Q: Considering the products of your reaction between 4-aminophenol and acetic anhydride in aqueous…
A: We know that, when 4-aminophenol react with acetic anhydride then Acetylation take place on -NH2…
Q: In the preparation of sulfanilamide, why was aqueous sodium bicarbonate, rather than aqueous sodium…
A: Sulfanilamide is commonly prepared through the acetanilide route treated with chlorosulfonic acid,…
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A: When 1-naphthol is treated with any diazonium salt of benzene then orange or red dye is formed as -
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A: Answer- Camphor is a bicyclic compound it has two ring one ring present above the plane. Therefore…
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A: 2d) The addition of acid is an exothermic reaction. If the reaction vessel is not cooled, then…
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Q: 3. In which solution do you expect ethyl 4-aminobenzoate (a base) to best dissolve: water, aqueous…
A: The structure of ethyl-4-aminobenzoate is as follows: The compound contains a basic functional…
Q: Stan and Kyle have observed a reaction between the aniline derivative A and acetone. a) Stan…
A: The chemical reaction for the reaction of Aniline derivative (A) with acetone is given below.
Q: . discuss the reaction of ethanal in schiff'test. briefly explain.
A: Since you have asked multiple question, we will solve the first question for you. If you want any…
Q: In synthesizing primary (1⁰) amines by alkylation of NH3, explain how we can prevent the formation…
A: Given statement is : In synthesizing primary (1⁰) amines by alkylation of NH3, explain how we can…
Q: 1. Why is it important to make sure the amount of primary amine (sulfanilic acid) is the same as the…
A: #Q1.: Sulfanilic acid(C6H7NO3S) reacts with Dimethyl aniline(C8H11N) in the presence of sodium…
Q: Describe the differences you would see when conducting propyl amine with dimethyl amine. Be specific…
A: when conducting difference between propyl amine with dimethyl amine we will see the following…
Q: Stan and Kyle have observed a reaction between the aniline derivative A and acetone. a) Stan…
A: The boy Stan likely to be more correct. Because when aniline reacts with the acetone it will first…
Q: Explain the hofmann elimination,cope elimination and gabriel amine synthesis
A: We will Explain the hofmann elimination,cope elimination and gabriel amine synthesis one by one.
Q: 3. Explain how you would separate a mixture of 1-aminoanthracene, 1-hydoxyanthracene and anthracene…
A: The process of separation of a mixture of 1-aminoanthracene, 1-hydoxyanthracene and anthracene using…
Q: On the basis of the general mechanism for amide hydrolysis in acidic solution shown in Mechanism…
A: We wIll write mechanism of hydrolysis of Acetanilide
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A: Retrosynthetic analysis is an analysis technique try to solve the problem for the synthesis of…
Q: 14 1. Suggest a reason why this might be considered a good point for a first disconnection. II.…
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Q: On the basis of the general mechanism for acid-catalyzed ester hydrolysis shown in Mechanism 20.2,…
A: The acid hydrolysis of ethyl benzoate gives benzoic acid and ethanol as the final product. The…
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A: Para methoxy group decrease the acidity of the benzoic acid through +M effect which destabilized…
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Q: What will happen if you mix prednisone in sulphuric acid, what will be the reaction mechanism or…
A: Answer- Prednisone is a steroid. Prednisone, also known as δ1-cortisone or 1,2-dehydrocortisone or…
Q: Give the mechanism in the process of esterification. How is water formed in the reaction?
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Q: Illustrate A comparison of E2 elimination reactions using alkyl halides and amines ?
A: In case of E2 reaction, the H atom and the leaving group must be anti to each other. The products…
Q: Write the step by step mechanism with curved arrows of the hydrdysis of the amide in' this section.
A: Any organic group which has functional group CONH2 are amide
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Q: 1) Discuss three methods that can be utilised to synthesise n – heptane in the laboratory.
