O Oasys Is Expected To Be Positive An Increase In Entropy Because A Cyclic Compound Is Converted Into Acyclic Compound 1 (50.77 KiB) Viewed 35 times
O Oasys Is Expected To Be Positive An Increase In Entropy Because A Cyclic Compound Is Converted Into Acyclic Compound 2 (50.37 KiB) Viewed 35 times
O OASys is expected to be positive (an increase in entropy) because a cyclic compound is converted into acyclic compound. ASys is expected to be negative (a decrease in entropy) because a cyclic compound is converted into acyclic compound. O ASys is expected to be positive (an increase in entropy) because two chemical entities are converted into one. O ASsys is expected to be negative (a decrease in entropy) because two chemical entities are converted into one. eTextbook and Media Hint Save for Later ܘܢ 5.03f Incorrect. VO O-H Attempts: 1 of 3 used Submit Answer to O AS sys is expected to be negative (a decrease in entropy) because a cyclic compound is converted into an acyclic compound. O AS sys is expected to be positive (an increase in entropy) because a cyclic compound is converted into an acyclic compound. O ASys is expected to be positive (an increase in entropy) because two molecules are converted into one molecule. O ASsys is expected to be negative (a decrease in entropy) because two molecules are converted into one molecule.
(-)-Cameroonanol has been isolated from the essential oil of Echinops giganteus (globe thistle) plants and it is associated with a strong woody fragrance. Its structure, including relative stereochemistry, was confirmed when it was made in the laboratory according to the sequence shown below (Org. Lett. 2000, 2, 2717-2719). Recall that a C-C bond is made up of one sigma bond and one pi bond. These two bonds together have a combined BDE (bond dissociation energy) of 607 kJ/mol. Use this information, together with the data in Table 6.1, to estimate the AH° for the conversion of compound 1 into compound 2. His Part 1 HBr hv * Your answer is incorrect. H The C-C double bond broken (BDE 607 kJ/mol) OC-Br formed (BDE 293 kJ/mol) C-Br formed (BDE 285 kJ/mol) OC-Br formed (BDE 272 kJ/mol) C-H broken (BDE 397 kJ/mol) C-C sigma bond broken (BDE 356 kJ/mol) C-C pi bond broken (BDE 251 kJ/mol) H-Br broken (BDE 368 kJ/mol) OC-H formed (BDE 397 kJ/mol) two steps H 3 Identify the bond(s) broken and the bond(s) formed in the reaction shown. Select all that apply. OH (-)-Cameroonanol
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