I need help with number 1 and 2.
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I need help with number 1 and 2.
Good Average s drawn 0% 2) bond. The...
I need to know if my newman projections are labeled and drawn correctly TH rele all...
I need to know if my newman projections are labeled and drawn
correctly
TH rele all 2º carbons in the following molecule. (1 pt) 2 6-iso prop the molecule drawn below: a. Draw a Newman projection looking down the C3 to C2 bond. (2 pts) b. Draw the highest energy conformation looking down the C3-C2 bond (1 pts) Me t me B. Me H Me HO (22 6330 H 4 5 (GHS и a. Newman Projection b. Highest Energy ich...
3. (a) A bond-line (dash/wedge) structure for butane is shown below. Using the Newman projection templates...
3. (a) A bond-line (dash/wedge) structure for butane is shown below. Using the Newman projection templates provided, draw the overall lowest energy (most stable) and overall highest energy (least stable) conformation possible in Newman projection form sighting down the bond indicated. Provide a brie explanation to justify the conformer shown for cach case. (2pts each correct Newman, 2pts for valid explanation) sight down CG- bond Lowest Energy (most stable) Highest Energy (least stable) Explain: (b) For the bond-line structure below...
Pleqsw help with this question 3. (a) Consider the bond-line (dash/wedge) structure shown below. Using the...
Pleqsw help with this question
3. (a) Consider the bond-line (dash/wedge) structure shown below. Using the Newman projection templates provided to the right of this bond-line structure, draw the overall lowest energy (most stable) and overall highest energy (least stable) conformation possible in Newman projection form sighting down the C C, bond indicated. Provide a one sentence explanation to justify for the overall most stable conformation. (Ipts each correct Newman, 2pts for valid explanation) sight down Cy-- - bond .23...
1. Draw the Neman Projection of the following Promane descriptions Newman projection for most stable Newman...
1. Draw the Neman Projection of the following Promane descriptions Newman projection for most stable Newman projection for least stable conformation conformation 2. Draw the Newman projections for butane looking down the C2-C3 bond through a full 360 degree rotation. Start with the anti-staggered Newman projection then draw and label each Newman projection (staggered, eclipsed, gauche, anti-staggered, fully-eclipsed) for every 60 degrees of rotation Newman projection for most stable Newman projection for second-most stable conformation Conformation Newman projection for least...
Conformations of Alkanes and Cycloalkanes 1) Draw a Newman projection of the anni conformation of 1.2-dichloroethane...
Conformations of Alkanes and Cycloalkanes 1) Draw a Newman projection of the anni conformation of 1.2-dichloroethane che conformation of 1.2-dichloroethane 2) Draw a Newman projection of the 5) Sight along the C2-C3 bond of 2-methylbutane and draw each of the staggered conformations 4) Arrange the following conformations from lowest to highest energy. CH CH 5) Circle the Most stable conformation of the molecule shown below. н сн, YI 6) Circle the Most stable conformation of the molecule shown below.
explain how i am suppose to do these i need major help thxs!! Homework #4 Due...
explain how i am suppose to do these i need major help thxs!!
Homework #4 Due Monday March 9, 2020 Problem 1: Draw the direct Newman projections of the following molecules, along the indicated bond. Then Draw the most stable and the least stable conformation. CH3 Most Stable Least stable Direct I TOH HT XH OH CH3 Direct Most Stable Least stable OH 92 Problem V: Critical Thinking One of the formation of an epoxide in a cyclohexane is by...
I already know how to do 1 and 2. if you could show me how to...
I already know how to do 1 and 2. if you could show me how to do
number 3 on the graph above, and how to calculate the expected
energy of the conformer please
1 60 120 180 240 300 360 Torsion angle (degrees) AE (kcal/mol) In the box below each molecule, draw Newman projections for the structures A, B, and C shown from the perspective indicated. For each Newman projection that you've drawn, indicate if there are any eclipsed...
i need help with these two! Especially the first one. 13. (5 pts) How many carbon...
i need help with these two! Especially the first one.
13. (5 pts) How many carbon environments are there in trans-1,3-dimethylcyclohexane? 14. (10 points). Give a Newman projection for the view down the C2-C3 bond in the second most stable conformer of pentane. Use the standard alkyl group abbreviations (Me, Et, Pr, etc) where appropriate.
3. 1) Draw the Newman projection of the following compound, looking down the indicated bond. (2) Label this Newman...
3. 1) Draw the Newman projection of the following compound, looking down the indicated bond. (2) Label this Newman projections as a staggered or eclijpsed conformation. (3) Rotate this Newman projection to draw the Newman projection of the most stable conformation of this compound. (3) Label this Newman projections as a staggered or eclipsed conformation. (4) Re-draw this most stable conformation in a wedge-dash form as the original compound below is shown). a. он в н b. Cl
3. 1)...