A: preparation n heptane ;
Q: How much excess acid was used to make the "nitrous acid" HONO that will make the diazo salt with the…
A: The amine functional group is represented as -NH2. When this group is combined with the aliphatic…
Q: Explain why a much better yield of primary amine is obtained from the reaction of an alkyl halide…
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Q: Explain how much excess acid was used to make the "nitrous acid" HONO that will make the diazo salt…
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Q: CI H;CO- -N=N- F
A: Given,
Q: Write reaction with mechanism for the isopropylation of 4-methylaniline
A: The reaction can be explained by Friedal Craft's alkylation. As in 4-methylaniline both NH2 and CH3…
Q: Fill in the blanks: A primary arylamine treated with nitrous acid is converted to a arenediazonium…
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Q: What is the predominant form of cyclohexylamine at pH 9.5? Approximately what fraction is in this…
A: In low pH, in acidic condition cyclohexyl amine gets protonated to high concentration of hydrogen…
Q: Draw the sulfonamides produced, if any, upon the addition of BSC and excess NaOH to the test…
A:
Q: What kind of reaction is the reaction between N,N-diethylaniline, and diazonium salt? Supply a…
A: This reaction is an Electrophilic aromatic substitution reaction between N, N-diethylaniline and…
Q: Give brief information about the synthesis methods of amides. Show the reaction mechanism for…
A: Amides: These are the organic compounds that consist of -CO-NH2 as a functional group. The general…
Q: Stan and Kyle have observed a reaction between the aniline derivative A and acetone. a) Stan…
A: Reaction between aniline and acetone takes place by the loss of water molecule.
Q: Draw the sulfonamides produced, if any, upon the addition of BSC and excess NaOH to the test…
A: Give in following question primary secondary and tertiary amine reaction with hinsbergs reagent and…
Q: Using aniline to perform a Friedel-Crafts acylation. However, the reaction failed and the aluminum…
A: Friedel Crafts reaction is an organic coupling reaction involving electrophilic substitution at the…
Q: Translated version of the problem: Write the obtainment of cinnamic acid (3-phenylpropenoic acid)…
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Q: In synthesizing primary (1°) amines by alkylation of NH3, explain how we can prevent the formation…
A: The formation of the secondary and tertiary amine is prevented during the preparation of amine by…
Q: d-caprolactone with 2 equivalents of ethylamine b. Use mechanism arrows to illustrate the reaction…
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Q: Benzenesulfonyl chloride or p-toluenesulfonylchloride give N-substituted sulfonamides with primary…
A: Benzenesulfonyl chloride or p-toulenesulfonyl chloride give N-substituted sulfonamides with primary…
Q: In the procedure for preparing semicarbazone derivatives, what is the pur- pose of adding sodium…
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Q: What is objective of preparation of p-Nitroaniline and illustrate with drawings.
A:
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- Give the structure of azo dye that would be formed from the given amine and coupling component.The active enantiomer of aryloxypropanolamines is the S-form, whereas the activeenantiomer of arylethanolamines is the R-form. Does this imply that the twoagents are binding differently to the binding site?In the preparation of p-Nitroaniline, there are three synthetic steps in this reaction, the first is acetylation of the amine, second is nitrates and the third is hydrolysis of the amide. Why must acetylation be done first if at all? Use chemical structures to illustrate your point.
- For extraction with ethyl-4-aminobenzoate and naphthalene using dichloromethane as the solvent, how does one separate the two compounds from one another?why is the formation of an amide from an acid chloride proceeds easily when appropriate amount of amine is added to the reaction but an amide to an acid chloride is impossibleDraw the sulfonamides produced, if any, upon the addition of BSC and excess NaOH to the test reagents used in the experiment, and then draw the corresponding products upon the addition of HCl. The experiment is "Hinsberg’s Method for Characterizing Primary, Secondary, and Tertiary Amines".
- consider the route to the Tafenoquine with respect to green chemistry priniciples what are the two instances of reaction conditions which are potentially unsuitable for further process development?Arrange the following in ascending order of reactivity for the preparation of the corresponding coumarins. Explain your answers.Why do you wash the dichloromethane solution of your reductive amination product with sodium bicarbonate, rather than dilute aqueous HCl? a) Sodium bicarbonate is a good method of removing aldehydes from organic solvent.b) The amine product will be protonated by acid and remain in the aqueous layer as a salt.c) Sodium bicarbonate transfers the amine starting material into the aqueous layer.d) Sodium bicarbonate reacts with leftover NaBH(OAc)3 and removes it from the mixture.
- Illustrate A comparison of E2 elimination reactions using alkyl halides and amines ?In synthesizing primary (1⁰) amines by alkylation of NH3, explain how we can prevent the formation of 2⁰ and 3⁰ amines as by-products? You can give an example to help you in explaining but it is not required.Write the mechanism and show the product of the reaction of 3- pentanone with n-butylamine with the molecule below with a catalytic amount of acid: