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- Rank these carbocations from the least stable cation to most.1. Estimate the relative stabilities of the 4 conformationseclipsed and eclipsed n-pentane by drawing the corresponding Newman projections in descending order according to their stability. Place the most stable or lowest energy on the left. 2. Explain what the difference in energy between the most stable and the least stable is due to. 3. What is the difference in stability between the two staggered conformations?If the elimination reaction can result in the formation of two different alkenes which one with predominate in the product?
- H. Each of the following compounds can be synthesized from an eight- carbon alkene using ozonolysis followed by dimethyl sulfide. Match the following compounds with their appropriate alkene. v Choose... H. 4-octene H. 1-methylcycloheptene cyclooctene Choose...[Review Topics] [References] Draw a structural formula for the hemiketal formed when one molecule of ethanol combines with one cyclohexanone molecule. O • You do not have to consider stereochemistry. . You do not have to explicitly draw H atoms. *a Submit Answer ... Retry Entire Group ChemDoodle 8 more group attempts remaining Previous Next Save and ExitEach of the following line structures can be described as a bicyclononane except for... OA. O B. All of these structures can be accurately described as bicyclononanes OD. OE.
- 4. Draw the preferred conformation for the following compounds. Provide a brief explanation as to why you chose that conformation. a. b. Phat vinaring og Problem 4.11/ Give the IUPAC name for each compound. moothosa. & b. C. d. bubon 2010 ai f. Problem 4.12, Give the structure corresponding to each IUPAC name. a. 1,2-dimethylcyclobutane b. 1,1,2-trimethylcyclopropane c. 4-ethyl-1,2-dimethylcyclohexane d. 1-sec-butyl-3-isopropylcyclopentane e. 1,1,2,3,4-pentamethylcycloheptane OIA3. Provide complete names for the following alkyne-containing molecules, including any R/S or E/Z descriptors. a. Br b. d. &