I'm not even sure if I drew the structures correctly, so please double check that as...
I'm
not even sure if I drew the structures correctly, so please double
check that as well. For the first Newman projection (most stable)
are there 3 CH3 gauche groups or 6? I'm confused if I only use each
CH3 group once or twice. Thank you! Will rate quickly.
2. Calculate the barrier to rotation along the C2-C3 bond of 2.2,3,3-tetramethylbutane. Start by drawing the most stable and the least stable conformations. CHA Least stal mort statu CHう 1tl CtH3...
I need to know if my newman projections are labeled and drawn
correctly
TH rele all 2º carbons in the following molecule. (1 pt) 2 6-iso prop the molecule drawn below: a. Draw a Newman projection looking down the C3 to C2 bond. (2 pts) b. Draw the highest energy conformation looking down the C3-C2 bond (1 pts) Me t me B. Me H Me HO (22 6330 H 4 5 (GHS и a. Newman Projection b. Highest Energy ich...
3. (a) A bond-line (dash/wedge) structure for butane is shown below. Using the Newman projection templates provided, draw the overall lowest energy (most stable) and overall highest energy (least stable) conformation possible in Newman projection form sighting down the bond indicated. Provide a brie explanation to justify the conformer shown for cach case. (2pts each correct Newman, 2pts for valid explanation) sight down CG- bond Lowest Energy (most stable) Highest Energy (least stable) Explain: (b) For the bond-line structure below...
Pleqsw help with this question
3. (a) Consider the bond-line (dash/wedge) structure shown below. Using the Newman projection templates provided to the right of this bond-line structure, draw the overall lowest energy (most stable) and overall highest energy (least stable) conformation possible in Newman projection form sighting down the C C, bond indicated. Provide a one sentence explanation to justify for the overall most stable conformation. (Ipts each correct Newman, 2pts for valid explanation) sight down Cy-- - bond .23...
1. Draw the Neman Projection of the following Promane descriptions Newman projection for most stable Newman projection for least stable conformation conformation 2. Draw the Newman projections for butane looking down the C2-C3 bond through a full 360 degree rotation. Start with the anti-staggered Newman projection then draw and label each Newman projection (staggered, eclipsed, gauche, anti-staggered, fully-eclipsed) for every 60 degrees of rotation Newman projection for most stable Newman projection for second-most stable conformation Conformation Newman projection for least...
Conformations of Alkanes and Cycloalkanes 1) Draw a Newman projection of the anni conformation of 1.2-dichloroethane che conformation of 1.2-dichloroethane 2) Draw a Newman projection of the 5) Sight along the C2-C3 bond of 2-methylbutane and draw each of the staggered conformations 4) Arrange the following conformations from lowest to highest energy. CH CH 5) Circle the Most stable conformation of the molecule shown below. н сн, YI 6) Circle the Most stable conformation of the molecule shown below.
explain how i am suppose to do these i need major help thxs!!
Homework #4 Due Monday March 9, 2020 Problem 1: Draw the direct Newman projections of the following molecules, along the indicated bond. Then Draw the most stable and the least stable conformation. CH3 Most Stable Least stable Direct I TOH HT XH OH CH3 Direct Most Stable Least stable OH 92 Problem V: Critical Thinking One of the formation of an epoxide in a cyclohexane is by...
I already know how to do 1 and 2. if you could show me how to do
number 3 on the graph above, and how to calculate the expected
energy of the conformer please
1 60 120 180 240 300 360 Torsion angle (degrees) AE (kcal/mol) In the box below each molecule, draw Newman projections for the structures A, B, and C shown from the perspective indicated. For each Newman projection that you've drawn, indicate if there are any eclipsed...
i need help with these two! Especially the first one.
13. (5 pts) How many carbon environments are there in trans-1,3-dimethylcyclohexane? 14. (10 points). Give a Newman projection for the view down the C2-C3 bond in the second most stable conformer of pentane. Use the standard alkyl group abbreviations (Me, Et, Pr, etc) where appropriate.
3. 1) Draw the Newman projection of the following compound, looking down the indicated bond. (2) Label this Newman projections as a staggered or eclijpsed conformation. (3) Rotate this Newman projection to draw the Newman projection of the most stable conformation of this compound. (3) Label this Newman projections as a staggered or eclipsed conformation. (4) Re-draw this most stable conformation in a wedge-dash form as the original compound below is shown). a. он в н b. Cl
3. 1)...
I'm
not even sure if I drew the structures correctly, so please double
check that as well. For the first Newman projection (most stable)
are there 3 CH3 gauche groups or 6? I'm confused if I only use each
CH3 group once or twice. Thank you! Will rate quickly.
2. Calculate the barrier to rotation along the C2-C3 bond of 2.2,3,3-tetramethylbutane. Start by drawing the most stable and the least stable conformations. CHA Least stal mort statu CHう 1tl CtH3...
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