please help me. Draw a Fisher projection for X and assign the absolute configuration for the stereogenic center.then draw a skeletal structure of the enantiomer of X
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please help me. Draw a Fisher projection for X and
assign the absolute configuration for the...
exam prep IV. Please draw the Fisher projection for each of the following molecules and determine the absolute confi...
exam prep
IV. Please draw the Fisher projection for each of the following molecules and determine the absolute configuration (S or R) for all chirality centers. (8 pts) H3C OH C (1) H CH3 Вiн-С NO2 CH(CH3)2 (2) V. Please draw the most stable conformation of trans-1-tert-butyl-3- methylcyclohexane and cis-1-tert-butyl-3-methylcyclohexane. (6 points)
IV. Please draw the Fisher projection for each of the following molecules and determine the absolute configuration (S or R) for all chirality centers. (8 pts) H3C OH...
3. (4 points) Assign absolute configuration to each stereogenic center(s) in each molecule, draw an enantiomer...
3. (4 points) Assign absolute configuration to each stereogenic center(s) in each molecule, draw an enantiomer of each molecule, and then indicate if each molecule optically active or optically inactive. (a) (b) Он но. но- Он CHS enantiomer enantiomer
6. Draw the two chair conformations for cis-1-sec-butyl-2-ethylcyclohexane. Predict the most stable conformer and draw the...
6. Draw the two chair conformations for cis-1-sec-butyl-2-ethylcyclohexane. Predict the most stable conformer and draw the corresponding Newman projection (4 pts) 7. Convert the following compounds from their 3D structure to their Fisher projection and vice-versa (4 pts) НО Br HO co₂me HN CI CO2Me НО -СІ НЕОН СН2ОН 5| Page 8. The specific rotation for (R)-methyl 2-chloro-2,3-dihydroxypropanoate is -126.7. A student prepare a sample of methyl 2-chloro-2,3-dihydroxypropanoate enantiomers that shows a specific rotation of +89.6, (a) Calculate the percent...
For each of the following marked chiral centers, indicate the configuration (R or S). Draw the...
For each of the following marked chiral centers, indicate the configuration (R or S). Draw the enantiomer of each structure in question #1. For 1 a) and lb), draw clear 3D representations of two diasteromers for each. Draw the Fisher Projection of (2R,3MS)-2,3,4-trichlorohexane
15 uestion 25 Assign the Ror S configuration to each stereogenic center in the Fischer projection...
15 uestion 25 Assign the Ror S configuration to each stereogenic center in the Fischer projection below. CHO HTH a+H H- OH CH3 O R, S, R R, R, R OOOOO S, S, S SRS S, S, R
4. (4 points) Assign absolute configuration (R or S) to each stereogenic center of the molecules...
4. (4 points) Assign absolute configuration (R or S) to each stereogenic center of the molecules shown below CH ОН ny NH2 OH
organic chemistry. 1. please show the work (may draw this into other configuration to show) 2....
organic chemistry.
1. please show the work (may draw this into other
configuration to show)
2. please show work
CH3 H HOICH3 H3CHCH2OH HYH ΗΤΗ OH IU OH CH3 H3C 413 II HY HT CH3 Which of the Newman projections (A - E) depicted above corresponds to (S)-butan-2-ol, looking from C3-C2? Projection A Projection B Projection Projection D Projection E HO The absolute configuration of the stereogenic centre in the structure of 7-tocotrienol, shown above, is: OR OE Z None...
need help with questions 1-3 1. Assign the absolute configuration (Ror S) of the chiral points...
need help with questions 1-3
1. Assign the absolute configuration (Ror S) of the chiral points in the molecules below. 2. How many chiral carbons are in the molecule shown below? 3. Draw the molecule below in its chair form and its flipped form. Which one is more stable? Briefly explain why Br
CAN SOMEONE PLEASE ANSWER THESE FOR ME QUICKLY!!! a Assign the configuration of an alkene Draw...
