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A: Step 1: When (R, R) isomer of the amine is reacted with an excess of methyl iodide and silver oxide,…
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Q: Show how Fischer esterification might be used to form the following esters. In each case,suggest a…
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Q: Show how the synthetic scheme developed in synthesize this triiodobenzoic acid X-ray contrast agent.…
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Q: Identify an alternative route to acetylsalicylic acid which does not utilize ethanoic anhydride and…
A: We can prepare acetyl salicylic acid from salicylic acid and acetyl chloride.
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Q: Why is it that benzenesulfonamides of primary amines are more soluble in aqueous alkali than the…
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Q: Propose syntheses of the following derivative of diethyl malonate, of which is a starting…
A: The α-hydrogens present in diethyl malonate are very acidic which can be abstracted by a base.
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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: To show the balanced equation and for reduction of benzil by NaBH4.
Q: Briefly explain why, under aqueous acidic conditions, furan readily undergoes a reversible ring…
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Q: Write the mechanism for a reaction of a SECONDARY AMINE with an ACID CHLORIDE to generate an AMIDE…
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Q: What is the main reaction mechanism for this reductive amination?
A: In given reaction sequence Nucleophilic addition and Nucleophilic substitution reaction possible.
Q: Propose a mechanism for the coupling of acetic acid and aniline using DCC as acoupling agent
A: A first step of mechanism for the coupling of acetic acid and aniline using DCC as a coupling agent…
Q: Show how the malonic ester synthesis makes substituted acetic acids, and how theacetoacetic ester…
A: The mechanism for the malonic ester is shown below.
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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A: Quinaldic acid, also known as quinaldate or chinaldinsaeure, belongs to the class of organic…
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Q: Propose the way that the acetophenone could be synthesize from benzene
A: Interpretation - To synthesize acetophenone from benzene.
Q: Show the reaction mechanisms in converting benzophenone to benzopinacol to benzopinacolone. Why must…
A: Benzophenone when reacted with isopropyl alcohol in presence of light forms benzopinacol.…
Q: Fill in the blanks: A primary arylamine treated with nitrous acid is converted to a arenediazonium…
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Q: Give brief information about the synthesis methods of amides. Show the reaction mechanism for…
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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: Provide a full mechanism for the diazotisation of aniline.
A: In this question, we will write a complete mechanism of the formation of Diazonium salt from Aniline…
Q: Write the mechanism for each of the following reactions: a. the reaction of acetyl chloride with…
A: a) Please find below the mechanism for the reaction of acetyl chloride with water to form acetic…
Q: (a) TBSO TBSO
A: H2/Ni or Pd or Pt
Q: When o-vanillin and p-toluidine are mixed, the mixture turns to a bright orange powder as the imine…
A: We have find out the answer.
Q: Illustrate the mechanism for the prepartion of acid chlorides via thionyl chloride ?
A: Carboxylic acids are the organic compounds which contain -COOH group. Acid chlorides are the…
Q: Propose a detailed mechanism for the reaction of propanone with 1,2-ethanediol in the presence of…
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Q: What reaction sequence will form dibenylamine from benzoic acid in high yield
A: The details solution for this reaction is provided below in attach image.
Q: Outline the mechanism of the reaction of 2 propanone with Ethanol/H+ showing the product/s that…
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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: Write a detailed mechanism for oxidative dehydrogenation of isobutyric acid to methacrylic acid.
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Suggest a reasonable mechanism for the conversion of a nitrile (RCN) to the corresponding amide in aqueous acid.
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- Show how to synthesize the following amines from the indicated starting materials byreductive amination.(a) benzylmethylamine from benzaldehyde(D)The best route to synthesise aromatic primary amines is by reduction of the corresponding nitro compounds. Draw the reaction scheme for the preparation of p-toluidine.Synthesis of amides from acid chlorides is an effective tool for creating many different compounds. One such compound is DEET, a.k.a. (N,N)-Diethyl-m-toluamide, a powerful insect repellent. Propose a chemical synthesis of DEET from m-toluic acid and any other necessary reagents. Provide a literature reference for any reaction that is not common knowledge.
- Benzenesulfonyl chloride or p-toluenesulfonylchloride give N-substituted sulfonamides with primary and secondary amines. The derivative consisting of primary amines is insoluble in dilute NaOH. Is that true or false?Primary amines can also be prepared by the reaction of an alkyl halide with azide ion, followed by catalytic hydrogenation. What advantage do this method and the Gabriel synthesis have over the synthesis of a primaryamine using an alkyl halide and ammonia?please explain the reaction and mechanism of sulfide to sulfimide and from sulfimide to allylic amine
- Write mechanisms for the reactions of aniline with acetyl chloride and with acetic acid, to give acetanilide.Show how you would accomplish the following syntheses using amides as intermediates.You may use any necessary reagents.(a) benzoic acid S benzyldimethylamineOn the basis of the general mechanism for amide hydrolysis in acidic solution shown in Mechanism 20.4, write an analogous sequence of steps for the hydrolysis of acetanilide.
- Benzenesulfonyl chloride or p-toluenesulfonylchloride give N-substituted sulfonamides with primary and secondary amines. The derivative consisting of primary amines is insoluble in dilute NaOH.RightFalsewhy 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 impossiblePropose syntheses of the following derivative of diethyl malonate, of which is a starting material for synthesis of a barbiturate.