Please make sure to circle all non-hydrogen subtituents that are
in axil position! Thanks!
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Please make sure to circle all non-hydrogen subtituents that are
in axil position! Thanks!
4. For...
please answer all parts. your the best :) 4. For each compound below, draw the most...
please answer all parts. your the best :)
4. For each compound below, draw the most stable chair conformation. Do no draw in the hydrogen atoms. For clarity, circle all non-hydrogen substituents that are in an axial position. It may help to number the carbons in each chair first before drawing in cach substituent. (3pts for each correct conformation properly drawn) 5. (a) Convert Compound A (shown below) to its chair-like structure by placing the substituents of this compound in...
A trisubstituted cyclohexane compound is given below in its chair conformation. Draw the planar...
A trisubstituted cyclohexane compound is given below in its chair conformation. Draw the corresponding planar (overhead) representation, using wedges and hashed bonds to indicate the substituent positions. To be graded properly, include the hydrogen atoms on the chirality centers (asymmetric carbons). Be sure that both wedges/hashed bonds are drawn on the outside of the ring, or else the stereochemistry may be interpreted as square planar.
I have the answers but can you explain please ? Circle the stereoisomer that is the...
I have the answers but can you explain please ?
Circle the stereoisomer that is the more stable compound? Explain your answer by drawing the most stable chair conformer of each compound using the partial chair structures below. Your equitorial and axial substituents must be unambiguous (if they're not, please label them).
When drawing your chair structures change the applicable hydrogen atoms and leave the rest of the hydrogens present.
When drawing substituted cyclohexanes, they can be drawn in either a chair form (with axial and equatorial substituents) or in a line form (using wedges and dashes to indicate the relative positions and locations of substituents). These same types of drawings can be used to illustrate what happens after a chair flip (aka ring flip). Given the structures drawn in each part below, draw the corresponding chair conformation that would result from a chair flip.When drawing your chair structures change...
2) Draw all non-hydrogen substituents in the axial position for the following compound: он но он...
2) Draw all non-hydrogen substituents in the axial position for the following compound: он но он 3) Is the structure you drew in question No. 2 above a ß or a anomer? 4) Name the reagent that allows you to remove ethers to alcohols in sugars?
please help 4. For each pair of structures below circle the most relatively stable one. Show...
please help
4. For each pair of structures below circle the most relatively stable one. Show work by drawing relevant chair structures and/or Newman projections as needed) to clearly illustrate why. It is best practice here that only the most stable conformations for each compound are being compared in each set. For clarity. provide a few words that explain your analysis when comparing the illustrations. (12pts total for this problem) (a) ♡ va ♡ 5. (a) (3pts) Look up trans-decalin...
sodium borohydide reduction of 4 tert butylcyclohexanone. need help confirming top answers are correct and help...
sodium borohydide reduction of 4 tert
butylcyclohexanone. need help confirming top answers are correct
and help with lower section. thanks
& Draw your two products (each in the most stable chair conformation) below using the numbering provided. Show only the -OH and tert-butyl groups on the ring. a) label each group as equatorial (eq) or axial (ax). b) label each group as top face (top) or bottom face (bot). OH (ax, top) (ax, bot) .OH (Eq, top 7 (Er, top...
8 Draw your two products (each in the most stable chair conformation) below using the numbering...
8 Draw your two products (each in the most stable chair conformation) below using the numbering provided Show only the OH and terr-butyl groups on the ring a) label cach group as equatorial (eq) or axial (x). b) label each group as top face (top) or bottom face (bot). trans-4-tert-butylcyclohexanol cis 4-tert-butylcyclohexanol 9. When looking at the two compounds prepared in this reduction, which compound is more stable, cis or trans? Circle your answer. 10) Draw the most stable chair...
Using the templates provided, draw the planar representation (use wedges and dashes!) and both chair conformations...
Using the templates provided, draw the planar representation (use wedges and dashes!) and both chair conformations of the models of 1,3-dichlorocyclohexane Is one chair conformer lower in energy? If so, circle the appropriate conformation above Are the two chlorine atoms cis- or trans- to each other? Can both chlorine atoms be axial in any chair conformation? Would a solution of model A rotate plane polarized light? Why or why not? Is model A a meso compound? Model B? Model B?...
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...
please answer all parts. your the best :)
4. For each compound below, draw the most stable chair conformation. Do no draw in the hydrogen atoms. For clarity, circle all non-hydrogen substituents that are in an axial position. It may help to number the carbons in each chair first before drawing in cach substituent. (3pts for each correct conformation properly drawn) 5. (a) Convert Compound A (shown below) to its chair-like structure by placing the substituents of this compound in...
I have the answers but can you explain please ?
Circle the stereoisomer that is the more stable compound? Explain your answer by drawing the most stable chair conformer of each compound using the partial chair structures below. Your equitorial and axial substituents must be unambiguous (if they're not, please label them).
When drawing substituted cyclohexanes, they can be drawn in either a chair form (with axial and equatorial substituents) or in a line form (using wedges and dashes to indicate the relative positions and locations of substituents). These same types of drawings can be used to illustrate what happens after a chair flip (aka ring flip). Given the structures drawn in each part below, draw the corresponding chair conformation that would result from a chair flip.When drawing your chair structures change...
2) Draw all non-hydrogen substituents in the axial position for the following compound: он но он 3) Is the structure you drew in question No. 2 above a ß or a anomer? 4) Name the reagent that allows you to remove ethers to alcohols in sugars?
please help
4. For each pair of structures below circle the most relatively stable one. Show work by drawing relevant chair structures and/or Newman projections as needed) to clearly illustrate why. It is best practice here that only the most stable conformations for each compound are being compared in each set. For clarity. provide a few words that explain your analysis when comparing the illustrations. (12pts total for this problem) (a) ♡ va ♡ 5. (a) (3pts) Look up trans-decalin...
sodium borohydide reduction of 4 tert
butylcyclohexanone. need help confirming top answers are correct
and help with lower section. thanks
& Draw your two products (each in the most stable chair conformation) below using the numbering provided. Show only the -OH and tert-butyl groups on the ring. a) label each group as equatorial (eq) or axial (ax). b) label each group as top face (top) or bottom face (bot). OH (ax, top) (ax, bot) .OH (Eq, top 7 (Er, top...
8 Draw your two products (each in the most stable chair conformation) below using the numbering provided Show only the OH and terr-butyl groups on the ring a) label cach group as equatorial (eq) or axial (x). b) label each group as top face (top) or bottom face (bot). trans-4-tert-butylcyclohexanol cis 4-tert-butylcyclohexanol 9. When looking at the two compounds prepared in this reduction, which compound is more stable, cis or trans? Circle your answer. 10) Draw the most stable chair...
Using the templates provided, draw the planar representation (use wedges and dashes!) and both chair conformations of the models of 1,3-dichlorocyclohexane Is one chair conformer lower in energy? If so, circle the appropriate conformation above Are the two chlorine atoms cis- or trans- to each other? Can both chlorine atoms be axial in any chair conformation? Would a solution of model A rotate plane polarized light? Why or why not? Is model A a meso compound? Model B? Model B?...
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...
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