Which of the following compounds that has a stereoisomer that is a meso compound? DRAW THE DIAGRAM a) 1,3-dichlorocyclohexane DRAW THE DIAGRAM b) 1,2-dichlorocyclobutane DRAW THE DIAGRAM c) 1,4-dichlorocyclohexane DRAW THE DIAGRAM
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- Which of the following statement is false about conjugated systems? A conjugated system is more stable than an unconjugated A system. The s-trans isomer is favored over the s-cis isomer. A conjugated system has C multiple resonance structures. A conjugated system can only D contain two alkenes.3) Draw a cyclohexane chair with 3 substituents in the most stable conformation. Explain why the conformation you've chosen is the most stable.QUESTION 3 (a) Draw the two conformations of ethane which has an energy minimum and energy maximum using the Newman projection. Explain why one conformation is lower in energy than the other.
- 2. Draw each in its most stable conformation, clearly label which is which A) B) cis-1-chloro-2-t-butylcyclohexane cis-1-chloro-3-t-butylcyclohexane C) Which of the two compounds above is more stable?*Answer the following questions and upload your answer. A. Draw the two chair conformations of cis-1-isopropyl-3-methylcyclohexane. Write under your drawing which conformation is the most stable one. B. Would the trans isomer be more stable than the cis isomer? Why?Write the two chair conformations of each of the following and in each part designate which conformation would be more stable. Why?a) trans-1-tert-butyl-3-methylcyclohexaneb) trans-1-tert-butyl-4-methylcyclohexane
- In this question, you will draw all the constitutional isomers of CH4Br₂. This compound has an IHD of 1, which means it will either have one ring or one double bond. For this question, do not consider stereoisomers.Hello, I was reading an answer from the book Organic Chemistry by Brown et al. The question is 2.51 "Draw alternative chair conformations for each substituted cyclohexane and state which chair is more stable." There are then 4 cyclohexanes (labeled a-d). For the "a" cyclohexane, the substituents are arranged as a combination of axial and equatorial in both chair conformations. However, for the "b," "c," and "d," cyclohexanes one chair has only equatorial substituents, and the other chair has only axial substituents. Why is the "a" chair conformation different? https://www.bartleby.com/solution-answer/chapter-2-problem-251p-organic-chemistry-8th-edition/9781305580350/draw-alternative-chair-conformations-for-each-substituted-cyclohexane-and-state-which-chair-is-more/4532cd91-c341-11e9-8385-02ee952b546eIs cis-1,3-dimethylcyclohexane (total energy - 12.5020 kcal/mol) or trans-1,3-dimethylcyclohexane (total energy - 9.0056 kcal/mol) more stable? Why? Is cis-1,2-dimethylcyclohexane (total energy - 12.5020 kcal/mol) conformational isomer of trans-1,2-dimethylcyclohexane (total energy - 9.0056 kcal/mol) ? Explain your reasoning.
- 6. For each of the following, draw the most stable chair form and identify whether the more stable stereoisomer would be the cis or the trans stereoisomer? a) trans 3-tert-butyl-1-methylcyclohexane b) Cis-2-chloro-1-ethylcyclohexane c) trans-3-butyl-1-isopropylcyclohexane d) trans-4-hydroxy-1-t-butylcyclohexaneStereoisomers share the same connectivity and differ only in the way their atoms are arranged in space. Draw the structure of a compound that is a stereoisomer of cis-1,2- dibromocyclobutane. (Note that the question asks for a different stereoisomer of the named compound and not the named compound itself.) • Use the wedge/hash bond tools to indicate stereochemistry where it exists. • In cases where there is more than one answer, just draw one.Consider the compound below. a) Draw the structure showing stereochemistry, in which carbon 1 has S configuration and carbon 2 has R configuration. b) Draw the structure showing stereochemistry, in which carbons 1 and 2 have S configuration. c) are the two structures from part a and b diastereomers, identical, enantiomers, or unrelated?