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- Reaction a) maltose (s) + H2O (l) -----> 2 glucose (s) Reaction b) 6 CO2 (g) + 6 H2O (l) -------> glucose (s) + 6 O2 (g) How would you manipulate reactions a) and b) to ended up with the reaction c) ? Reaction c) maltose (s) + 12 O2 (g) -------> 12 CO2 (g) + 11 H2O (l)please explain the steps in the following synthesis, what is the hno2 doing to cause allopurinol? what is being done to the 4,5-diaminopyrimidine? thank you!Which of the following is the best leaving group? A) H2O B) Cl C) OH D) All are equal What type of reaction can a secondary substrate undergo? A) Both types B) Neither type C) type 1 D) type 2
- 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 reactionusing the list of reagents provided which are needed to turn the following into butanoic acid?a) Butanalb) 1-chlorobutaneplease arrange the order of letters from left to right i.e. af = CrO3 / H3O+, NaOHI. True or False ____________7] Salivary amylase can be use to hydrolyze 1,4 glycosidic bonds of cellulose.____________8] Lobry de Bruyn-van Ekenstein Transformation take place when a sugar is treated with a strongly basic reagent.
- What is the name of reaction 1? How about the name of reaction 2? a Hydrolysis b Aminolysis c Alcoholysis d Reduction Which of the following is product B? a methyl 2-bromobutanoate b 2-bromobutanoic acid c 2-bromobutanamide d 3-bromobutan-1-olWhich of the following is the best substrate for SN1 reactions? a Methyl carbon b Primary carbon c Secondary carbon d Tertiary carbonDraw the expected product of the reaction of the following sugars with excess methyliodide and silver oxide.(a) a-d-fructofuranose (b) b-d-galactopyranose
- Draw the expected product of the reaction of the following sugars with excess methyliodide and silver oxide.(a) a-d-fructofuranoseWhich substrate will you use to synthesize 1-propanol from propanal? A.) NaBH₄ B.) O₃ C.) KMnO₄ D.) CH₃MgCl E.) None of the given answerDraw the product of the reactions of succinic anhydride with each of the listed reagents. Assume in all cases that the reagent is present in excess and an aqueous workup takes place after each reaction. A. Reaction with (CH3)2CHOH. \table[[Select,Draw,Templates More,,],[/,//,I//,H,Erase]] B. Reaction with NH3. \table[[Select,Draw,tes More,Erase],[/,//,III,C,H,N,0]] Question Source: Vollhardt 7e0 Organic Chemistry: Structure And Function Publishęr: W. Freemar C. Reaction with phenylmagnesium bromide in THF, followed by H+,H2o. \table[[Select,Drav,v T,lates,,,Erase],[1,II,III,C,H,0,]] D. Reaction with LiAlH4 in ether, followed by H+,H2O \table[[Select,Draw,Templates More],[/,//,III]] \table[[3,0]] \table[[,2,Q