Homework Answers
bond
angle of a sp2 carbon is120 degree, when it is on a four
member ring, ring strain is more than, when it is on a six member
ring.
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circle the most stable of the two isomers shown below. explain your answer in two or fewer sentences 1. Circle the...
Circle the most stable and underline the least stable carbocations. 1.(1 pt each) Circle the most stable and underli...
Circle the most stable and underline the least stable
carbocations.
1.(1 pt each) Circle the most stable and underline the least stable carbocations below. 3- a.
Which conformation(s) of the two isomers A & B shown below is/are the most stable: А...
Which conformation(s) of the two isomers A & B shown below is/are the most stable: А B Me Me (a) A, with the methyl group axial (b) A, with the methyl group equatorial (c) B, with the methyl group axial (d) B, with the methyl group equatorial (e) The conformations described in (a) and (b) are equally the most stable
15. Which conformation(s) of the two isomers A & B shown below is/are the most stable:...
15. Which conformation(s) of the two isomers A & B shown below is/are the most stable: B Me Me (a) A, with the methyl group axial (b) A, with the methyl group equatorial (c) B, with the methyl group axial (d) B, with the methyl group equatorial (e) The conformations described in (a) and (b) are equally the most stable
Which, if either, of the 1,4-dimethylcyclohexane isomers shown below is more stable? Explain your answerusing depictions...
Which, if either, of the 1,4-dimethylcyclohexane isomers shown
below is more stable? Explain your answerusing depictions of the
relevant conformational equilibria.
- Which conformation(s) of the two isomers A & B shown below is/are the most stal...
- Which conformation(s) of the two isomers A & B shown below is/are the most stal A B Me Me a) A, with the methyl group axial b) A, with the methyl group equatorial c) B, with the methyl group axial d) B, with the methyl group equatorial e) The conformations described in (a) and (b) are equally the most stable
3. a) Draw both chair conformations for the molecule shown below. (2pts) b) Circle the most...
3. a) Draw both chair conformations for the molecule shown
below. (2pts) b) Circle the most stable conformation above. Give a
brief explanation on why your choice is more stable. (2pts)
b) Circle the most stable conformation above. Give a brief
explanation on why your choice is more stable. (2pts)
3. a) Draw both chair conformations for the molecule shown below. (2pts) HO OH b) Circle the most stable conformation above. Give a brief explanation on why your choice is...
Can you explain how to draw this 9(12 pts)For the two geometrical isomers of 1,2.4-trimethylkyclohexane shown,...
Can you explain how to draw this
9(12 pts)For the two geometrical isomers of 1,2.4-trimethylkyclohexane shown, answer the following a. Show the chair conformations for A b. Show the chair conformations for B c. Which isomer is the most stable (A or B)?
2. Match the following isomers Somers with the IH NMR spectrum shown below? Explain your answer....
2. Match the following isomers Somers with the IH NMR spectrum shown below? Explain your answer. mm Page 103
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...
Two isomers (A and B) of trisubstituted Cyclohexane are shown below. Are these two isomers of...
Two isomers (A and B) of trisubstituted Cyclohexane are shown below. Are these two isomers of equal energy? If so, why? Or is one more energetic than the other? If so, why? And which one? Explain in sufficient detail. To entirely illustrate your point, use drawings in addition to the ones provided.
Circle the most stable and underline the least stable
carbocations.
1.(1 pt each) Circle the most stable and underline the least stable carbocations below. 3- a.
Which conformation(s) of the two isomers A & B shown below is/are the most stable: А B Me Me (a) A, with the methyl group axial (b) A, with the methyl group equatorial (c) B, with the methyl group axial (d) B, with the methyl group equatorial (e) The conformations described in (a) and (b) are equally the most stable
15. Which conformation(s) of the two isomers A & B shown below is/are the most stable: B Me Me (a) A, with the methyl group axial (b) A, with the methyl group equatorial (c) B, with the methyl group axial (d) B, with the methyl group equatorial (e) The conformations described in (a) and (b) are equally the most stable
Which, if either, of the 1,4-dimethylcyclohexane isomers shown
below is more stable? Explain your answerusing depictions of the
relevant conformational equilibria.
- Which conformation(s) of the two isomers A & B shown below is/are the most stal A B Me Me a) A, with the methyl group axial b) A, with the methyl group equatorial c) B, with the methyl group axial d) B, with the methyl group equatorial e) The conformations described in (a) and (b) are equally the most stable
3. a) Draw both chair conformations for the molecule shown
below. (2pts) b) Circle the most stable conformation above. Give a
brief explanation on why your choice is more stable. (2pts)
b) Circle the most stable conformation above. Give a brief
explanation on why your choice is more stable. (2pts)
3. a) Draw both chair conformations for the molecule shown below. (2pts) HO OH b) Circle the most stable conformation above. Give a brief explanation on why your choice is...
Can you explain how to draw this
9(12 pts)For the two geometrical isomers of 1,2.4-trimethylkyclohexane shown, answer the following a. Show the chair conformations for A b. Show the chair conformations for B c. Which isomer is the most stable (A or B)?
2. Match the following isomers Somers with the IH NMR spectrum shown below? Explain your answer. mm Page 103
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...
Two isomers (A and B) of trisubstituted Cyclohexane are shown below. Are these two isomers of equal energy? If so, why? Or is one more energetic than the other? If so, why? And which one? Explain in sufficient detail. To entirely illustrate your point, use drawings in addition to the ones provided.
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