Draw the Haworth projection of both pyranose and both furanose forms of D-Idose with all stereocenters accurately portrayed. You do not have to label thename of the form you drewH-COHO-HH-OHHO-HOH OHHOH2CH-OHCHOOH OHCH2OHD-Idose line drawingD-Idose Fischer projection

I can help you with that. The Fischer projection of D-Idose is given in the question. We can use…

Answered: Draw the Haworth projection of both…

Organic And Biological Chemistry

7th Edition

ISBN:9781305081079

Author:STOKER, H. Stephen (howard Stephen)

Publisher:STOKER, H. Stephen (howard Stephen)

Chapter7: Carbohydrates

Section: Chapter Questions

Problem 7.80EP

See similar textbooks

Similar questions

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
1. Draw Haworth projections of B-D-arabinofuranose and a-L-mannopyranose. 2. Consider the structure of the disaccharide drawn at right: НО `CH2 В ОН (a) Give the names and D/L designation for the two monosaccharides linked together. H,C-O OHO „OH OH А: НО НО A В: ОН (b) In the structure, circle the anomeric carbon of each saccharide. (c) Is each saccharide present in its a or ß anomer? Specify both A and B (d) Would this disaccharide undergo mutarotation? Why or why not? (e) Would this disaccharide react with Tollens and/or Benedicts reagent? Why or why not? (f) There are two reasons this is very unlikely to be a naturally occurring disaccharide. What about its structure suggests this is true? Give both reasons.
Glucose is the most abundant monosaccharide. From memory, draw glucose in(a) the Fischer projection of the open chain.(b) the most stable chair conformation of the most stable pyranose anomer.(c) the Haworth projection of the most stable pyranose anomer
2) a-Draw the proper flat, Haworth form and most stable chair conformation for the B- anomer of L- glucopyranose b- Write the systematic name of this compound O: HO- НО—н НО H FOH HO-H -O- L-Gulose
Allose is the C3 epimer of glucose. Draw the cyclic hemiacetal form of d-allose, first inthe chair conformation and then in the Haworth projection
The Fischer projection for D-idose is shown. Provide the Haworth projection and chair conformations, for the a-anomer. CHO HO H HO H H OH H OH CH₂OH
The monosaacharide talose is shown as a Fischer projection. Which is a correct Haworth projection for talose СНО HO HO H HO H H- -ОН CH,OH CHOH HO OH HO. OH O OH
Draw Fischer projections for the product(s) formed by reaction of d-ribose with the following. In addition, state whether each product is optically active or inactive Q. HNO3, warm
Draw the cyclic hemiacetal forms of d-mannose and d-galactose both as chair conformations and as Haworth projections. Mannose is the C2 epimer of glucose, and galactoseis the C4 epimer of glucose.

Recommended textbooks for you

Organic And Biological Chemistry

Chemistry

ISBN:

9781305081079

Author:

STOKER, H. Stephen (howard Stephen)

Publisher:

Cengage Learning,

General, Organic, and Biological Chemistry

Chemistry

ISBN:

9781285853918

Author:

H. Stephen Stoker

Publisher:

Cengage Learning

Introduction to General, Organic and Biochemistry

Chemistry

ISBN:

9781285869759

Author:

Frederick A. Bettelheim, William H. Brown, Mary K. Campbell, Shawn O. Farrell, Omar Torres

Publisher:

Cengage Learning

Organic And Biological Chemistry

Chemistry

ISBN:

9781305081079

Author:

STOKER, H. Stephen (howard Stephen)

Publisher:

Cengage Learning,

General, Organic, and Biological Chemistry

Chemistry

ISBN:

9781285853918

Author:

H. Stephen Stoker

Publisher:

Cengage Learning

Introduction to General, Organic and Biochemistry

Chemistry

ISBN:

9781285869759

Author:

Frederick A. Bettelheim, William H. Brown, Mary K. Campbell, Shawn O. Farrell, Omar Torres

Publisher:

Cengage Learning

Organic Chemistry

Chemistry

ISBN:

9781305080485

Author:

John E. McMurry

Publisher:

Cengage Learning

Organic Chemistry

Chemistry

ISBN:

9781305580350

Author:

William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Publisher:

Cengage Learning

Chemistry for Today: General, Organic, and Bioche…

Chemistry

ISBN:

9781305960060

Author:

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

Publisher:

Cengage Learning

SEE MORE TEXTBOOKS

Draw the Haworth projection of both pyranose and both furanose forms of D- Idose with all stereocenters accurately portrayed. You do not have to label the name of the form you drew H-CO HO -H H -OH HO -H OH OH HOH2C H- OH CHO OH OH CH2OH D-Idose line drawing D-Idose Fischer projection