Can the target compound at right be efficiently synthesized from the starting material at left? Br starting material Br ? Br target If so, draw a synthesis below. If no synthesis using reagents ALEKS recognizes is possible, check the box under the drawing area. Be sure you follow the standard ALEKS rules for submitting syntheses. More... Br : ☐ T Add/Remove step X Br G Br ос E ol Ar

In a traditional method there are nine syntheses (and therefore nine antibiotic screenings) for the reactions of A1, A2, and A3 (three compounds), with B1, B2, and B3 (three compounds). However only six syntheses and screenings are necessary in the combinatorial method. Plot the number of necessary syntheses as a function of the number of compounds (assume same number of A and B) for a) the traditional (one at a time) method and b) the combinatorial method described in this lab. (Hint: start with two A and two B and continue up to ten A and ten B and then graph the results for each method

Is Lobry Van Bruyn Transformation the same as the Tautomerization of Fructose during Fehling’s test? Would Fehling’s reagent react with ketoses or is it strictly for aldoses? If yes, why do they need to tautomerize first? What would be the reaction and product when Fehling’s reagent reacts with non-reducing sugars?

Predict the locations of 14C in orotate isolated from cells grown on a small amount of uniformly labeled [14C] succinate. Justify your prediction using structural drawing.