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10. Convert the following 3-dimensional molecule into a Fischer projection looking along the indicated line of...
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
Solve 12-14 12. Consider the molecule shown below. OH OH f. How many stereoisomers are possible?...
Solve 12-14
12. Consider the molecule shown below. OH OH f. How many stereoisomers are possible? g. Draw each of these stereoisomers. h. Identify pairs of enantiomers and pairs of diastereomers. i. Build a model of the stereoisomer that has both OH groups pointing out. Also, build a model of the mirror image of this molecule. j. Do your two molecules represent enantiomers? Are they chiral? Fischer Projections 13. Build a model of 1-bromo-1-chloroethane. a. Draw a3D representation of this...
H 9. For each molecule: 1) Identify all possible enantiomers and distinguish those that are enantiomers, diastereomers...
H 9. For each molecule: 1) Identify all possible enantiomers and distinguish those that are enantiomers, diastereomers and meso compounds. II) Assign the absolute configuration of chiral carbons in each molecule OCH3 HO+Br HS+CN H2N-CH3 HOSH Он HO+CH3 н OCH3 Сн, ососна Br +D HOCH HC-BrHN+Br CH 8. For the following compounds, assign the absolute configuration for those with chiral carbons and identify those that are NOT enantiomers HO C-C-OHY -CCIN 13CH3 HAN CH3 CH3 осі H-CH3 H2N+CH H O+COOH...
Draw the Fischer projection of the following compound Eclipsed? IL, NOW many hydroge 10. [05 pts.]...
Draw the Fischer projection of the following compound
Eclipsed? IL, NOW many hydroge 10. [05 pts.] Draw the Fischer projection of the following compound. CHCH₂CH₂OH 1. [06 pts.] Assign the chiral center(s) as R or S for each of the follow CH3 af - Bro 3 CH₂CH₂ bound/?
3. Assign R or S configuration on all chirial centers in each of the given Fischer...
3. Assign R or S configuration on all chirial centers in each of the given Fischer projections. Then, draw the perspective drawing for each structure in the boxes below. Take particular care to indicate stereochemistry properly. 0 он HO- OCH HECH2CH2C HC Br HO H- I W OH H- a) CH₂ 6 CH₂OH OCH d) CH3 Perspective drawings:
3. Assign R or S configuration on all chirial centers in each of the given Fischer...
3. Assign R or S configuration on all chirial centers in each of the given Fischer projections. Then, draw the perspective drawing for each structure in the boxes below. Take particular care to indicate stereochemistry properly. 0 он HO- OCH HECH2CH2C HC Br HO H- I W OH H- a) CH₂ 6 CH₂OH OCH d) CH3 Perspective drawings:
1. Consider the following Fischer projection formulas of 3-amino-2-butanol. Decide which pairs of the formulas are...
1. Consider the following Fischer projection formulas of 3-amino-2-butanol. Decide which pairs of the formulas are related as enantiomers, which are related as diastereomers, and which represent identical molecules. Assign R or S absolute configuration to C2 and C3 for each structure, and then decide. List your results by letters in the spaces provided below. (5 pts) CH2CH3 O CH3CH2 - NH căH HS CH2CH3 H. NH2 SH CH3CH2CH CH,CH2 C- NH, SH Enantiomeric pairs: Diastereomeric pairs: Identical molecules:
I have completed some answers! I just really really need help with the rest! I am...
I have completed some answers! I just really really need help
with the rest! I am so lost! please help me, if you can!
What information do you need? Can you see the pictures that I
posted?
#2-6 are using the FIGURE from question #2
#7-8 go together and uses #7 FIGURE
#9-12 uses #9"s FIGURE but #11 and #12 compares the two FIGURES
from #7	
#13 and 14 are together
# 15 and # 16 are their own problems...
1) 2-amino-3-hydroxybutanoic acid 2) 2,3-dinitrobutane A. Draw the skeletal structure (line-bond) for the following compounds. B....
1) 2-amino-3-hydroxybutanoic acid
2) 2,3-dinitrobutane
A. Draw the skeletal structure (line-bond) for the following compounds. B. Convert the structures to the Most Stable and the Least Stable Newmann projections around (looking down) C2-C3 bond. (The numbering is based on the nomenclature locator numbers) C. On your skeletal structures, label the stereogenic centers (chiral carbons) if there are any. D. Draw all the possible stereoisomers for the compounds. Indicate which are enantiomer pairs. which are diastereomers to each other, and if...
please answer in multiple choice format What is the relationship between these two 23. What is...
please answer in multiple choice format
What is the relationship between these two 23. What is the relationship between these two molecules? molecules? BH BH que a. identical b. enantiomers c. diastereomers d. constitutional isomers 19. Which statement is FALSE about chiral molecules? a. Their chiral Carbons are sp hybridized. b. They have an internal plane of symmetry. c. They are optically active. d. Chiral centers are bonded to four different groups. a. enantiomers b. diastereomers c. identical d. unrelated...
