Homework Answers
Add Answer to:
Classify each monosaccharide by the type of carbonyl group and the number of carbons in the...
1. For each of the following sugars: state the classification (by number of carbons and carbonyl type, like aldotetr...
1. For each of the following sugars: state the classification (by number of carbons and carbonyl type, like aldotetrose), whether the sugar is D- or L-form, and draw the enantiomer. но СН,ОН н-с- OH но-с-н н-с- он нс- он CH OH с=0 но -н нон но -н СН,ОН CH2OH 1 С=0 но но НО -н -н -н CHOH н-с- он CH OH
Classify each of the following monosaccharides by the type of carbonyl group and the number of...
Classify each of the following monosaccharides by the type of
carbonyl group and the number of carbons (for example, a
monosaccharide with an aldehyde and three carbons is an
aldotriose).
ketotriose aldohexose CH2OH CH2OH aldotetrose 이 H CH OH ketotetrose I 운 우 ketopentose HH H1 ketohexose CHOH CH2OH aldopentose aldotriose
Question 2 of 33 > Classify the monosaccharides according to the position of the carbonyl group...
Question 2 of 33 > Classify the monosaccharides according to the position of the carbonyl group and the number of carbon atoms in the molecule. Сн,он CHO —н но O OH ону H- -он OH CH OH OH O aldopentose ketotriose ketotetrose ketohexose ketopentose ketotetrose aldohexose aldopentose aldotetrose O O ketopentose O aldotetrose aldotriose O CH2OH OH 0 < HO CH OH OH O aldotetrose O aldohexose O ketohexose O aldopentose O ketopentose Oketotetrose
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...
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....
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...
1) SHOW WORK STEP By STEP below is Figure 7-3 Recognizing Epimers Using Figure 7-3, identify the epimers of (a) D-...
1) SHOW WORK STEP By STEP
below is Figure 7-3
Recognizing Epimers Using Figure 7-3, identify the epimers of (a) D-allose, (b) D-gulose, and (c) D-ribose at C-2, C-3, and C-4. Answer Epimers differ by the configuration about only one carbon. (a) D-altrose (C-2), D-glucose (C-3), D-gulose (C-4) (b) D-idose (C-2), D-galactose (C-3), D-allose (C-4) (c) D-arabinose (C-2), D-xylose (C-3) (a) D-Aldoses Three carbons Four carbons Five carbons но не HO -OH н-с-он CH, OH D-Glyceraldehyde но-с-н H-C-OH снион D-Threose...
C=O 2. Which of the following is an example of an aldopentose? Circle your answer. СН,ОН...
C=O 2. Which of the following is an example of an aldopentose? Circle your answer. СН,ОН CH,он CH н-с-он H-6-H H-C-OH HO-C-H. H-C-H H-C-OH H-C-OH H-6-H H-C-OH CH,OH CH,OH CH OH 3. In the L- isomer of a Fischer projection of a monosaccharide, the -OH group furthest from the carbonyl is written. Circle your answer. on the left of the top chiral carbon. on the left of the middle chiral carbon. on the left of the bottom chiral carbon. on...
13.34 For each of the following give the monosaccharide units produced by hydrolysis, the type of...
13.34 For each of the following give the monosaccharide units produced by hydrolysis, the type of glycosidic bond, and the name of the disaccharide including a or B: а. СН,ОН СН,ОН НА - 0 H н Он н/ о он н НО Н н ОН НОН СН,ОН - 0 Н НИ / Н ОН Н HO н Оно НОСНО ННО Н СН,ОН OHн
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
1. For each of the following sugars: state the classification (by number of carbons and carbonyl type, like aldotetrose), whether the sugar is D- or L-form, and draw the enantiomer. но СН,ОН н-с- OH но-с-н н-с- он нс- он CH OH с=0 но -н нон но -н СН,ОН CH2OH 1 С=0 но но НО -н -н -н CHOH н-с- он CH OH
Classify each of the following monosaccharides by the type of
carbonyl group and the number of carbons (for example, a
monosaccharide with an aldehyde and three carbons is an
aldotriose).
