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This question has mulüple parts. We all ule pulu tu get the most points. a Choose...
30. Which of the choices below is the enantiomer of D-glucose? сно сно нон HO-EH сно...
30. Which of the choices below is the enantiomer of D-glucose? сно сно нон HO-EH сно на-он D-glucose Іно-Ен н -он но-Ен EH,OH сно но н-он но -н нон Сн,он но-Ен на-он но -н но-Ен н -он нон CHO но -н н-он но-Ен нон снен CHOH Сн,он 3. Which of the following structures is an a-anomer? Сн,он —о, он o ноноон нонс осн он — о оно сн, он он онон он он он он тон КСн,он y CH, OH...
Select the highest energy form of adenosine from the following images. View Available Hint(s) CH2----P---o OES...
Select the highest energy form of adenosine from the following images. View Available Hint(s) CH2----P---o OES - - - NH2 och-O-P-O-P-O 6- OH OH Nhe N O CH2-O-P-0 A по но-р-р-р-р-р-о Кино-о-о- OH OH CH2-O-P OH OH CH-0-Р-о" Кни ОН ОН осн. Кн н он он o o o сне-o-p-o-p-o-p-o" Hно-о-о- он он
Question 1 (1 point) Choose the reducing sugars (select all that apply): СН,ОН СН,ОН не —...
Question 1 (1 point) Choose the reducing sugars (select all that apply): СН,ОН СН,ОН не — о он н ОН НА // Н v H ОН НА у н н н ОН н ОН CH,OH 1 ОНОН а снион и онон н СН,ОН ОН —0, ОН ОН ОН CH2OH -о- слъ We were unable to transcribe this imageQuestion 2 (1 point) Monosaccharide B can be cat Сн,ОН н Дон ү0 р. Н ОН HOCH2 ОН HV СН,ОН В. Г ОН...
Use the figure below to answer the following question about glycolysis. Where did the phosphate group...
Use the figure below to answer the following question about glycolysis. Where did the phosphate group come from to create the second molecule shown? GLYCOLYSIS: Energy Investment Phase ATP Glucose сн,он Glucose 6-phosphate CH,OẠP Fructose 6-phosphate CH,O 2 CH2OH ADP он Кон WAO HO он HOOH OH Hexokinase VOH OH HO KOH Phosphogluco- isomerase но н ADP ATP Glycolysis Glucose Hexokinase
Ch 16.1 Give the major product(s) or the following reaction ao,a OH N ? OH io...
Ch 16.1
Give the major product(s) or the following reaction ao,a OH N ? OH io OH H There is no reaction under these conditions or the correct product is not listed here Gve the major product(s) of the following reaction COCH OH N H OH 0 OH H There is no reaction under these conditions or the correct product is not listed here. В 1) BAIH (-Bu), (-78°C) (0.5 moles) 2) ное ? оо н ОН ОН OCH, OH...
Please show all work. Will rate high! Use the Henderson–Hasselbalch (H-H) equation to answer the following...
Please show all work. Will rate high!
Use the Henderson–Hasselbalch (H-H) equation to answer
the following question:
Calculate the concentration of the glutamine anion when 0.50 M of glutamine is at a physiological pH of 7.4. The pka of the a-amine group is 9.13. (Answer in mm) Match the name with the structure for each of the D-aldoses. CHO CHO но CHO H он H Но H H ОН H он HOH H он CHO но -Н H ОН но...
4.23,4.24 & 4.26 thank you 156 CHAPTER 4 Introduction to Organic Compounds Practice Problems 4.21 4.23...
4.23,4.24 & 4.26 thank you
156 CHAPTER 4 Introduction to Organic Compounds Practice Problems 4.21 4.23 Draw the condensed structural formula for each of the following alkyl groups: a. propyl b. methyl 4.24 Give the correct name for each of the following substituents: a. CH CH - b. CH3CH,CHCH- c. I- 4.25 Draw the skeletal structure for each of the following compounds: a. 2,3-dimethylpentane b. 2-ethyl-1,4-dimethylcyclohexane c. 1,2-dichlorohexane 4.26 Draw the skeletal structure for each of the following compounds: a....
This question has multiple parts. Work all the parts to get the most points. Galactose has...
This question has multiple parts. Work all the parts to get the most points. Galactose has the following structure: н он HO H Но. CHO нН но Н H OH a How many chirality centers are present in this molecule? Chirality centers: 4 How many total stereoisomers does Galactose have? Stereoisomers: 16 Correct b Draw the structure of the enantiomer of Galactose. Use the wedge hash bond tools to indicate stereochemistry where it exists Oo0
1. You have given all the enzymes and intermediates in glycolysis. Choose the right enzymes and...
1. You have given all the enzymes and intermediates in glycolysis. Choose the right enzymes and intermediates and draw the glycolytic pathway. Decorate the diagram by adding ATP, ADP, H", NADH, NAD', P, and H20 where necessary. All the steps are reversible except 1, 3 and 10; draw appropriate arrow. First arrange the reactants in the correct order. Reactants/intermediates: 3-phosphoglycerate glucose Phosphoenolpyruvate dihydroxyacetone phosphate Pyruvate glucose 6-phosphate 1,3-bisphosphoglycerate fructose 6-phosophate 2-phosphoglycerate glyceraldehyde 3-phosphate fructose 1,6-bisphosphate Enzymes: Phosphoglucoisomerase phosphoglycerate kinase phosphoglycerate...
18. Which of the following compound(s) would undergo mutarotation in aqueous solution? 19. Draw the chair...
18.
