monoacylation of a primary amine is far easier than diacylation. explain
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monoacylation of a primary amine is far easier than diacylation. explain
Classify each of the compounds as a primary, secondary, or tertiary amine. Primary amine Secondary amine
please answer questions 1, 2, 3, and 4. thank you. Amines 257 Questions 1. Explain the purpose of the following in this experiment: a. acetic acid b. water in step 4) c. charcoal. 2. Why is acetic anhydride a better acylating agent than acetic acid? 3. Acylations are often carried out in the presence of a base, such as a 3 amine or pyridine. What is the function of the base in these reactions? 4. Monoacylation of a primary amine...
Experimental limitations: Why is it far easier to measure e/m experimentally than either e or m individually? Note: "the numbers involved are small" is not a complete answer; while that has elements of the truth, there's a deeper reason that you should get at.
2. A reaction discussed in class involved treating a primary amine with chloroform under basic! conditions to form an isocyanide. When a secondary amine was used instead, an amide was formed: NaOH NaOH CHCIE R-NEC + CHCIE RNH2 + Lº amine RỌNH 2° amine HANR2 2. A reaction discussed in class involved treating a primary amine with chloroform under basic conditions to form an isocyanide. When a secondary amine was used instead, an amide was formed: NaOH NaOH CHCIE R-NEC...
Explain why a secondary amine forms a nitrosamine rather than a diazonium salt when it reacts with sodium nitrite and acid. R N. N=O a secondary amine a nitrosamine
Select the single best answer. Classify m-chloroaniline as a primary, secondary, or tertiary amine. O Secondary amine Tertiary amine Primary amine
When carbonyl compounds react with primary amines, an imine is usually produced while a secondary amine gives an enamine. Propose a mechanism to explain this
What is the chemical product of combining 6-Amino-2 naphthalenesulfonic acid (Primary Amine) and 2-Naphthol-6-sulfonic acid sodium salt (Activated Aromatic) along with NaNO2? It should be an Azo Dye. I think the product should show a N=N bond where one of the double benzene bonds in the Activated Aromatic was to the N from the Primary Amine, but I'm not sure where. There are 4 possible locations on the benzene double bonds of the Activated Aromatic I believe. This is what...
Hexyne is more acidic than N,N-dipropyl amine. What is the principle effect to explain this? hexyne N.N dipropyl amine A: Element Effect B: Charge Effect C: Resonance Effect D: Hybrid Orbital Effect E: Inductive Effect
Trying to figure out if it is a primary or secondary amine. what is the reading for 3369cm and 3063-3029? are they both N-H stretches? 27511 3369.6 28586 8063 8 3029.4 29180