ketotriose aldohexose CH2OH CH2OH aldotetrose 이 H CH OH ketotetrose I 운 우 ketopentose HH H1 ketohexose CHOH CH2OH aldopentose aldotriose
Question 2 of 33 > Classify the monosaccharides according to the position of the carbonyl group and the number of carbon atoms in the molecule. Сн,он CHO —н но O OH ону H- -он OH CH OH OH O aldopentose ketotriose ketotetrose ketohexose ketopentose ketotetrose aldohexose aldopentose aldotetrose O O ketopentose O aldotetrose aldotriose O CH2OH OH 0 < HO CH OH OH O aldotetrose O aldohexose O ketohexose O aldopentose O ketopentose Oketotetrose
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...
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....
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...
1) SHOW WORK STEP By STEP
below is Figure 7-3
Recognizing Epimers Using Figure 7-3, identify the epimers of (a) D-allose, (b) D-gulose, and (c) D-ribose at C-2, C-3, and C-4. Answer Epimers differ by the configuration about only one carbon. (a) D-altrose (C-2), D-glucose (C-3), D-gulose (C-4) (b) D-idose (C-2), D-galactose (C-3), D-allose (C-4) (c) D-arabinose (C-2), D-xylose (C-3) (a) D-Aldoses Three carbons Four carbons Five carbons но не HO -OH н-с-он CH, OH D-Glyceraldehyde но-с-н H-C-OH снион D-Threose...
C=O 2. Which of the following is an example of an aldopentose? Circle your answer. СН,ОН CH,он CH н-с-он H-6-H H-C-OH HO-C-H. H-C-H H-C-OH H-C-OH H-6-H H-C-OH CH,OH CH,OH CH OH 3. In the L- isomer of a Fischer projection of a monosaccharide, the -OH group furthest from the carbonyl is written. Circle your answer. on the left of the top chiral carbon. on the left of the middle chiral carbon. on the left of the bottom chiral carbon. on...
13.34 For each of the following give the monosaccharide units produced by hydrolysis, the type of glycosidic bond, and the name of the disaccharide including a or B: а. СН,ОН СН,ОН НА - 0 H н Он н/ о он н НО Н н ОН НОН СН,ОН - 0 Н НИ / Н ОН Н HO н Оно НОСНО ННО Н СН,ОН OHн
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
Most questions answered within 3 hours.
-
Hook Industries is considering the replacement of one of its old
metal stamping machines. Three alternative...
asked 13 seconds from now -
Polaski Company manufactures and sells a single product called a
Ret. Operating at capacity, the company...
asked 31 seconds ago -
The Bureau of Alcohol, Tobacco, and Firearms (BATF) has been
concerned about lead levels in California...
asked 3 minutes ago -
I just did a lab on determination of an equilibrium constant
through the reaction EtAc (aq)...
asked 17 minutes ago -
The potential in a region of space due to a charge distribution
is given by the...
asked 9 minutes ago -
Assume that there is unburned pentane (C5H12 ) in automobile
exhaust. Write an expression for the...
asked 12 minutes ago -
A capacitor is formed from two concentric spherical conducting
shells separated by vacuum. The inner sphere...
asked 18 minutes ago -
Eight White adults had been convicted of crimes of hate for
their anti-Asian behaviors and were...
asked 19 minutes ago -
FInd the answer to each by first reducing the fractions as much
as possible
1. P...
asked 24 minutes ago -
replaced John Lewis as the chairman of the Student Non-Violent
Coordinating Committee (SNCC)?
asked 42 minutes ago -
Determine the conjugate base for each of the following
acids:
HSO4-
CH3CH2COOH
Identify all of the...
asked 36 minutes ago -
How many mole of potassium hydroxide are in 27.5 mL of
0.250 M potassium hydroxide soltion?...
asked 44 minutes ago