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- A hydrocarbon of unknown structure has the formula C8H10. On catalytic hydrogenation over the Lindlar catalyst, 1 equivalent of Η2 is absorbed. On hydrogenation overa palladium catalyst, 3 equivalents of Η2 are absorbed. (a) How many degrees of unsaturation are present in the unknown structure? (b) How many triple bonds are Present? (c) How many double bonds are present? (d) How many rings are present? (e) Draw a structure that fits the data.M 6 write the principal product in a, c & e and the neccesary reactives for b, d & f in the following reactions :What product is formed after 2 reactions (dilute acid then HIO4, H2SO4)?
- 19.54 Predict the major product(s) from the treatment of acetone with the following: (d) [H], (CH3)2NH, (-H2O) (e) [H], NH2NH2, (-H2O) (f) [H], NH2OH, (-H2O) (g) NaBH4, MeOH (h) RCO3H (i) HCN, KCN (j) EtMgBr followed by H₂O (k) (C6H5)3P=CHCH2CH3 (1) LIAIH, followed by H2ONeed help ASAP pls & thank you! "Provide the stable organic product(s) for the reactions below."What i sthe major product of the reduction of the following compund with LiAlH4? The correct answer is C, but please explain why.
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