CAN SOMEONE PLEASE ANSWER THESE FOR ME QUICKLY!!!
a Assign the configuration of an alkene Draw the complete mechanism of an E1 reaction Draw a reaction coordinate diagram for an E1 reaction Predict the regiochemical outcome of an E1 reaction Name: 2) For each of the reactions shown below, 8 Draw the complete mechanism of the SN1 & E1 reactions h. Draw the major product(s) of the SN1 & E1 reactions Br EtOH дон Me MeOH Chapter 8-2
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...
exam prep
IV. Please draw the Fisher projection for each of the following molecules and determine the absolute configuration (S or R) for all chirality centers. (8 pts) H3C OH C (1) H CH3 Вiн-С NO2 CH(CH3)2 (2) V. Please draw the most stable conformation of trans-1-tert-butyl-3- methylcyclohexane and cis-1-tert-butyl-3-methylcyclohexane. (6 points)
IV. Please draw the Fisher projection for each of the following molecules and determine the absolute configuration (S or R) for all chirality centers. (8 pts) H3C OH...
3. (4 points) Assign absolute configuration to each stereogenic center(s) in each molecule, draw an enantiomer of each molecule, and then indicate if each molecule optically active or optically inactive. (a) (b) Он но. но- Он CHS enantiomer enantiomer
6. Draw the two chair conformations for cis-1-sec-butyl-2-ethylcyclohexane. Predict the most stable conformer and draw the corresponding Newman projection (4 pts) 7. Convert the following compounds from their 3D structure to their Fisher projection and vice-versa (4 pts) НО Br HO co₂me HN CI CO2Me НО -СІ НЕОН СН2ОН 5| Page 8. The specific rotation for (R)-methyl 2-chloro-2,3-dihydroxypropanoate is -126.7. A student prepare a sample of methyl 2-chloro-2,3-dihydroxypropanoate enantiomers that shows a specific rotation of +89.6, (a) Calculate the percent...
For each of the following marked chiral centers, indicate the configuration (R or S). Draw the enantiomer of each structure in question #1. For 1 a) and lb), draw clear 3D representations of two diasteromers for each. Draw the Fisher Projection of (2R,3MS)-2,3,4-trichlorohexane
15 uestion 25 Assign the Ror S configuration to each stereogenic center in the Fischer projection below. CHO HTH a+H H- OH CH3 O R, S, R R, R, R OOOOO S, S, S SRS S, S, R
4. (4 points) Assign absolute configuration (R or S) to each stereogenic center of the molecules shown below CH ОН ny NH2 OH
organic chemistry.
1. please show the work (may draw this into other
configuration to show)
2. please show work
CH3 H HOICH3 H3CHCH2OH HYH ΗΤΗ OH IU OH CH3 H3C 413 II HY HT CH3 Which of the Newman projections (A - E) depicted above corresponds to (S)-butan-2-ol, looking from C3-C2? Projection A Projection B Projection Projection D Projection E HO The absolute configuration of the stereogenic centre in the structure of 7-tocotrienol, shown above, is: OR OE Z None...
need help with questions 1-3
1. Assign the absolute configuration (Ror S) of the chiral points in the molecules below. 2. How many chiral carbons are in the molecule shown below? 3. Draw the molecule below in its chair form and its flipped form. Which one is more stable? Briefly explain why Br
CAN SOMEONE PLEASE ANSWER THESE FOR ME QUICKLY!!!
a Assign the configuration of an alkene Draw the complete mechanism of an E1 reaction Draw a reaction coordinate diagram for an E1 reaction Predict the regiochemical outcome of an E1 reaction Name: 2) For each of the reactions shown below, 8 Draw the complete mechanism of the SN1 & E1 reactions h. Draw the major product(s) of the SN1 & E1 reactions Br EtOH дон Me MeOH Chapter 8-2
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...
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