On the chair conformation, the substituent at C-1 will
be
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Ans- option A
Explanation-
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On the chair conformation, the substituent at C-1 will
be
Question 12 (2 points) On the...
3. (1 pt.) Draw the most stable chair conformation for the following trisubstituted cyclohexane (write letters...
3. (1 pt.) Draw the most stable chair conformation for the following trisubstituted cyclohexane (write letters a (axial), elequatorial), d(down), u(up)) next to each substituent to indicate is position in the ring. 1112 COOH
Help Organic Chem part 4 Cyclohexane Conformations Put your model of cis-1,3-dichlorocyclohexane into a chair conformation....
Help Organic Chem part 4
Cyclohexane Conformations Put your model of cis-1,3-dichlorocyclohexane into a chair conformation. Sometimes the easiest way to do this is by adjusting it to make the axial bonds alternate up and down. Now convert it to the other chair structure, asking the instructor for help if needed. Is the second conformation still cis or is it trans? Are the two conformations the same or are they different? Draw chair structures of both conformations making sure to...
with explanation 1) Draw a chair conformation of cyclohexane. Then, draw and level properly all axial...
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...
8. (a) Redraw diagram F with an equatorial substituent X at C-1 and mark any of...
8. (a) Redraw diagram F with an equatorial substituent X at C-1 and mark any of the ring C-C bonds that are parallel or anti-periplanar to the C1-X bond. Repeat for: (i) an axial substiuent X at C-1; () an equatorial substituent X at C-2; (ii) an equatorial substituent X at C-3 6 2
Make a model of methylcyclohexane (in the chair conformation) by heir conformation he hydrogen with a...
Make a model of methylcyclohexane (in the chair conformation) by heir conformation he hydrogen with a methyl group. Convert your molecule to ano C-1 (th replacing an equatorial e methyl bearing carbon) to obtain a boat conformation, and ther flipping C-4 in the nd th opposite direction (in the direction of its equatorial hydrogen). 21. Is the methyl group in the new chair conformation equatorial or 22. Is the methyl group still on the conformation? same side of the mean...
What are the substituent positions in the most stable form of the following molecule? #1: What...
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...
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...
How would you draw the most stable conformation of trans-1-chloro-2-fluorocyclohexane? Axial chlorine on C-1, Axial fluorine...
How would you draw the most stable conformation of trans-1-chloro-2-fluorocyclohexane? Axial chlorine on C-1, Axial fluorine on C-2 Axial chlorine on C-1, Equatorial fluorine on C-2 Equatorial chlorine on C-1, Axial fluorine on C-2 Equatorial chlorine on C-1, Equatorial fluorine on C-2 Choices b and c are both correct Choices a and d are both correct Submit Answer Tries 0/1 How would you draw the most stable conformation of cis-1-ethyl-4-methylcyclohexane? Axial ethyl group on C-1, Axial methyl group on C-4...
The cyclohexane derivative shown exists primarily in the more stable of the two available chair conformations....
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...
How would you draw the most stable conformation of cis-1-ethyl-2-methylcyclohexane? Axial ethyl group on C-1, Axial...
How would you draw the most stable conformation of cis-1-ethyl-2-methylcyclohexane? Axial ethyl group on C-1, Axial methyl group on C-2 Axial ethyl group on C-1, Equatorial methyl group on C-2 Equatorial ethyl group on C-1, Axial methyl group on C-2 Equatorial ethyl group on C-1, Equatorial methyl group on C-2 Choices b and care both correct O Choices a and d are both correct Submit Answer Tries 0/1 How would you draw the most stable conformation of trans-1,4-dimethylcyclohexane? Axial methyl...
3. (1 pt.) Draw the most stable chair conformation for the following trisubstituted cyclohexane (write letters a (axial), elequatorial), d(down), u(up)) next to each substituent to indicate is position in the ring. 1112 COOH
Help Organic Chem part 4
Cyclohexane Conformations Put your model of cis-1,3-dichlorocyclohexane into a chair conformation. Sometimes the easiest way to do this is by adjusting it to make the axial bonds alternate up and down. Now convert it to the other chair structure, asking the instructor for help if needed. Is the second conformation still cis or is it trans? Are the two conformations the same or are they different? Draw chair structures of both conformations making sure to...
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...
8. (a) Redraw diagram F with an equatorial substituent X at C-1 and mark any of the ring C-C bonds that are parallel or anti-periplanar to the C1-X bond. Repeat for: (i) an axial substiuent X at C-1; () an equatorial substituent X at C-2; (ii) an equatorial substituent X at C-3 6 2
Make a model of methylcyclohexane (in the chair conformation) by heir conformation he hydrogen with a methyl group. Convert your molecule to ano C-1 (th replacing an equatorial e methyl bearing carbon) to obtain a boat conformation, and ther flipping C-4 in the nd th opposite direction (in the direction of its equatorial hydrogen). 21. Is the methyl group in the new chair conformation equatorial or 22. Is the methyl group still on the conformation? same side of the mean...
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...
How would you draw the most stable conformation of trans-1-chloro-2-fluorocyclohexane? Axial chlorine on C-1, Axial fluorine on C-2 Axial chlorine on C-1, Equatorial fluorine on C-2 Equatorial chlorine on C-1, Axial fluorine on C-2 Equatorial chlorine on C-1, Equatorial fluorine on C-2 Choices b and c are both correct Choices a and d are both correct Submit Answer Tries 0/1 How would you draw the most stable conformation of cis-1-ethyl-4-methylcyclohexane? Axial ethyl group on C-1, Axial methyl group on C-4...
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...
How would you draw the most stable conformation of cis-1-ethyl-2-methylcyclohexane? Axial ethyl group on C-1, Axial methyl group on C-2 Axial ethyl group on C-1, Equatorial methyl group on C-2 Equatorial ethyl group on C-1, Axial methyl group on C-2 Equatorial ethyl group on C-1, Equatorial methyl group on C-2 Choices b and care both correct O Choices a and d are both correct Submit Answer Tries 0/1 How would you draw the most stable conformation of trans-1,4-dimethylcyclohexane? Axial methyl...
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