3. 5. Show the synthesis of the two molecules 71 any additional reagent reas require any additional reagent require OH work of boog Br + enationer enantiomer 11111 Br of crieino De N S 2 od MOZ VON 33rit P
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- provide the mechasim using the reagents shown ( asap)Explain the following result. Acetic acid (CH3COOH), labeled at its OH oxygen with theuncommon 18O isotope (shown in red), was treated with aqueous base, and then the solution was acidied. Two products having the 18O label at different locations were formed.Which reaction below give a par of diastereomers and Why?
- Give typed explanation A to DIdentify the organic functional groups and reaction type for the following reaction.The reactant is a(n)a. beta pyranoseb. beta furanosec. alpha pyranosed. alpha furanoseThe product is a(n)a. alpha furanoseb. alpha pyranosec. beta furanosed. beta pyranoseThe reaction type is:a. oxidation (benedict's)b. esterificationc. mutarotationd. reduction (hydrogenation)e. hemiacetal formationThe attached isomerization reaction, drawn using D-glucose as startingmaterial, occurs with all aldohexoses in the presence of base. Draw astepwise mechanism that illustrates how each compound is formed.
- For each of the followung reaction, determine if diasteromer A or diasreromer B forms in greater yeild explain why.the beginninf part is a benzene conntected to a O-H .OChem help... Complete the following reaction sequence: Indicate regiochemical/stereochemical details as relevant. Provide the stepwise mechanism for the following... (see image)