Draw the mechanism for the acylation of N -ethyl phenothiazine using protonated acetic anhydride. Draw all reasonable structures for the sigma complex. Only show the acylation reaction on one side of phenothiazine.
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Draw the mechanism for the acylation of N -ethyl phenothiazine using protonated acetic anhydride. Draw...
will rate asap, please show all work! thank you Write the mechanism for O-acylation of vanillin with acetic anhydride in acidic conditions. Write the mechanism for O-acylation of vanillin with acetic anhydride in basic conditions.
Draw a synthesis of phenacetin that employs acetic anhydride, with mechanism.
Draw the product AND mechanism for the esterification reaction of acetic anhydride and 1-octanol (assuming there is acid catalyst present).
Questions: vide the mechanism of the synthesis of (1.) acetylferrocene, .) 1-1'diacetylferrocene from; Acetic Anhydride, Ferrocene, and ! inydride, Ferrocene, and Phosphoric Acid. Determine the % yield of 1-acetylferrocene if you st excess acetic anhydride. Acetylferrocene is the only product in this case U OT I-acetylferrocene if you started with 300 mg. of Ferrocene and Uraw structures of all starting reagents and all potential products of this reaction,
last question says draw out step by step mechanism for the formation of one of your products from Q 2 ... thats actually question 1 here. thank u!!! What major product or products would you expect from the mono-acylation of toluene assuming you used he same conditions you used for the reaction with ferrocene? What products would you find with bromobenzene? What would happen if you used a non-symmetrical anhydride, for example methyl ethyl anhydride (shown below), in the mono...
please show work. will rate Draw the mechanism for a Friedal-Craft Acylation using AICI3 as a catalyst n-Bu A. Draw the two molecu les you would use to combine to form this product using Friedal-Craft Acylation B. Draw the mechanism for the formation of the following molecule starting with your two products and /or molecules
Write a detailed mechanism for the reaction of dimethylamine in water with acetic anhydride to create N,N-dimethylacetamide which proceeds in 3 steps including proton transfer steps. Then draw curved arrows that depict electron reorganization for the mechanism step below. Arrow-pushing Instructions nno XT :0: :0 H CH3 :N-Me 1 нс N-Me Me Me
Draw the mechanism arrows for the Friedel-Crafts acylation of phenol at the ortho position. Be sure to add all lone pair electrons and nonzero formal charges. In the fourth box complete the structures and draw curved arrows between the base and first resonance structure. You do not need to add curved arrows between the resonance structures. Draw the mechanism arrows for the Friedel-Crafts acylation of phenol at the ortho position. Be sure to add all one pair electrons and nonzero...
In the mechanism for formation of acetylsalicylic acid via reaction of salicylic acid with acetic anhydride, phosphoric acid acts as a catalyst by O cleaving an acetyl group from acetic anhydride via protonation of the bridging oxygen O neutralizing the hydroxide ion side product protonating the carbonyl oxygen in the acetic anhydride protonating the phenolic oxygen of salicylic acid Question 10 (3 points) What would be the predicted major product from the thermodynamically controlled dehydration of the following material OH
Show the mechanism of the acid catalyzed reaction of an alcohol with acetic anhydride, indicating the involvement of the strong acid catalyst in the reaction. H2SO4 (cat.) R'OH ROR ROH ROD +