Which organic compound will yield the following result: methylamine, octanoic acid, or octanylamine? Why?

Q: In electrophilic aromatic substitution reaction by drawing the structures of the compounds given…

A: Electrophilic aromatic substitution :- Electrophilic aromatic substitution simply means attack of…

Q: Which of the following molecules gives a disproportionation reaction in a basic medium? A. benzyl…

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Q: What product is obtained when ethylamine reacts with excess methyl iodide in a basic solution of…

A: Please find below the reaction with mechanism.

Q: Which amines cannot be prepared by the Gabriel synthesis? Explain your choices.

A: EXPLANATION: The Gabriel Synthesis of primary amines: The Gabriel Synthesis consists of two steps…

Q: In electrophilic aromatic substitution reaction by drawing the structures of the compounds given…

A: In electrophilic aromatic substitution reaction by drawing the structures of the compounds given…

Q: please explain the reaction and mechanism of sulfide to sulfimide

A: Allylic amine is an organic compound. It is an unsaturated amine. It is colorless.

Q: Give reasons for the following:(i) Aniline does not undergo Friedal-Crafts reaction.(ii) (CH3)2 NH…

A: Friedal-Crafts reaction is an electrophillic substitution of aromatic ring with an alkyl halide and…

Q: Triethylamine is utilized as a base in organic synthesis and can form quaternary ammonium salts when…

A: To prepare triethylamine from the following starting materials: A. Ammonia B. Potassium phthalimide…

Q: n electrophilic aromatic substitution reaction by drawing the structures of the compounds given…

A: when methoxybenzene is undergoes aromatic electrophilic substitution the major product is…

Q: Maleic Acid + Bromine à racemic-2,3-Dibromosuccinic Acid Explain the mechanism and reaction

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Q: MCQ 124: Hydrogen bromide have comparatively more resistant to decomposition than A. hydrogen iodide…

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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: The heterocyclic ring in Sulfathiazole might not be stable to acid hydrolysis conditions. What…

A: Here we have to provide mechanism of hydrolysis of sulfathiazole in acidic condition-

Q: which is more basic and why? pyrazole and pyridine

A: Given,  Which is more basic and why? pyrazole and pyridine

Q: If a quaternary ammonium ion can undergo an elimination reaction with a strong base, why can’t a…

A: Quaternary ammonium ion – [N+ R4] Protonated tertiary amine ion – R3N+- H

Q: A mixture of the compounds shown below is dissolved in cyclohexane. An aqueous solution of NaOH is…

A: Given Benzoic acid Beta napthol Naphthalene

Q: The reaction that occurs when the benzaldehyde you have is reacted in a basic environment is called…

A: We have to give mechanism of cannizaro reaction and benzoin condensation

Q: Explain how the class I carbonyl

A: Since you have asked multiple question, we will solve the first question for you.If you want any…

Q: What is the main reaction mechanism for this reductive amination?

A: In given reaction sequence Nucleophilic addition and Nucleophilic substitution reaction possible.

Q: Rank the following amines based on basicity Rationalize the electronic effects responsible for the…

A: A compound can be said to be basic when it has the ability to donate its lone pair or the non-bonded…

Q: Draw structures of aniline and cyclohexylamine and use appropriate factors to compare their…

A: Please note- As per our company guidelines we are supposed to answer only one question. Kindly…

Q: How would you distinguish between methyl benzoate and phenylacetic acid using 1H NMR spectroscopy?

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Q: Describe which products will be formed as a result of the reaction with nitronium ion in the…

A: The substituents present on the benzene ring can be classified as: Activators: These increase the…

Q: What is the sulfonamide between N-methylaminobenzoic acid and benzensulfonyl chloride that will be…

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Q: What specific electrophile is attacked by benzene when it undergoes nitration?

A: Electrophile means electron-loving species or we can say the species which is deficient in electrons…

Q: Borazole  is an unusually stable cyclic compound. Propose a structure forborazole, and explain why…

A: INTRODUCTION: Borazole has the structural formula B3N3H6 is: Borazole is isoelectronic with…

Q: 2. Give the structures of compounds A and B in the following reaction scheme. 'N OMe 1. ОН /Н20 1.…

A: The reagent sodium dichromate (Na2Cr2O7) works as the oxidizing reagent. It basically oxidizes…

Q: Discuss the inductive and mesomeric (resonance) effects of the following compounds in order of…

A: Groups that have a tendency to withdraw electron towards themselves in a system are said to portray…

Q: Which of the following would you expect to dissolve in water? Explain your decision. a. butylamine…

A: The solubility of the organic compounds is majorly dependent upon their tendency and ease of…

Q: Excess ammonia must be used when a primary amine is synthesized by reductive amination. What product…

A: Synthesis of primary amine by reductive elimination takes place as follows:

Q: Come up with a reasonable mechanism to explain the following reaction.

A: Given product is a rearranged product, this we can expect only in the case of carbocation…

Q: Both pyrrole and pyridine are nitrogen containing heterocycles that are 6π Hückel aromatic. Describe…

A: Greater the percentage S character less will be the ability of donation of electron and hence less…

Q: How would you account for the following :(a) Electrophilic susbstitution in case of aromatic amines…

A: In an electrophile substitution reaction, the electrophile (E+) substitute on of the position in the…

Q: Imidazole is more basic than pyridine, but more acidic than pyrrole, why?

A: A question based on acidic and basic nature, which is to be accomplished.

Q: ) Draw the NMR spectrum you would expect from the corresponding aldehyde whose oxidation gives this…

A: As for an example of acetaldehyde when oxidizing forms acetic acid. The hydrogen of OH bond is very…

Q: + + `NH2 + CF ÑH3 + `NH2 N. CF3 ZI

A: There are two factors that govern attack of nucleophile on carbonyl carbon of unsymmetrical…

Q: The reaction of a nitrile with an alcohol in the presence of a strong acid forms an N-substituted…

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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: Although nitration of aniline is slow and gives mostly meta substitution, nitration of acetanilide…

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Q: Write the step by step mechanism with KOH, write using curved arrows of the hydrolysis of the amide,…

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Q: electrophilic aromatic displacement reaction by drawing the structures of the compounds given below…

A: Aromatic Electrophilic substitution reactions:

Q: Carboxylic acids contain carbonyl group but do not show the nucleophilic addition reaction like…

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Q: What is the outcome of the following reaction?

A: In aqueous solution, the pyranose ring would be in equilibrium with the structure of acyclic…