Which of the following compound(s) would undergo mutarotation in
aqueous solution?
19. Draw the chair conformation of a-D-galactopyranose.
20. Which of the following compound(s) is a glycoside?
21. Provide the reagents neccesary to carry out the following
conversion.
22. Predict the product(s) for the following reaction.
23. D-glucose & D-galactose are ______epimers of each
other.
24. Predict the product(s) for the following reaction.
25. Which of the following compound(s) would produce D-glucose
and D-mannose when treated with HCN followed...
30. Which of the choices below is the enantiomer of D-glucose? сно сно нон HO-EH сно на-он D-glucose Іно-Ен н -он но-Ен EH,OH сно но н-он но -н нон Сн,он но-Ен на-он но -н но-Ен н -он нон CHO но -н н-он но-Ен нон снен CHOH Сн,он 3. Which of the following structures is an a-anomer? Сн,он —о, он o ноноон нонс осн он — о оно сн, он он онон он он он он тон КСн,он y CH, OH...
Select the highest energy form of adenosine from the following images. View Available Hint(s) CH2----P---o OES - - - NH2 och-O-P-O-P-O 6- OH OH Nhe N O CH2-O-P-0 A по но-р-р-р-р-р-о Кино-о-о- OH OH CH2-O-P OH OH CH-0-Р-о" Кни ОН ОН осн. Кн н он он o o o сне-o-p-o-p-o-p-o" Hно-о-о- он он
Question 1 (1 point) Choose the reducing sugars (select all that apply): СН,ОН СН,ОН не — о он н ОН НА // Н v H ОН НА у н н н ОН н ОН CH,OH 1 ОНОН а снион и онон н СН,ОН ОН —0, ОН ОН ОН CH2OH -о- слъ We were unable to transcribe this imageQuestion 2 (1 point) Monosaccharide B can be cat Сн,ОН н Дон ү0 р. Н ОН HOCH2 ОН HV СН,ОН В. Г ОН...
Use the figure below to answer the following question about glycolysis. Where did the phosphate group come from to create the second molecule shown? GLYCOLYSIS: Energy Investment Phase ATP Glucose сн,он Glucose 6-phosphate CH,OẠP Fructose 6-phosphate CH,O 2 CH2OH ADP он Кон WAO HO он HOOH OH Hexokinase VOH OH HO KOH Phosphogluco- isomerase но н ADP ATP Glycolysis Glucose Hexokinase
Ch 16.1
Give the major product(s) or the following reaction ao,a OH N ? OH io OH H There is no reaction under these conditions or the correct product is not listed here Gve the major product(s) of the following reaction COCH OH N H OH 0 OH H There is no reaction under these conditions or the correct product is not listed here. В 1) BAIH (-Bu), (-78°C) (0.5 moles) 2) ное ? оо н ОН ОН OCH, OH...
Please show all work. Will rate high!
Use the Henderson–Hasselbalch (H-H) equation to answer
the following question:
Calculate the concentration of the glutamine anion when 0.50 M of glutamine is at a physiological pH of 7.4. The pka of the a-amine group is 9.13. (Answer in mm) Match the name with the structure for each of the D-aldoses. CHO CHO но CHO H он H Но H H ОН H он HOH H он CHO но -Н H ОН но...
4.23,4.24 & 4.26 thank you
156 CHAPTER 4 Introduction to Organic Compounds Practice Problems 4.21 4.23 Draw the condensed structural formula for each of the following alkyl groups: a. propyl b. methyl 4.24 Give the correct name for each of the following substituents: a. CH CH - b. CH3CH,CHCH- c. I- 4.25 Draw the skeletal structure for each of the following compounds: a. 2,3-dimethylpentane b. 2-ethyl-1,4-dimethylcyclohexane c. 1,2-dichlorohexane 4.26 Draw the skeletal structure for each of the following compounds: a....
This question has multiple parts. Work all the parts to get the most points. Galactose has the following structure: н он HO H Но. CHO нН но Н H OH a How many chirality centers are present in this molecule? Chirality centers: 4 How many total stereoisomers does Galactose have? Stereoisomers: 16 Correct b Draw the structure of the enantiomer of Galactose. Use the wedge hash bond tools to indicate stereochemistry where it exists Oo0
1. You have given all the enzymes and intermediates in glycolysis. Choose the right enzymes and intermediates and draw the glycolytic pathway. Decorate the diagram by adding ATP, ADP, H", NADH, NAD', P, and H20 where necessary. All the steps are reversible except 1, 3 and 10; draw appropriate arrow. First arrange the reactants in the correct order. Reactants/intermediates: 3-phosphoglycerate glucose Phosphoenolpyruvate dihydroxyacetone phosphate Pyruvate glucose 6-phosphate 1,3-bisphosphoglycerate fructose 6-phosophate 2-phosphoglycerate glyceraldehyde 3-phosphate fructose 1,6-bisphosphate Enzymes: Phosphoglucoisomerase phosphoglycerate kinase phosphoglycerate...
18.
Which of the following compound(s) would undergo mutarotation in
aqueous solution?
19. Draw the chair conformation of a-D-galactopyranose.
20. Which of the following compound(s) is a glycoside?
21. Provide the reagents neccesary to carry out the following
conversion.
22. Predict the product(s) for the following reaction.
23. D-glucose & D-galactose are ______epimers of each
other.
24. Predict the product(s) for the following reaction.
25. Which of the following compound(s) would produce D-glucose
and D-mannose when treated with HCN followed...
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