Name the functional groups for Carbon 1 and Carbon 6 on both structures.
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Name the functional groups for Carbon 1 and Carbon 6
on both structures.
С— н 1...
6. a) List all of the organic functional groups. b) Identify all of the functional groups...
6. a) List all of the organic functional groups. b) Identify all of the functional groups in the following molecules: Me oCOMe NH он но Me Me Он Diclofenac (3) Ibuprofen (2) Aspirin (1) soNH2 oMe Ме. CF3 Rofecoxib (5) Celecoxib (4) CHOH CH2OH ON НОCH? VH но н носн.он но дно Н ОН Лонни но H ОН san Banenon H CH3 Clocobte Vanle OH CH3 CH3 Н,С CH3 দ OH CH3
14. (1 pt each) Name the following molecules. CH3 CH3 нно н н-с-с-с-NA ті Hн н,с...
14. (1 pt each) Name the following molecules. CH3 CH3 нно н н-с-с-с-NA ті Hн н,с Сн, Н CH,CH нс H 15. (3 pts each) Give the product(s) for the following reactions, and name all reactants and products. CH, он ОН н,с + нэс- сн - сн 3 нус. NH2 ОН Hн ІІ ОН + н-с-с-о-н НО P н Н ОН
4. Circle and label the functional groups in the following compounds: Hн н-с-с-о-н Hн Hн Г...
4. Circle and label the functional groups in the following compounds: Hн н-с-с-о-н Hн Hн Г N-C-H н н Hн н-с-с-с от Hн Н I-0-х O=O Hн Н | | | н-с-с-с-с 11 Н Н H О-Н Hн Hн 11 | | н-с-с-о-с-с-н | | | | Hн Hн
help me please Name Drawer # Date Identify the following as a ketose or an aldose....
help me please
Name Drawer # Date Identify the following as a ketose or an aldose. 1. о CH,он C-H C-H C O но-с-н Н-с-он но-с-н но-с —н но-с —н н-с-он но-с—н CH-он H-C-OH CH2OH CH-оH 2. Answer the following. What functional group is present in glucose? a. b. Is glucose a reducing or nonreducing carbohydrate? What should you observe when Benedict's reagant is added to glucose? Explain. c. PRE-LAB QUESTIONS 101
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...
Answer for 1a and 1b 1. Below are the cyclic and open-chain structures for glucose and...
Answer for 1a and 1b
1. Below are the cyclic and open-chain structures for glucose and fructose. (6 points total) а) Label each structure as glucose or fructose. (1 pt each, 4 pts) b) Glucose is a(n) and fructose is a(n). (ketose, aldose) (1 pt each, 2 pts) CH,OH -он HOCH ОН HOH н но/сн,он он OH H o=4 нон Но+н н+он н+он CH2OH CH2OH с=0 но-н нон н+он Сн,он
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...
11.a) Draw the open chain (Fischer) structure of D-altrose. (1pt) (b) How many chiral centers are...
11.a) Draw the open chain (Fischer) structure of D-altrose.
(1pt)
(b) How many chiral centers are in D-altrose? ______ (1pt)
(c) What is the maximum number of possible stereoisomers whch
can exist for D-altrose? _____ (1pt)
(d) Draw L-altrose in open chain form (use Fischer projection) –
you may use the space above. (1pt)
(e) Use the information above to draw a Haworth projection for
alpha-D-altropyranose. (2pt)
Ruff degradation on a monosaccharide causes C1 to be lost as
carbon dioxide,...
Please choose the correct answer: Question 1 1 pts CH-оH -о он ОН, ОН ОН The...
Please choose the correct answer:
Question 1 1 pts CH-оH -о он ОН, ОН ОН The molecular above is? alpha glucopyranose beta glucofuranose alpha fructofuranose alpha galactopyranose beta fructopyranose beta galactopyranose alpha glucofuranose beta glucopyranose Question 2 1 pts CHO Он Н OH н. н -ОН CH,он The molecule above is? galactose fructose glucose mannose ribose OOOO Question 3 1 pts СНо Н -ОН OH Н н Он CH2OH The furanose form of this molecule is which of the structures...
н'-н,о) HS Raney Ni HS H'-но) + Н Но CH2OH NH2 CI 1) LAH ОН 2)...
