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5. (a) (3pts) Look up trans-decalin and cis-decalin in your text book. Which of these is...
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...
5. (a) Convert Compound A (shown below) to its chair-like structure by placing the substituents of this compound in...
5. (a) Convert Compound A (shown below) to its chair-like structure by placing the substituents of this compound in their proper location and orientation in the decalin skeleton. (3pts for correct structure) CH3 н-о сн decalin skeleton (needs completed) Compound A (b) (i) Is the decalin skeleton shown above the cis or trans-decalin stereoisomer? (ii) Is this decalin ring able to undergo a chair-flip? (ii) Explain in two or less sentences why or why not, or draw a picture to...
Please answer both parts. Thank you :) 5. (a) Convert Compound A (shown below) to its...
Please answer both parts. Thank you :)
5. (a) Convert Compound A (shown below) to its chair-like structure by placing the substituents of this compound in their proper location and orientation in the decalin skeleton. (3pts for correct structure) CH3 HO CH₂ decalin skeleton (needs completed) Compound A (b) (i) is the decalin skeleton shown above the cis or trans-decalin stereoisomer? (ii) Is this decalin ring able to undergo a chair-flip? (iii) Explain in two or less sentences why or...
I understand part a and have it answered. I think this is a trans-decalin stereoisomer because...
I understand part a and have it answered. I think this
is a trans-decalin stereoisomer because CH3 and OH are on opposite
sides of the rings. I don't think that it can undergo a ring flip,
but I am second guessing now because one of my friends said they
thought it could. please help!!
5. (a) Convert Compound A (shown below) to its chair-like structure by placing the substituents of this compound in their proper location and orientation in the...
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...
5. Cyclohexanes can be fused together in their chair conformations in either a cis or trans...
5. Cyclohexanes can be fused together in their chair conformations in either a cis or trans fashion. (a) Count the number of axial H atoms in each structure, (b) Draw the following molecules using wedge/dash notation (all in the plane), and indicate which is cis and which is trans. но он 6. Draw both chair conformations of menthol. Circle the one with lower energy and briefly justify your choice он
Define and provide examples of the following terms: a) n-alkanes b) alkene c) alkyne d) saturated...
Define and provide examples of the following terms: a) n-alkanes b) alkene c) alkyne d) saturated e) hydrophobic f) aromatic g) hydrophilic h) combustion i) methylene group j) methyl group k) common name l) IUPAC name m) conformations n) Newman projection o) eclipsed p) staggered q) gauche conformation r) anti conformation s) catalytic cracking t) cis-trans isomers of a ring u) chair conformation v) boat conformation w) distorted boat x) half chair conformation y) axial position z) equatorial position aa)...
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...
QUESTION 19 For which one of the structures A, B, C or D given below will...
QUESTION 19 For which one of the structures A, B, C or D given below will there be no preferred conformer? Hint: It is highly recommend that you draw out both conformers when attempting this question but if you think carefully, you may rule out two structures right away... Br Bry CI СІ structure B structure C structure D structure A 1. structure A 2. structure 3. Structure D 4. Structure B QUESTION 20 1 points The structure given below...
(a) Draw the structure of the two chair forms of methylcyclohexane. Draw in all bonds (even...
(a) Draw the structure of the two chair forms of methylcyclohexane. Draw in all bonds (even the C-H bonds). Be sure the axial and equatorial bonds are shown correctly. On the appropriate structure, indicate the 1,3-diaxial interactions involving the methyl group. (b) Which is more stable, trans-1,3-dimethylcyclohexane or cis-1,3-dimethylcyclohexane? Why?
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...
5. (a) Convert Compound A (shown below) to its chair-like structure by placing the substituents of this compound in their proper location and orientation in the decalin skeleton. (3pts for correct structure) CH3 н-о сн decalin skeleton (needs completed) Compound A (b) (i) Is the decalin skeleton shown above the cis or trans-decalin stereoisomer? (ii) Is this decalin ring able to undergo a chair-flip? (ii) Explain in two or less sentences why or why not, or draw a picture to...
Please answer both parts. Thank you :)
5. (a) Convert Compound A (shown below) to its chair-like structure by placing the substituents of this compound in their proper location and orientation in the decalin skeleton. (3pts for correct structure) CH3 HO CH₂ decalin skeleton (needs completed) Compound A (b) (i) is the decalin skeleton shown above the cis or trans-decalin stereoisomer? (ii) Is this decalin ring able to undergo a chair-flip? (iii) Explain in two or less sentences why or...
I understand part a and have it answered. I think this
is a trans-decalin stereoisomer because CH3 and OH are on opposite
sides of the rings. I don't think that it can undergo a ring flip,
but I am second guessing now because one of my friends said they
thought it could. please help!!
5. (a) Convert Compound A (shown below) to its chair-like structure by placing the substituents of this compound in their proper location and orientation in the...
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...
5. Cyclohexanes can be fused together in their chair conformations in either a cis or trans fashion. (a) Count the number of axial H atoms in each structure, (b) Draw the following molecules using wedge/dash notation (all in the plane), and indicate which is cis and which is trans. но он 6. Draw both chair conformations of menthol. Circle the one with lower energy and briefly justify your choice он
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...
QUESTION 19 For which one of the structures A, B, C or D given below will there be no preferred conformer? Hint: It is highly recommend that you draw out both conformers when attempting this question but if you think carefully, you may rule out two structures right away... Br Bry CI СІ structure B structure C structure D structure A 1. structure A 2. structure 3. Structure D 4. Structure B QUESTION 20 1 points The structure given below...
(a) Draw the structure of the two chair forms of methylcyclohexane. Draw in all bonds (even the C-H bonds). Be sure the axial and equatorial bonds are shown correctly. On the appropriate structure, indicate the 1,3-diaxial interactions involving the methyl group. (b) Which is more stable, trans-1,3-dimethylcyclohexane or cis-1,3-dimethylcyclohexane? Why?
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