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Draw the Haworth projection structures for the B- anomer for these Fischer projections. raw Haworth projection...
Given the Fischer projection of the sup sugar, draw its Haworth projection (B-anomer only) Fischer Projection H Haworth Projection (B-anomer) CH, OH on CH OH 5. Identify the glycosidic linkages for the following disaccharides. Determine whether the disaccharides are reducing or non-reducing sugars. сон OH OH OH OH CHOH Снон не Он н Снон онон | CH, OH нон CH-OH
3) a) Draw the Fischer projection of the following sugars and label them D or L. HO b) Draw the most stable chair conformation of the b-anomer of the hemiacetal of the following aldohexose: 3) a) Draw the Fischer projection of the following sugars and label them Dor L. НО. H CHO он НО H он Н. ОН НО. CHO ли нон н он b) Draw the most stable chair conformation of the B-anomer of the hemiacetal of the following...
22. Convert the following Fisher projection into a Haworth projection. Draw only the alpha anomer (12 points) 21. Are the following pairs of carbohydrates the same, completely different, constitutional isomers or stereoisomers? (12 points at 3 points each) CHO CHO CHO сњон он OH он он CH2OH он он он он он но он но но он он CH2OH CH2OH он CHO CHO CHO сњон он он он он он но он но но Ho но он но он OH...
rt the following Fisher projection into a Haworth projection. Draw only the a anomer. (12 points) CHO но -н нон но o -н bordando o HH -OH CH,OH он contrario si wololo zelo (tiga) audio to 10 mon si batu
3. Convert the following Fischer projection to Haworth projections си, •Н о НО. -Н по Н H -ой сной 4. Identify the glycosidic linkage in the following compounds. che 1 chte ok ol и и ol и но и on h on che oll CH2OH 얻 on Н 애 к до н. и ои
1. Turn the following Fischer projections into line structures. H. CEO dawn vн-Ф-сі НА-ОН HOAH CH2OH CH2OH c=o н +ОН НО-НН HO -Н CH2OH HOC=0 нон нон НЕОН НЕОН CH2OH
12.36 Draw Fischer projections for each of the following dash-wedge structures: a. CHO b. CHO C. CHO с но : Br CH OH Ho : н СН,ОН н : ОН СН,ОН
Draw the Haworth Projection for the compound represented by this model. also need help answering these questions that go along with the model i included Model 5 (This model does not rotate) Н H CH,OH С C НО НО C Н C с. H ОН) ОН Н (b) Haworth projection formulas of cyclic monosaccharides. View model #5 of the cyclic monosaccharide and answer the following: • Is the ring structure a pyranose (6 sides) or a furanose (5 sides): •...
Culhydrates 1. Complete th Complete the table by classifying each sugar sugar (A, B, C, D) below based on carbonyl group and number of carbons (c.8. aldohexose, ketotriose, etc.). Classify them as an antiomer. Indicate the number of chiral carbons for each sugar. Sugar Classification based on carbonyl group and number of carbons Lor D enantiomer Number of chiral carbons н-с-он HO-6-H. н-с-он ін,он CH,OH C=0 HO-C-H н-с-он HO-C-H. ён,он снон c=0 | HO-C-H ін,он H-C-OH CH, OH CD 2....
35. Enzymatic processing to break down glycogen into glucose occurs at: a. a reducing end. b. a non-reducing end. c. reducing and non-reducing ends simultaneously. d. branch points exclusively. 36. Which furanose is the B anomer of the monosaccharide given by the Fischer projection below? CH2OH 0= но о он a OH но о K он но, HOT о, -н он о. он Он KOH /он но TOH Нон но LOH HO но н но - он но -ОН -н...