Question 2 (4 points) In the following Haworth structure, is this the A or B anomer?...
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
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....
Draw the Haworth projection structures for the B- anomer for these Fischer projections. raw Haworth projection structures for the B-anomer for these Fisch ojections CHO CHO ОН НО -Н H Н -ОН НО -Н Н -ОН CH2OH (D)-idose НО-НН НО-НН ньон снон (D)-galactose
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
2. Convert each sugar below to its Haworth form. Draw the alpha anomer for a, the beta for b. CH OH c=0 но-с-н HO-c-H H-C-OH a. CH OH u-u-u-u-u- III н-с-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): •...
Chem 1205 Recitation #10 Questions 3: Use the templates provided to draw the Haworth Projections for a- & B-anomers: HOH но -н но -н H- OH CH, OH HH tilt 'tip' structure over Rotate bottom carbon to put -OH at end Draw Haworth canomer B-anomer Question 4:Label the glycosidic linkages in the given disaccharides: сон - AM OHH CH 6-18 IVO
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...
7. For the following monosaccharides, give the corresponding Fischer projection. CH OH —0 ОН CH,он Но —0 ОН НО У (он но У HO сно F 8. For the following monosaccharides, give one possible Haworth structure. CHO H- OH HOH Нонн — он нон CH OH CH OH от т т н-
ÇI-lagl- (2 pts) Use the Fischer projection shown below for the sugar D-altrose to draw a Haworth projection of the beta- 2. pyranose form of this sugar. но -Н H- OH H- OH OH H- CH-ОН 1