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 the product formed when each monosaccharide is oxidized with Benedict’s reagent.
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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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Modify the structure of kojiblose to show the monosaccharide products that form from hydrolysis. draw the structures in any arrangement, so long as they aren't touching
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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