1. For each of these molecules, draw both chair conformations. Include all the hydrogens on the...
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...
only need help with 2,4 and 6 QUESTION For the following molecule please draw both chair forms and submit as a file attachment to this question. You can simply draw using paper/pen, take a photo of the drawing, and submit. Please circle the more stable chair conformation CH3 CH2CH3 Attach Fle QUESTION 2 For this molecule (i.e. the molecule above), what will be the total energy difference between the 2 chairs? Round to the nearest.oo QUESTION 3 For the following...
9. (20 points) Examine the structure shown below. Draw BOTH chair conformations of this compound. SHOW ALL BONDS AND ALL HYDROGENS. Which confirmation has the lowest energy? Explain your choice in one or more complete sentence. CI CH3 H3C CH3 9. (20 points) Examine the structure shown below. Draw BOTH chair conformations of this compound. SHOW ALL BONDS AND ALL HYDROGENS. Which confirmation has the lowest energy? Explain your choice in one or more complete sentence. CI CH3 H3C CH3
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...
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.
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
9. Draw two different chair conformations of cyclohexanol, showing all hydropen atoms. Identify each position as axial or equatorial 10. Draw the most stable chair conformation of the following molecules, and estimate the amount of strain in each: (a) trans-1-Chloro-3-methylcyclohexane (b) cis-1-Ethyl-2-methylcyclohexane (c) cis-1-Bromo-4-ethylcyclohexane (d) cis-1-tert-Butylcyclohexane 11. Which isomer is more stable, cis-decalin or trans-decalin? Explain. 12. Glucose exists in two forms having a 36:64 ratio at equilibrium. Draw a skeletal structure of each, describe the difference between them and...
Provide the correct hexagonal conformation or Ring-flipped chair conformations clohexane (as parent chain) compounds. Then circle the more stable chair B-flipped chair conformations for the following Circle the more stable chair conformation. Flat Hexagon structure Chair conformation A Chair conformation B Сна Br L Br Z CH3
7. (13 points) For the compound 1-tert-butyl-4-methylcyclohexane: a. Draw the two possible chair conformations for the cis isomer, Which conformation, if either, is more stable? Circle one b. Draw the two possible chair conformations for the cis isomer, Which conformation, if either, is more stable? Circle one trans: C. Between the two more stable isomers circled above, which is more stable? Why?
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