Predict the product when 3,7-diacetyl-N-ethyl phenothiazine is treated with KOtBu (2 equivalents) and methyl benzoate (2 equivalents). Show the mechanism for formation of the predicted product.
Predict the product when 3,7-diacetyl-N-ethyl phenothiazine is treated with KOtBu (2 equivalents) and methyl benzoate (2 equivalents). Show the mechanism for formation of the predicted product.
• Please show the Reaction Mechanism for the formation of 1-Ethyl 1-methyl 1-phenyl methanol (Ethyl methyl phenyl carbinol) from Ethyl Bromide. Also, discuss the following cases with plausible explanations with the possible reaction schemes. a) Formation of any by-product(s) with excess EtBr b) Formation of any Isomers c) Relative yields of the Major products if EtCl is used instead of EtBr under same reaction condition Just give brief reason(s) for your answers showing structure(s).
draw a mechanism for methyl 3 benzoate 2. For the nitration of methyl benzoate: Which product did you get? What evidence doyou have for this? Wasyourproduct pure? Whatevidence do you have for this? Explain your a. b. evidence. c. Draw the mechanism for the product you got. d. Calculate percent yield. Show your work
Write a mechanism for the nitration of methyl benzoate (major product only) Include formation of the electrophile from the reaction of nitric acid with sulfuric acid. Only one resonance structure is needed for the intermediate in the EAS portion of the mechanism
Write a reaction mechanism to show how the major mononitrated product forms when protonated methyl benzoate (a nucleophile) combines with nitronium ion (an electrophile). Use the curved-arrow formalism. Show all lone pairs and formal charges.
Write the mechanism for the formation of Malachite Green from methyl benzoate. Be sure to show all steps, including the loss of water. 1. 2. Write the mechanism for the formation of Crystal violet from diethyl carbonate. 3. Methyl benzoate is an ester, but is technically a carboxylate ester. Diethyl carbonate is a 4. Why is the green dye in this experiment called "Malachite Green"? Hint: Try looking in a 5. Write the balanced equation for the reaction of hydrochloric...
write out the mechanism for the imine formation of 2-butanone (methyl ethyl ketone) with methylamine and a catalytic amount of sulfuric acid
Show the detailed mechanism of the formation of methyl orange from 4- diazobenzenesulfonic acid and N,N-dimethylaniline. Show the detailed mechanism of the formation of methyl orange from 4-diazobenzenesulfonic acid and N, N dimethy laniline. What is the name of this mechanism? What is the name of the organic functional group formed in this reaction? What is the name of this reaction? Why does the coupling occur at the para position of the N, N-dimethylaniline? What prevents the reaction from occurring...
(References) Draw the structural formula of the principal organic product formed when ethyl benzoate is treated with H,O, NaOH, heat. • You do not have to consider stereochemistry. • You do not have to explicitly draw H atoms. . Do not include lone pairs in your answer. They will not be considered in the grading. • Include counter-ions, e.g., Nat, 1", in your submission, but draw them in their own separate sketcher. Visited not draw organic or inorganic by-products.
3. When 2-ethylcyclohexanone is treated with LDA (in the solvent THF), followed by ethyl bromide, two different alkylated products are formed. Answer the following questions about this reaction. 1) LDA THE two products 2) CH CH Br 3. a. What is LDA and what is its purpose? 3. b. Draw mechanisms for the reactions and show how the two different products are formed. Product A Mechanism Product B Mechanism 3. c. Draw an energy diagram for the formation of both...
Predict the product(s) and draw the mechanism for when the compound below are treated with excess chloroethane and AlCl3.