Write the step by step mechanism with curved arrows of the hydrdysis of the amide in' this section.

Q: Select the answer that lists all of the carboxylic acid derivatives that Woule give a methyl ester…

A: Among the given reaction the one which would not form an methyl ester is an acid base reaction

Q: When the (R,R) isomer of the amine shown is treated with an excess of methyl iodide, then silver…

A: Step 1: When (R, R) isomer of the amine is reacted with an excess of methyl iodide and silver oxide,…

Q: Explain the products that would be formed when cholesterol is reacted with bromine in an organic…

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Q: Derry synthesizing an ester as a part of his thesis. What could be his starting material that will…

A: The target product is ester.

Q: b. Write the equation for the dissociation of ethanoic acid in solution, and explain what is…

A: The equation for the dissociation of ethanoic acid in the solution will look like,CH3COOH ↔ CH3COO-…

Q: Suggest a reasonable mechanism for the conversion of a nitrile (RCN) to the corresponding amide in…

A: Nitriles (RCN) can be converted to the corresponding amid in the presence of aqueous acid. Consider…

Q: What is reductive amination explain with example?

A: The solution is given below -

Q: likely to form when reacting Ethyl amine and excess ethyl

A: Organic reactions are those in which organic reactant react to form organic products. We have to…

Q: a) Explain why the acetamido group is an ortho, para-directing group. Why should it be less…

A: As there are two questions, we have solved the first question for you, and for the rest to be solved…

Q: Explain which amide (A, B or C) would be mainly found in the hexane layer, if there are all added to…

A: Basic rule of solubility states that like dissolves like that is polar one are mainly stays in polar…

Q: Using the mechanism for the acid-catalyzed hydrolysis of an ester as your guide, write the…

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Q: Write a curved arrow mechanism for the acid-catalyzed formation of the imine below: HO, NH2 LOH

A: Since there is a lone pair on N and partial positive charge on C attached to double bond O in…

Q: In Hinsberg's test for amines (primary, secondary and tertiary): Draw the sulfonamides produced (if…

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Q: determine the azo dye that can be formed using this amine and coupling component

A: determine the azo dye that can be formed using this amine and coupling component

Q: C3H;N2CI NANO, HCVH20 „NH2 C3H3O C3H3O C3H6 C3H6

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Q: Include a detailed arrow pushing mechanism for a reaction used to make ketamine or that ketamine…

A: At first 2-Chloro cyanobenzene undergo nucleophilic reaction with cyclopentyl magnesium bromide to…

Q: What would the reaction equate to?

A: The balanced equation for the reaction of acetic acid and NaHCO3 is,

Q: * Q. Compare and justify the easy or difficult uptake of phenol and anilline from acidic water under…

A: The answer is as follows:

Q: Write the following synthesis with the mechanism using the appropriate reagents

A: The question is based on the concept of organic reactions.   we have to convert the given reactant…

Q: the reaction time would increase if we used a mixture of dyes

A: In this question we have to explain the reaction time would increase if we used a mixture of dyes…

Q: Provide arrow pushing mechanism for this amine reaction.

A: Ans: Amines are efficiently acylated with anhydrides in presence of acetic acid , result in the…

Q: Which of the following will yield a secondary amine after reduction?

A: Given are reduction reactions.

Q: explain why sodium amide can be used to form a carbanion from a terminal alkyne but not an alkane.

A: The presence of triple bond at the end of a carbon chain is defined as terminal alkyne. Sodium amide…

Q: Explain using the ideas of bases, acids, nucleophiles and electrophiles why this reaction wouldnt…

A: This reaction does not takes place without catalyst.  Catalyst catalyses the reaction.

Q: Synthesize the following compounds using the acetoacetic ester synthesis methods. u may use any…

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Q: Write the mechanism for a  reaction of a SECONDARY AMINE with an ACID CHLORIDE to generate an AMIDE…

A:

Q: In paragraph form, provide a step-by-step experimental procedure of Benzene sulphonic acid to Phenol

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Q: In greater details and  greater explanation, describe the differences you would see when conducting…

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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: Why can a NaOH be used to distinguish amide and ammonium salts? Multiple choice 2. In the synthesis…

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Q: In greater detail and hierarchy,  describe the differences you would see when conducting propyl…

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Q: Explain and show how did the lettered compounds found in each reaction in letter a and b only. this…

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Q: please answer the question below a)what protucts would be formed  if salicin were treated with…

A: Salicin is an aryl beta-D-glucoside that is salicyl alcohol in which the phenolic hydrogen has been…

Q: Sketch a stepwise mechanism for the reaction of secondary amine with an acid chloride to generate an…

A: We have to give a mechanism for the reaction of secondary amine with an acid chloride to give amide.…

Q: Write the step by step mechanism with curved arrows of the hydrolysis of the amide in this reaction.

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Q: Draw out the mechanism with arrows for the reaction of Ubiquinone to Ubiquinol.

A: Ubiquinone or coenzyme Q is utilized as proton and carrier of the electron of a particular system…

Q: Markovnikov's Rule is needed to predict that the major substrate product in the reaction between HCI…

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Q: this is an ir of acetanilide can u please indicate the obvious functional groups

A: Acetanilide or N-phenylacetamide is an aromatic amide with a benzene ring attached to the amine…

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: The amide substituent through effects. the acidty of phenol by the negative charge of the phenoxide

A: Acid is substance which release hydrogen ions when dissolved in water and base is substance which…

Q: The amide substituent effects. the acidty of phenol by the negative charge of the phenoxide through

A: Let us discuss the acidity of phenols and effects of substituents.

Q: We saw that it is necessary to use excess amine in the reaction of an acyl chloride with an amine.…

A: It is not necessary to use excess alcohol in the reaction of an acyl chloride with an alcohol…

Q: Predict the predominant species of the compound that would be present were this hydroxy-acid is…

A: Here we are required to draw the predominant species at pH =7 .

Q: 1. Write the step by step mechanism with curved arrows of the hydrolysis of the amide in this…

A: Amide can undergo hydrolysis under acidic as well as alkaline to give acid as the final product with…

Q: For this reaction, a histidine amino acid residue acts as the general base while a lysine amino acid…

A: At first histidine residue protonates the carbonyl oxygen to increase the electrophilicity of…

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

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Amines

Amines are organic compounds with a nitrogen atom having a lone pair of electrons on it. They are derived from ammonia (NH3) wherein hydrogen atoms are substituted by an aryl or alkyl group.