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
Solve 12-14
12. Consider the molecule shown below. OH OH f. How many stereoisomers are possible? g. Draw each of these stereoisomers. h. Identify pairs of enantiomers and pairs of diastereomers. i. Build a model of the stereoisomer that has both OH groups pointing out. Also, build a model of the mirror image of this molecule. j. Do your two molecules represent enantiomers? Are they chiral? Fischer Projections 13. Build a model of 1-bromo-1-chloroethane. a. Draw a3D representation of this...
H 9. For each molecule: 1) Identify all possible enantiomers and distinguish those that are enantiomers, diastereomers and meso compounds. II) Assign the absolute configuration of chiral carbons in each molecule OCH3 HO+Br HS+CN H2N-CH3 HOSH Он HO+CH3 н OCH3 Сн, ососна Br +D HOCH HC-BrHN+Br CH 8. For the following compounds, assign the absolute configuration for those with chiral carbons and identify those that are NOT enantiomers HO C-C-OHY -CCIN 13CH3 HAN CH3 CH3 осі H-CH3 H2N+CH H O+COOH...
Draw the Fischer projection of the following compound
Eclipsed? IL, NOW many hydroge 10. [05 pts.] Draw the Fischer projection of the following compound. CHCH₂CH₂OH 1. [06 pts.] Assign the chiral center(s) as R or S for each of the follow CH3 af - Bro 3 CH₂CH₂ bound/?
3. Assign R or S configuration on all chirial centers in each of the given Fischer projections. Then, draw the perspective drawing for each structure in the boxes below. Take particular care to indicate stereochemistry properly. 0 он HO- OCH HECH2CH2C HC Br HO H- I W OH H- a) CH₂ 6 CH₂OH OCH d) CH3 Perspective drawings:
3. Assign R or S configuration on all chirial centers in each of the given Fischer projections. Then, draw the perspective drawing for each structure in the boxes below. Take particular care to indicate stereochemistry properly. 0 он HO- OCH HECH2CH2C HC Br HO H- I W OH H- a) CH₂ 6 CH₂OH OCH d) CH3 Perspective drawings:
1. Consider the following Fischer projection formulas of 3-amino-2-butanol. Decide which pairs of the formulas are related as enantiomers, which are related as diastereomers, and which represent identical molecules. Assign R or S absolute configuration to C2 and C3 for each structure, and then decide. List your results by letters in the spaces provided below. (5 pts) CH2CH3 O CH3CH2 - NH căH HS CH2CH3 H. NH2 SH CH3CH2CH CH,CH2 C- NH, SH Enantiomeric pairs: Diastereomeric pairs: Identical molecules:
I have completed some answers! I just really really need help
with the rest! I am so lost! please help me, if you can!
What information do you need? Can you see the pictures that I
posted?
#2-6 are using the FIGURE from question #2
#7-8 go together and uses #7 FIGURE
#9-12 uses #9"s FIGURE but #11 and #12 compares the two FIGURES
from #7	
#13 and 14 are together
# 15 and # 16 are their own problems...
1) 2-amino-3-hydroxybutanoic acid
2) 2,3-dinitrobutane
A. Draw the skeletal structure (line-bond) for the following compounds. B. Convert the structures to the Most Stable and the Least Stable Newmann projections around (looking down) C2-C3 bond. (The numbering is based on the nomenclature locator numbers) C. On your skeletal structures, label the stereogenic centers (chiral carbons) if there are any. D. Draw all the possible stereoisomers for the compounds. Indicate which are enantiomer pairs. which are diastereomers to each other, and if...
please answer in multiple choice format
What is the relationship between these two 23. What is the relationship between these two molecules? molecules? BH BH que a. identical b. enantiomers c. diastereomers d. constitutional isomers 19. Which statement is FALSE about chiral molecules? a. Their chiral Carbons are sp hybridized. b. They have an internal plane of symmetry. c. They are optically active. d. Chiral centers are bonded to four different groups. a. enantiomers b. diastereomers c. identical d. unrelated...
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