Why does CO2H have priority over CH2CO2H? (This molecule is in fischer projection and is an S molecule)
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Why does CO2H have priority over CH2CO2H? (This molecule is in
fischer projection and is an...
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
OH Draw a Fischer projection for the following compound, placing the -CO2H up at the top. Rotation between Cry and...
OH Draw a Fischer projection for the following compound, placing the -CO2H up at the top. Rotation between Cry and C, might be needed но a. Assign R/S configuration to the chiral centers, b. Draw its enantiomer, and C. Draw a diastereomer. (2) OH HOC
A Fischer projection of a monosaccharide is shown below: A Fischer projection of a monosaccharide is...
A Fischer projection of a monosaccharide is shown
below:
A Fischer projection of a monosaccharide is shown below: CHO H + -OH CH2OH Classify this monosaccharide (e.g., aldotriose) Does it have the D or L configuration? A Fischer projection of a monosaccharide is shown below: CH2OH Ç=0 H- -OH HO -H CH OH Classify this monosaccharide (e.g., aldotriose) Does it have the D or L configuration?
Question 57 Choose the Fischer projection for the open-chain form of the following cyclic monosaccharide. ОН...
Question 57 Choose the Fischer projection for the open-chain form of the following cyclic monosaccharide. ОН НО- ОН НО ОН о H н ОН HO н НО Н НО H OH О Н H ОН но H НО H Н ОН OH о H Н ОН
Question 57 Choose the Fischer projection for the open-chain form of the following cyclic monosaccharide. ОН...
Question 57 Choose the Fischer projection for the open-chain form of the following cyclic monosaccharide. ОН НО- ОН НО ОН о H н ОН HO н НО Н НО H OH О Н H ОН но H НО H Н ОН OH о H Н ОН
Select all of the descriptions that are accurate for this molecule of glucose CH2OH н с—...
Select all of the descriptions that are accurate for this molecule of glucose CH2OH н с— о, н VH С он н C OH но с H Он it is a hexose it is in the alpha form it is in the beta form it is a furanse it is a pyranose it is a Haworth projection It is a Fischer projection Select all of the descriptions that are accurate for this molecule. CH-он Он Он ОН It is a...
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...
4. Consider the following Fischer Projection: CH, OH I 9 CH OH A Does this represent...
4. Consider the following Fischer Projection: CH, OH I 9 CH OH A Does this represent a monosaccharide, a disaccharide, a trisaccharide or something else? B Are any chiral carbons present? If so, circle each one. C Does this represent an aldose or a ketose? Explain your response and draw a box around the relevant functional group. D Give the molecular formula for this compound. E Is this compound classified as an L-isomer or a D- isomer? your response. Explain...
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
rever; mbine - you 13.78 Identify the Fischer projection A to D that matches each of...
rever; mbine - you 13.78 Identify the Fischer projection A to D that matches each of the following: (13.1, 13.3) a. the L enantiomer of mannose b. a ketopentose c. an aldopentose d. a ketohexose о но СН,ОН НЕОН CHOH С=0 НЕОН H- С=0 НЕ ОН НО -н НО-н Но Hн НО -Н НЕОН НО - H н -ОН НОН CHOH СН,ОН СН,ОН CH,OH -ОН dic D
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
OH Draw a Fischer projection for the following compound, placing the -CO2H up at the top. Rotation between Cry and C, might be needed но a. Assign R/S configuration to the chiral centers, b. Draw its enantiomer, and C. Draw a diastereomer. (2) OH HOC
A Fischer projection of a monosaccharide is shown
below:
A Fischer projection of a monosaccharide is shown below: CHO H + -OH CH2OH Classify this monosaccharide (e.g., aldotriose) Does it have the D or L configuration? A Fischer projection of a monosaccharide is shown below: CH2OH Ç=0 H- -OH HO -H CH OH Classify this monosaccharide (e.g., aldotriose) Does it have the D or L configuration?
Question 57 Choose the Fischer projection for the open-chain form of the following cyclic monosaccharide. ОН НО- ОН НО ОН о H н ОН HO н НО Н НО H OH О Н H ОН но H НО H Н ОН OH о H Н ОН
Question 57 Choose the Fischer projection for the open-chain form of the following cyclic monosaccharide. ОН НО- ОН НО ОН о H н ОН HO н НО Н НО H OH О Н H ОН но H НО H Н ОН OH о H Н ОН
Select all of the descriptions that are accurate for this molecule of glucose CH2OH н с— о, н VH С он н C OH но с H Он it is a hexose it is in the alpha form it is in the beta form it is a furanse it is a pyranose it is a Haworth projection It is a Fischer projection Select all of the descriptions that are accurate for this molecule. CH-он Он Он ОН It is a...
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...
4. Consider the following Fischer Projection: CH, OH I 9 CH OH A Does this represent a monosaccharide, a disaccharide, a trisaccharide or something else? B Are any chiral carbons present? If so, circle each one. C Does this represent an aldose or a ketose? Explain your response and draw a box around the relevant functional group. D Give the molecular formula for this compound. E Is this compound classified as an L-isomer or a D- isomer? your response. Explain...
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
rever; mbine - you 13.78 Identify the Fischer projection A to D that matches each of the following: (13.1, 13.3) a. the L enantiomer of mannose b. a ketopentose c. an aldopentose d. a ketohexose о но СН,ОН НЕОН CHOH С=0 НЕОН H- С=0 НЕ ОН НО -н НО-н Но Hн НО -Н НЕОН НО - H н -ОН НОН CHOH СН,ОН СН,ОН CH,OH -ОН dic D
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