н'-н,о) HS Raney Ni HS H'-но) + Н Но CH2OH NH2 CI 1) LAH ОН 2) H,О ZI Question 1 (6 points). Provide IUPAC names for the following structures. Question 2 (14 points). Convert the following IUPAC names into structures. 2,4-dimethylcyclopent-2-enone 5-hydroxy-2-phenyl-3-hexanone (S)-2-bromo-2-methylcyclobutanone 3-methyl-5-(4-chlorophenyl) hexanal 3-isobutylbenzoic acid Acetic butanoic anhydride N-phenyl-N-propyl-2,3-dimethylbutanamide Page 2 o
6. a) List all of the organic functional groups. b) Identify all of the functional groups in the following molecules: Me oCOMe NH он но Me Me Он Diclofenac (3) Ibuprofen (2) Aspirin (1) soNH2 oMe Ме. CF3 Rofecoxib (5) Celecoxib (4) CHOH CH2OH ON НОCH? VH но н носн.он но дно Н ОН Лонни но H ОН san Banenon H CH3 Clocobte Vanle OH CH3 CH3 Н,С CH3 দ OH CH3
14. (1 pt each) Name the following molecules. CH3 CH3 нно н н-с-с-с-NA ті Hн н,с Сн, Н CH,CH нс H 15. (3 pts each) Give the product(s) for the following reactions, and name all reactants and products. CH, он ОН н,с + нэс- сн - сн 3 нус. NH2 ОН Hн ІІ ОН + н-с-с-о-н НО P н Н ОН
4. Circle and label the functional groups in the following compounds: Hн н-с-с-о-н Hн Hн Г N-C-H н н Hн н-с-с-с от Hн Н I-0-х O=O Hн Н | | | н-с-с-с-с 11 Н Н H О-Н Hн Hн 11 | | н-с-с-о-с-с-н | | | | Hн Hн
help me please
Name Drawer # Date Identify the following as a ketose or an aldose. 1. о CH,он C-H C-H C O но-с-н Н-с-он но-с-н но-с —н но-с —н н-с-он но-с—н CH-он H-C-OH CH2OH CH-оH 2. Answer the following. What functional group is present in glucose? a. b. Is glucose a reducing or nonreducing carbohydrate? What should you observe when Benedict's reagant is added to glucose? Explain. c. PRE-LAB QUESTIONS 101
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...
Answer for 1a and 1b
1. Below are the cyclic and open-chain structures for glucose and fructose. (6 points total) а) Label each structure as glucose or fructose. (1 pt each, 4 pts) b) Glucose is a(n) and fructose is a(n). (ketose, aldose) (1 pt each, 2 pts) CH,OH -он HOCH ОН HOH н но/сн,он он OH H o=4 нон Но+н н+он н+он CH2OH CH2OH с=0 но-н нон н+он Сн,он
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...
11.a) Draw the open chain (Fischer) structure of D-altrose.
(1pt)
(b) How many chiral centers are in D-altrose? ______ (1pt)
(c) What is the maximum number of possible stereoisomers whch
can exist for D-altrose? _____ (1pt)
(d) Draw L-altrose in open chain form (use Fischer projection) –
you may use the space above. (1pt)
(e) Use the information above to draw a Haworth projection for
alpha-D-altropyranose. (2pt)
Ruff degradation on a monosaccharide causes C1 to be lost as
carbon dioxide,...
Please choose the correct answer:
Question 1 1 pts CH-оH -о он ОН, ОН ОН The molecular above is? alpha glucopyranose beta glucofuranose alpha fructofuranose alpha galactopyranose beta fructopyranose beta galactopyranose alpha glucofuranose beta glucopyranose Question 2 1 pts CHO Он Н OH н. н -ОН CH,он The molecule above is? galactose fructose glucose mannose ribose OOOO Question 3 1 pts СНо Н -ОН OH Н н Он CH2OH The furanose form of this molecule is which of the structures...
н'-н,о) HS Raney Ni HS H'-но) + Н Но CH2OH NH2 CI 1) LAH ОН 2) H,О ZI Question 1 (6 points). Provide IUPAC names for the following structures. Question 2 (14 points). Convert the following IUPAC names into structures. 2,4-dimethylcyclopent-2-enone 5-hydroxy-2-phenyl-3-hexanone (S)-2-bromo-2-methylcyclobutanone 3-methyl-5-(4-chlorophenyl) hexanal 3-isobutylbenzoic acid Acetic butanoic anhydride N-phenyl-N-propyl-2,3-dimethylbutanamide Page 2 o
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