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Which molecule is the most stable? Please explain.
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- 3. For the following structures: CH3a C-CH,CH3 C Hy' H (a) Determine whether each radical is a primary, secondary, or tertiary radical. (b) Rank these radicals in terms of their relative stability (1 = most stable to 3 = least stable). 4 Draw the (2) banoggata 1owhich one is the least stable to the most stable?List from most stable to least stable. Me H. Me Me Me Me H. H H. H. H. H. Me II © GMU 2020 O I, II I O III, I, II O I, II, II III, II, I O II, I, II 工エ エエ エエ
- According to the conventions above, what is the sign ( + or ) of the P.E. change (H) for Rxn 3?Are the following two structures resonance forms of each other? [6-8] no O yesQ-11. Rank these compounds from lowest to highest energy. C(CH3)3 C(CH3)3 (A) IRank the following compounds in order of decreasing stability, putting the most stable first. O B. II > I > ||| OAI>II> ||| O D. III >I> || O C. III > | > | 11 111Conformational Analysle (a) (2 pts) Circle the lower energy isomer of the two conformational loomers below. H₂C. H CH CH H₂C CH H CHs CH H H H H CH₂ bold red bond. Make sure the correct atoms are attached to the end of the bonds. Draw a Newman projection of the conformational isomer shown below looking down the H3C CHS (b) H3C₁ HO CH3 Br (c) T) For one of the reactions the molecule in (b) undergoes, the OH group and the bromine need to be anti. Draw a Newman projection of the conformation in which OH and Br are arNiteshSEE MORE QUESTIONS