The limiting reagent should be NaI.
Because here multiple by iodinated products are forming.
Required to add NaI in controlled fashion to get the desired product.
What is the limiting reagent in the electrophilic aromatic substitution reaction on salicylamide.? Nal, NaOCI EtOH...
Salicylamide is another active pharmaceutical ingredient that is commonly used for pain relief. A derivative of salicyalamide can be prepared in the following electrophilic aromatic substitution reaction. Note: The combination of Nal and NaOCl generates electrophilic iodine () to be used in the EAS reaction). NH2 NH2 Nal NaOCI salicylamide mono-iodinated product Using "" as the electrophile, draw the complete mechanism for the predicted major product. Show appropriate resonance structures for the sigma complex. [3 Marks] Salicylamide is another active...
Which compound is the least reactive in the aromatic electrophilic substitution reaction? What product would you expect from the following reaction? Answer both, please. 1. Which compound is the least reactive in the aromatic electrophilic substitution reaction? NH . B NH С. SOH Logo D. NO2 E 2. What product would you expect from the following reaction? CO.CH ÇO.CH А ÇOCH B OCH, D CO.CH E
Electrophilic aromatic substitution reactions. Will someone please solve and explain every step? Aromatic Compound Reagent AlCl3 FeBr3 Substrate Product
1. Which compound is the least reactive in the aromatic electrophilic substitution reaction? A NH B. NH C. SOH D. NOZ E. Seunal volo montubong tomorú od
In an electrophilic aromatic substitution reaction, which group is both ortho, para directing and ring deactivating? Select one: -CIN 0 -NH₂ O NO₂ O-CO₂H
Why must the sodium hypochlorite in the electrophilic aromatic substitution reaction be added to the reaction mixture in ice?
Mechanism.Provide a mechanismto account for formation of the product of thefollowing Electrophilic Aromatic Substitution reaction. Mechanism. Provide a mechanism to account for formation of the product of the following Electrophilic Aromatic Substitution reaction. D. OX Reactions. Please complete the following reaction schemes. Molaro NH2 FeCl3 H300 OCH3 H2CO OCH3
250 ChemActivity 29 Electrophilic Aromatic Substitution no ChemActivity 29 Part A: Electrophilic Aromatic Substitution (What products are formed when a strong electrophile is added to benzene?) Model 1: (review) Electrophilic Addition of HCI Rani o g cyclohexene carbocation intermediate Run 2 U X benzene This product carbocation intermediate DOES NOT Critical Thinking Questions 1 For Rxn I (above) draw curved arrows showing the mechanism of electrophilic addition of HCl. Include an appropriate carbocation intermediate in the box above. Figure 1:...
Write the mechanism for an electrophilic aromatic substitution reaction given any aromatic compound and either chlorine, Cl2, or t-butyl cation as the electrophile
Reactions of aromatic compounds are: -Addition -Reduction -Electrophilic aromatic substitution -Nucleophilic aromatic substitution