Indicate the positions of the labeled groups in this molecule as axial or equatorial in the...
Indicate the positions of the labeled groups in this molecule as axial or equatorial in the most stable chair conformation. Why am I wrong???? Indicate the positions of the labeled groups in this molecule as axial or equatorial in the most stable chair conformation. a CH(CH3)2 i OH y b a CH(CH3)2 OH C CH3 cCH3 Group a: equatorial Group b: axial Group c: equatorial Group a: axial Group b: equatorial Group c: axial y An error has been detected...
Indicate the positions of the labeled groups in this molecule as axial or equatorial in the most stable chair conformation. ВОН HO CH2CH3 ACH(CH3)2 Group A: Group A: Group B: Group B:
The cyclohexane derivative shown exists primarily in the more stable of the two available chair conformations. Give the position, axial or equatorial, of each of the three groups shown in the more stable chair conformation. If a group divides its time equally between axial and equatorial positions, indicate this with ax/eq The table of "Axial Strain Energies for Monosubstituted Cyclohexanes" found in the "Strain Energy Increments" section of the Reference tool is useful for answering this question. CH-CH2 CI Group...
Is it axial, equatorial, or ax/eq? The cyclohexane derivative shown exists primarily in the more stable of the two available chair conformations. Give the position, axial or equatorial, of each of the three groups shown in the more stable chair conformation. If a group divides its time equally between axial and equatorial positions, indicate this with ax/eq. The table of "Axial Strain Energies for Monosubstituted Cyclohexanes" found in the "Strain Energy Increments" section of the Reference tool is useful for...
The cyclohexane derivative shown exists primarily in the more stable of the two available chair conformations. Give the position, axial or equatorial, of each of the three groups shown in the more stable chair conformation. If a group divides its time equally between axial and equatorial positions, indicate this with ax/eq. The table of "Axial Strain Energies for Monosubstituted Cyclohexanes" found in the "Strain Energy Increments" section of the Reference tool is useful for answering this question. The choices are...
5.5. Place the methyl groups by drawing the axial and equatorial positions on the cyclohexane structure in the chair conformations next to the cyclohexane derivatives named below. H H CH, H CH, CH, cis-1,2-Dimethylcyclohexane H CH, trans-1,2-Dimethylcyclohexane H CH, H CH, CH, eis-1,3-Dimethylcyclohexane CH, trans-1,3-Dimethylcyclohexane H H H CH, KO HC CH, cis-1,4-Dimethylcyclohexane н,с H trans-1,4-Dimethyleyclohexane
For each compound drawn below, label each OH, Br, and CH kroup as axial or equatorial. Be sure to answer all parts. Report problem Print Bro -- bH H Guided Solution с Но он 11 CH [3] HO h - H HI The axial groups in [1] are: a. OH D b. H Ос. Он а.н The equatorial groups in [1] are: а. ОН О Б . Н c. OH dH The axial groups in [2] are: e. Br D...
1. Draw the different conformations of cyclohexane and indicate which conformer is more stable and explain the reason why it is more stable. 2. Draw the saddle conformation of cyclohexane and indicate the axial and equatorial positions of the hydrogen atoms. 3. Identify the chiral carbon with an asterisk in the following molecule. Say how many stereoisomers you can have. CH3CH(OH)CH(Br)CH3
Please make hand writing neat. Thank you:) 12. Construct cis-1,3-dimethylcyclohexane by placing both -CH, groups in the axial Which is the more positions. Do ring flips and examine the two chair conformations. stable conformation? Explain your answer (12) 13. Construet trans-1,3-dimethylcyclohexane by placin g one- CH3 group axial and the other equatorial. Do ring flips and examine the two chair conformations. the more stable conformation? Explain your answer (13a). Given the two1 trans-1,3-dimethylcyclohexane and cis-1,3-dimethyleyc stable isomer? Explain your answer...
Rank the shown below in order or not Preto CH OH CH-CH2 Gad2Br -CHCH Submit Answer Try Another Version 1 item attempt remaining Indicate whether the part of much show presenter e r conformation of a compound viewed from a different perspective Tote that cis, trans isomers are an example of stereoisomers CH3 но- HO CH3 OH OH HC- -NH₂ CH3 NH2 1 item attempt remaining nswer Try Another Version