QUESTION 3 For the following molecule please draw both chair forms and submit as a file attachment to this question. Please circle the more stable chair conformation. CH3 "ОН Altach Fle Browse My Computer QUESTION 4 For this molecule (ie. the molecule above), what will be the total energy difference between the 2 chairs? QUESTION S For the following molecule please draw both chair forms and submit as a file attachment. Please circle the more stable chair CH3 Save All Answers MacBook Air 20 FS 44 F7 FS 0
QUESTION 5 For the following molecule please draw both chair forms and submit as a file attachment. Please circle the more stable chair conformation. CH 3 Attach Fle Browse My Computer QUESTION For this molecule (i.e. from above) what will be the total energy difference between the 2 chairs? Click Save and Submit to save and submit. Click Save All Answers to save all answers Save All Answers MacBook Air 20 F 44 F7 11 F 0
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QUESTION For the following molecule please draw both chair forms and submit as a file attachment ...
QUESTION 3 For the following molecule please draw both chair forms and submit as a file...
QUESTION 3 For the following molecule please draw both chair forms and submit as a file attachment to this question. Please circle the more stable chair conformation. (Please submit the answer for questions 1, 3 and 5 in one image. The answer for this question should be submitted in the answer area for question 1) CH3 OH Attach File Browse My Computer
1. For each of these molecules, draw both chair conformations. Include all the hydrogens on the...
1. For each of these molecules, draw both chair conformations. Include all the hydrogens on the ring. Circle the more stable chair conformation of each molecule. CH3 .?? H3C CH3 H3C CH3 2. Which of these two molecules is more stable, A or B? Circle your answer, and support your decision by drawing all relevant chairs.
3. a) Draw both chair conformations for the molecule shown below. (2pts) b) Circle the most...
3. a) Draw both chair conformations for the molecule shown
below. (2pts) b) Circle the most stable conformation above. Give a
brief explanation on why your choice is more stable. (2pts)
b) Circle the most stable conformation above. Give a brief
explanation on why your choice is more stable. (2pts)
3. a) Draw both chair conformations for the molecule shown below. (2pts) HO OH b) Circle the most stable conformation above. Give a brief explanation on why your choice is...
A chair conformation of compound A is shown: Answer both of the questions and explain A...
A
chair conformation of compound A is shown:
Answer both of the questions and explain
A chair conformation of Compound A is shown: CH3 ring flip H3C CH3 Conformation A a) (apts) Draw a conformation of compound A as a result of ring flip. Circle the more stable conformation if possible. b) (5pts) Draw a Newman projection of conformation A.
Chair Forms of Substituted Cyclohexanes For each structure or name below, draw both chair forms of...
Chair Forms of Substituted Cyclohexanes For each structure or name below, draw both chair forms of the compound and indicate which of the two is more stable. Consult the table of A values here. 16. 1-tert-butyl-1-methylcyclohexane Ph 19. 17. trans-1,3-dibromocyclohexane 18. Cl 20. OH
Draw each of the following compounds, including all hydrogens. Both chair forms of cis-3-isopropylcyclohexanol. Circle the...
Draw each of the following compounds, including all hydrogens. Both chair forms of cis-3-isopropylcyclohexanol. Circle the one which is more stable. (E)-3-iodo-N-i:opropyl-N-mcthylhcx-2-en-4-yn-1-amine
3. (10 pts) For each cyclohexane, draw both chair conformations and circle the conformation that is...
3. (10 pts) For each cyclohexane, draw both chair conformations and circle the conformation that is more stable (use the relative size of each substituent to determine which has more 1,3-diaxial strain) S-Bu NH2 t-Bu /25 pts
For the following pairs of isomers draw both the chair conformations. Based on your chair conformations...
For the following pairs of isomers draw both the chair conformations. Based on your chair conformations state which isomer will be more stable: Draw the most stable conformation looking down the C3-C4 bond of 4-bromo-3,6-dimethylhept-1- -3-ol in the Newman projection where C3 is the front carbon and C4 is the back carbon: Starting with the conformation you have drawing show the 5 other conformations representing 60 degree rotations of the BACK carbon in an anti-clockwise direction. For the six conformations...
Draw both chair conformations for each of the following compounds. In each case
Draw both chair conformations for each of the following compounds. In each case, identify the more stable chair conformation: (a) Methylcyclohexane (b) trans-1,2-Diisopropylcyclohexane (c) cis-1,3-Diisopropylcyclohexane (d) trans-1,4-Diisopropylcyclohexane
4.51 Draw both chair conformations for each of the following compounds. In each case, identify the...
4.51 Draw both chair conformations for each of the following compounds. In each case, identify the more stable chair conformation: (a) Methylcyclohexane (b) trans-1,2-Diisopropylcyclohexane (c) cis-1,3-Diisopropylcyclohexane (d) trans-1,4-Diisopropylcyclohexane
QUESTION 3 For the following molecule please draw both chair forms and submit as a file attachment to this question. Please circle the more stable chair conformation. (Please submit the answer for questions 1, 3 and 5 in one image. The answer for this question should be submitted in the answer area for question 1) CH3 OH Attach File Browse My Computer
1. For each of these molecules, draw both chair conformations. Include all the hydrogens on the ring. Circle the more stable chair conformation of each molecule. CH3 .?? H3C CH3 H3C CH3 2. Which of these two molecules is more stable, A or B? Circle your answer, and support your decision by drawing all relevant chairs.
3. a) Draw both chair conformations for the molecule shown
below. (2pts) b) Circle the most stable conformation above. Give a
brief explanation on why your choice is more stable. (2pts)
b) Circle the most stable conformation above. Give a brief
explanation on why your choice is more stable. (2pts)
3. a) Draw both chair conformations for the molecule shown below. (2pts) HO OH b) Circle the most stable conformation above. Give a brief explanation on why your choice is...
A
chair conformation of compound A is shown:
Answer both of the questions and explain
A chair conformation of Compound A is shown: CH3 ring flip H3C CH3 Conformation A a) (apts) Draw a conformation of compound A as a result of ring flip. Circle the more stable conformation if possible. b) (5pts) Draw a Newman projection of conformation A.
Chair Forms of Substituted Cyclohexanes For each structure or name below, draw both chair forms of the compound and indicate which of the two is more stable. Consult the table of A values here. 16. 1-tert-butyl-1-methylcyclohexane Ph 19. 17. trans-1,3-dibromocyclohexane 18. Cl 20. OH
Draw each of the following compounds, including all hydrogens. Both chair forms of cis-3-isopropylcyclohexanol. Circle the one which is more stable. (E)-3-iodo-N-i:opropyl-N-mcthylhcx-2-en-4-yn-1-amine
3. (10 pts) For each cyclohexane, draw both chair conformations and circle the conformation that is more stable (use the relative size of each substituent to determine which has more 1,3-diaxial strain) S-Bu NH2 t-Bu /25 pts
For the following pairs of isomers draw both the chair conformations. Based on your chair conformations state which isomer will be more stable: Draw the most stable conformation looking down the C3-C4 bond of 4-bromo-3,6-dimethylhept-1- -3-ol in the Newman projection where C3 is the front carbon and C4 is the back carbon: Starting with the conformation you have drawing show the 5 other conformations representing 60 degree rotations of the BACK carbon in an anti-clockwise direction. For the six conformations...
4.51 Draw both chair conformations for each of the following compounds. In each case, identify the more stable chair conformation: (a) Methylcyclohexane (b) trans-1,2-Diisopropylcyclohexane (c) cis-1,3-Diisopropylcyclohexane (d) trans-1,4-Diisopropylcyclohexane
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