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- Rank the following groups in order of decreasing priority. −COOH, −CH2OH, −H, −CHOreactions and products for C9H8O4 C9H8O4 + O2 --> C9H8O4 + H2O --> C9H8O4 + HCl --> C9H8O4 + OH- --> C9H8O4 + Na --> C9H8O4 + F -->best condition for the reaction (1r,2s)-1 bromo-2methylcyclohexane->(s)3-methylcyclohex-1ene
- Considering both 5-methylcyclopenta-1,3-diene (A) and 7methylcyclohepta-1,3,5-triene (B), which labeled H atom is most acidic? Which labeled H atom is least acidic? Explain your choices.Can you draw the products that form when 1-butene reacts with; O3, then Me2S OsO4, then NaHSO3/H2O Br2 in H2O Please analyze in detail for each. Also can you please reply fastly?Show arrows, mechanism and product of TiCl4 + CH3-O-CH3.
- -Name the correct mechanism via arrow pushing -name each mechanism -name each minor and major products (1S,2R)-1-iodo-2-methylcyclohexane + sodium cyanide/ DMF-->Assign the stereochemical configuration (E or Z) for the alkene below. Show your work, indicating clearly which groups are assigned high priority (e.g., through assigning the groups numbers, circling only the high priority groups, or labeling groups as high or low).KMnO4, warm, conc'd reacts with hept-1-ene to yield __________. CO2, hex-1-ene CO2, hexanoic acid Formic acid, pentanoic acid Ethanoic acid, pentanal Formic acid, hexanone
- Rearrangements can occur during the dehydration of 1° alcohols eventhough no 1° carbocation is formed—that is, a 1,2-shift occurs as the C—OH2+ bond is broken, forming a more stable 2° or 3° carbocation, asshown in Equation [1]. Using this information, draw a stepwisemechanism for the reaction shown in Equation [2]. We will see anotherexample of this type of rearrangementChoose the one has the highest priority, and the one has the lowest. (Please show why) -CHO -COOH -COCH3 -CONH2Which of the following would accomplish the transformation below? a) 1. HSCH2CH2SH, H+; 2. H2, Raney Ni b) H2N-NH2, NaOH(aq), heat c) H2, Pd d) All of the above