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. a ÇH(CH3)2a CH(CH3)2 .OH он c CH3 c CH3 B Group a: Group b:Group b: Group c: B Group c: Group a: B 1 item attempt remaining Submit Answer Try Another Version
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. CH-CH2 CI Group...
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...
of 9 Select the statement about equatorial and axial positions in cyclohexane that is correct Each face of the chair conformation of cyclohexane ring has three axial and three equatorial hydrogens in an alternating pattern. OTwo substituents on the same face of the ring that are not adjacent to each other will be trans. Two substituents on the same face of the ring, one of which is axial and one that is equatorial with be trans to each other. OEach...
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. СІ bCH2CH3 Group...
For cyclohexane indicate the changes in the positions of the axial H atoms as you change from conformation chair (A) to boat and from conformation boat (B) to mirrored chair (C). (Mark the axial hydrogen at A with a 0 and indicate its position at B and at C).
What are the substituent positions in the most stable form of the
following molecule?
#1: What are the substituent positions in the most stable form of the following molecule? A. 3 axial methyls, equatorial t-butyl B. 2 axial methyls, 1 equatorial methyl and t-butyl C. 1 axial methyl, 2 equatorial methyls and t-butyl D. Axial t-butyl, 3 equatorial methyls E. 1 axial methyl and t-butyl, 2 equatorial methyls F. 2 axial methyls and t-butyl, 1 equatorial methyl G. All substituents...
I'm confused with the ring flip
3. (10 points) chair A. The cyclohexane ring depicted below undergoes a chair-flip to form CH3 H3C H3C CH3 chair lip CHa (a) Draw the missing substituents on chair A, clearly indicating whether they are in the axial or equatorial positions. (6 points) b) Are the bromide and hydroxyl groups cis or trans to each other? (2 points) (c) Is one chair conformation energetically more stable than the other? If so, indicate which chair...