8. continued Compound X, CsoH84F2, reacts with excess Hz/Pd to give a C50H88F2 compound. How many rings are in X? How ma
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8. continued Compound X, CsoH84F2, reacts with excess Hz/Pd to give a C50H88F2 compound. How many rings are in X? How ma
8. continued Compound X, CsoH84F2, reacts with excess Hz/Pd to give a C50H88F2 compound. How many rings are in X? How many double bonds are in X? Show your work. 9. Write out the mechanism for: Her CHLOH SN/ 10. For the following, use ONLY reactions we have studied in class. a) Write out 6 completely different reactions of acetophenone (reagent, product). b) Write out 3 preparations 1-methylcyclohexanol, a different starting material for each one. You may use preps where you just change the functional group, and/or preps where you have to construct the carbon chain. c) Write out 3 preparations of 2-ethoxybenzoic acid, a different starting material for each one. You may use preps where you just change the functional group, and/or preps where you have to construct the carbon chain 11. Consider this list of compounds: H CH,CN CHCwN Сн,он CH,COOH CH,COOH CHOCH, CH,CH,COOH ch,CE,CH, ch,SCH c.ਸ.ਟੈਟਸ, сн, Восн, сн, осн, сH, CH,CH,CH, CH, CH,OCH.CH CH, CHCH, bH CH, CH,OH C-HGH Which ONE of them is responsible for this IR and this NMR spectrum? IR SPECTRUM too too soo es 1600 1400 NMR SPECTRUM IR PHASE liquid film NMR SOLVENI CCl4
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