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2. Convert each sugar below to its Haworth form. Draw the alpha anomer for a, the...
Culhydrates 1. Complete th Complete the table by classifying each sugar sugar (A, B, C, D)...
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....
22. Convert the following Fisher projection into a Haworth projection. Draw only the alpha anomer (12...
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...
4. For each sugar below, characterize the anomer if a monosaccharide or the glycosidic bond(s) if...
4. For each sugar below, characterize the anomer if a monosaccharide or the glycosidic bond(s) if a di- or polysaccharide (e.g., B,B-2,3; if there is more than one glycosidic bond, draw an arrow from each label to its corresponding bond). CH,OH CH2OH CH OН но н H Н H Он Н OH н OH Он Н ОН O H Но он b. a. OH H OH CH-OH O H Но ОН Н CH2OH CH2 CH2OH он OCH CH3 Но н...
Given the Fischer projection of the sup sugar, draw its Haworth projection (B-anomer only) Fischer 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
Draw the following monosaccharide in the Beta anomer of the cyclic form 0 C= H- C-...
Draw the following monosaccharide in the Beta anomer of the cyclic
form
0 C= H- C- OH HO– –H н— — он H- C-OH Сн, он
Draw the Haworth projection structures for the B- anomer for these Fischer projections. raw Haworth projection...
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
ÇI-lagl- (2 pts) Use the Fischer projection shown below for the sugar D-altrose to draw a...
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
Draw the Haworth Projection for the compound represented by this model. also need help answering these...
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): •...
Carbohydrates 1. Label each of the monosaccharides shown below as a triose, tetrose, pentoso, or hexose....
Carbohydrates 1. Label each of the monosaccharides shown below as a triose, tetrose, pentoso, or hexose. но CH OH HT -он - он Н - ОН но -н но -Н но -н нон сньон он но -н НОН CH OH нон нон нон снон CH OH сон сон H- OH H- -он OH cң, он н-с-он Сн,он снон 2. Label each of the monosaccharides shown above as a ketose or aldose. 3. Identify all of the chiral carbons in the...
Spring 2020 E. Carbohydrates Part 1: In the box, draw the Fischer projection (linear conformation) that...
Spring 2020 E. Carbohydrates Part 1: In the box, draw the Fischer projection (linear conformation) that corresponds to the Haworth projection sugar given below. Note: This sugar is a ketose. (6 pts) СН2 она to 2 но - н 3 н он ч CH,OH Р +он 5 ОН 5 Н НО а H снаби о Сн,он ОН Н Part 2: Draw the Haworth projection of the given monosaccharide as a 6-sided a-pyranose ring. (7 pts) Н. 0 / са он...
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....
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...
4. For each sugar below, characterize the anomer if a monosaccharide or the glycosidic bond(s) if a di- or polysaccharide (e.g., B,B-2,3; if there is more than one glycosidic bond, draw an arrow from each label to its corresponding bond). CH,OH CH2OH CH OН но н H Н H Он Н OH н OH Он Н ОН O H Но он b. a. OH H OH CH-OH O H Но ОН Н CH2OH CH2 CH2OH он OCH CH3 Но н...
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
Draw the following monosaccharide in the Beta anomer of the cyclic
form
0 C= H- C- OH HO– –H н— — он H- C-OH Сн, он
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
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
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): •...
Carbohydrates 1. Label each of the monosaccharides shown below as a triose, tetrose, pentoso, or hexose. но CH OH HT -он - он Н - ОН но -н но -Н но -н нон сньон он но -н НОН CH OH нон нон нон снон CH OH сон сон H- OH H- -он OH cң, он н-с-он Сн,он снон 2. Label each of the monosaccharides shown above as a ketose or aldose. 3. Identify all of the chiral carbons in the...
Spring 2020 E. Carbohydrates Part 1: In the box, draw the Fischer projection (linear conformation) that corresponds to the Haworth projection sugar given below. Note: This sugar is a ketose. (6 pts) СН2 она to 2 но - н 3 н он ч CH,OH Р +он 5 ОН 5 Н НО а H снаби о Сн,он ОН Н Part 2: Draw the Haworth projection of the given monosaccharide as a 6-sided a-pyranose ring. (7 pts) Н. 0 / са он...
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