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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.Rank the leaving groups below from worst to best. -F -CH3 -Br -I -OHDraw HOCH2CH(CH3)2. Need answer fast i'll rate up
- Identify the organic functional group(s) of the reactant, the reaction type, and predict the functional group(s) of the product(s) then draw the major product(s) The reactant is:a. deoxytetroseb. alcohol pentosec. ketohexosed. aldotriosee. aldopentoseThe reaction type is:a. acetal formationb. oxidation (benedict's)c. hemiacetal formationd. acetal hydrolysise. reduction (hydrogenation)f. mutarotationThe product should be:a. alpha 1-4 disaccharideb. deoxyhexosec. carboxylic acid pentosed. alcohol pentosee. alpha pyranosef. no reaction56. If a trans alkene is reacted with OsO4 in H2S, the product is: Meso compound Hoffman product Markovnikov product Racemic mixtureIs THF a polar protic or aprotic?
