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- plesase help m.e with thisI. Answer questions A-C regarding the next reaction (requires more than one step) A) Analysis B) Retrosynthesis C) Synthesis. Include all the necessary reactants and the product of each of the reactions performed.What would happen after a reaction with mCPBA? What happens to the epoxides?
- When some sugars dissolve in water they spontaneously undergo changes in optical rotation called mutarrotation. The Mutarrotation of D-glucopyranose is catalyzed by acid and bases. 2-Hydroxypyridine is a more effective catalyst than phenol and pyridine for this reaction because: a.Both oxygen and N in 2-hydroxypyridine act as bases increasing the rapid interconversion of sugar b. The OH of 2-hydroxypyridine serves as the base while the current N as the acid. c. 2-hydroxypyridine acts both as a base to remove the proton from the hydroxyl group in the hemiacetal and as an acid to provide a proton to the oxygen in the hemiacetal. d.Phenol and pyridine are very expensive.chlorocyopentane may be synthesised in two different ways. fill in the missing reactant required for each pathwayHow do you get to the T2 separated from the parenthesis?
- CH3CH3OH2 can be converted into CH3CHO by?Draw 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,QIdentify the lettered intermediates in the following reaction scheme. This is an alternative method to synthesize amino acids, based on the Gabriel synthesis of 1° amines.