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).
Remember two rules for conformational changes in cyclohexane.
1- During twisting the position of all axial group will become equitorial (only for the carbon centres where twisting is done) and vice versa.
2- The groups which are written on above the plane will remain above and the group which are below the plane will remain below the plane even after twisting.
Here in first image I m just representing the twisting or rotation to make you understand how chair is converted to boat and boat is converted to mirrored chair.Here you can see in first rotation I m just twisting carbon numbered 4,5,6 while in second rotation I m rotating carbon numbered 1,2,3.in next image I represented how hydrogens are sifting their position. Here you can clearly see in first rotation at carbon no. 4 axial 0 hydrogen above the plane is still above the plane after twisting but it has changed its position from axial to equitorial.same is the case with carbon 5 and 6 . But the position of hydrogens at 1,2,3 remains same . Similarly in second rotation we are changing hydrogen postion at 1,2,3.
Suggestion- stereochemistry is all about practice try to draw these figures 3-4 times you will become familiar with drawing conformations.
For cyclohexane indicate the changes in the positions of the axial H atoms as you change...
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...
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...
with explanation 1) Draw a chair conformation of cyclohexane. Then, draw and level properly all axial and equatorial positions on chair form of cyclohexane. 2) Draw chair, half-chair and boat conformations of ethyl cyclohexane and draw an energy diagram to explain their relative stability: 3) Draw two possible chair conformations for each of the mono-substituted cyclohexanes and determine their relative stability with proper explanation. OH 4) Draw two possible chair conformations for each of the di-substituted cyclohexanes and determine their...
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...
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
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:
(a) Given a cyclohexane framework in a chair conformation, label each position as axial (ax.) or equatorial (eq.). (b) On the same figure, label all positions that are gauche (ga.) to the Y group on carbon 1. A bin may hold more than one label.
Cyclohexane: 1.Make a boat conformation. 2.Then a chair conformation In which case are the C-H bonds on neighboring carbons eclipsing the most? 3. In which case do the H atoms on C1 and C4 approach each other most closely? 4. Based on what you saw above, which will be the most stable conformation of cyclohexane? Draw both conformations
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