22. Convert the following Fisher projection into a Haworth projection. Draw only the alpha anomer (12 points)
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22. Convert the following Fisher projection into a Haworth
projection. Draw only the alpha anomer (12...
rt the following Fisher projection into a Haworth projection. Draw only the a anomer. (12 points)...
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
21. Are the following pairs of carbohydrates the same, completely different, constitutional isomers or stereoisomers? (12...
21.
Are the following pairs of carbohydrates the same, completely
different, constitutional isomers or stereoisomers? (12 points at 3
points each)
21. Are the following pairs of carbohydrates the same, completely different, constitutional isomers or reoisomers? (12 points at 3 points each) CHO CHO CHO H2OH a) он он он OH HO OH OH он b) H Ho Ho OH он он OH OH CH,OH CH,OH CH,OH OH HO CHO CHO 2OH OH он OH 011 HO OH Ho HO...
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
Question 2 (1 point) The Fisher projection below is equivalent to which Haworth structure if the...
Question 2 (1 point) The Fisher projection below is equivalent to which Haworth structure if the anomer formed is beta? CHO HO— 1 th 우 HI CH2OH CH OH OHA OH Он O2) CH2OH —о о ОН 3) CH,OH - О ОН ОН O4) CH OH ОН ОН ОН ОН
2. Convert each sugar below to its Haworth form. Draw the alpha anomer for a, the...
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
please draw the correct one if not in option and explain. HP Question 2 The Fisher projection below is equivalent t...
please draw the correct one if not in option and explain.
HP Question 2 The Fisher projection below is equivalent to which Haworth structure if the anomer formed is alpha? Cно H- OH но- -H н- Он H- -Он CH-он CH2OH 1) Он Он он Он CH2OH 2) OH Он OH
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
Convert the Fischer projection to the Haworth projection of the B-furanose form by moving the substituents...
Convert the Fischer projection to the Haworth projection of the
B-furanose form by moving the substituents to the appropriate
positions. The anomeric carbon is shown.
Convert the Fischer projection to the Haworth projection of the B-furanose form by moving the substituents to the appropriate positions. The anomeric carbon is shown. CH2OH =0 HO—C—H Cyclization H-¢-OH Answer Bank CH OH H—¢-OH CH,OH CH2OH
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): •...
3) a) Draw the Fischer projection of the following sugars and label them D or L....
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...
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
21.
Are the following pairs of carbohydrates the same, completely
different, constitutional isomers or stereoisomers? (12 points at 3
points each)
21. Are the following pairs of carbohydrates the same, completely different, constitutional isomers or reoisomers? (12 points at 3 points each) CHO CHO CHO H2OH a) он он он OH HO OH OH он b) H Ho Ho OH он он OH OH CH,OH CH,OH CH,OH OH HO CHO CHO 2OH OH он OH 011 HO OH Ho HO...
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
Question 2 (1 point) The Fisher projection below is equivalent to which Haworth structure if the anomer formed is beta? CHO HO— 1 th 우 HI CH2OH CH OH OHA OH Он O2) CH2OH —о о ОН 3) CH,OH - О ОН ОН O4) CH OH ОН ОН ОН ОН
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
please draw the correct one if not in option and explain.
HP Question 2 The Fisher projection below is equivalent to which Haworth structure if the anomer formed is alpha? Cно H- OH но- -H н- Он H- -Он CH-он CH2OH 1) Он Он он Он CH2OH 2) OH Он OH
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
Convert the Fischer projection to the Haworth projection of the
B-furanose form by moving the substituents to the appropriate
positions. The anomeric carbon is shown.
Convert the Fischer projection to the Haworth projection of the B-furanose form by moving the substituents to the appropriate positions. The anomeric carbon is shown. CH2OH =0 HO—C—H Cyclization H-¢-OH Answer Bank CH OH H—¢-OH CH,OH CH2OH
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): •...
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...
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