-fructose and which a-L fructose?
1. In the space provided, draw a Haworth projection for the alpha anomer of the following monosaccharide Fischer projection. H но CHO OH -H H- OH H- FOH CH₂OH
14․ Identify the following as an ? or ? form and draw the Haworth structure of the other anomer. 15․ Below are the Fischer projections of monosaccharides.
H Convert the aldohexose to the a anomer using a Haworth projection. C=0 HO -H HO H H .OH H OH CH₂OH G 모
1
N-NHPH CHO CH2OH H- C=N-NHPH Но- -H- 3 equiv Но- -H- 3 equiv Но- PHNHNH2 PHNHNH, H- H- OH H- -O- H- H- -HO- H- -HO- ČH2OH ČH2OH ČH2OH D-glucose osazone D-fructose + NH3 + PHNH2 + 2 H20 The final step in the formation of the osazone from glucose is the reaction of the keto imine with 2 equivalents of phenylhydrazine to yield the osazone plus ammonia. This reaction involves the following intermediate steps: 1. Addition of phenylhydrazine to the imine and proton transfer to yield intermediate 1; 2. Elimination of ammonia to yield phenylhydrazone 2; 3. Addition of phenylhydrazine to the ketone to yield tetrahedral intermediate 3; 4. Proton transfer yields carbinolamine 4; 5. Elimination of water yields the final product osazone. Write out the mechanism on a separate sh of paper and then draw the structure of tetrahedral intermediate 3. NH НО- -H H- -ОН H- -ОН ОН Glucose keto imine Previous Ne

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Convert the aldohexose to the a anomer using a Haworth projection. H. C: HO- H H OH HO. H H· - ОН CH₂OH