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

Q: Why is only one amide obtained from the reaction of acetyl chloride with an equivalent of…

A: When acetyl chloride reacts with amine then amine act as nucleophile and attacks on carbonyl carbon…

Q: Design a synthesis for the following, using an intramolecular reaction:

A: Firstly, the reaction includes intramolecular Friedel crafts reaction resulting in the ring…

Q: 4. Draw the line angle diagram of two other functional groups that act as electrophiles in the…

A: Given information,       Functional groups that act as electrophiles in the presence of a…

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: b)Congo Red indicator is synthesized via coupling reaction of diazonium salt which is obtained by…

A: The structures of the required reactants are

Q: The BEST base for achieving -3% enolization of butanal is Select one: a. sulfuric acid b. sodium…

A: To identify the best base for only 3% enolization(partial) of butanal.

Q: Write Down the autoxidation steps of oleic- acid

A: Autooxidation is defined as the spontaneous oxidation of a substance in presence of oxygen, under…

Q: What reaction would take place if the acid chloride of m-toluic acid were mixed with water?

A: The organic reactions are carried out in more than one step. They are carried out with the help of…

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: The complete reaction of an alkyl halide towards sodium iodide in acetone results to a green flame…

A: Please repost other question, as per company policy we can solve one question at a time.

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: Why, in the last step of the mechanism for hydroxide-ion promoted hydrolysis of an amide, is the…

A: We know that the hydrolysis of an amide will yield a carboxylic acid and the base catalyst will…

Q: 1. Complete the following outlined reactions that begin with propanoic acid.

A: Solution: We know thionyl chloride is good chlorination agent. Hydroxyl group of an alcohol or…

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: Write the two acid-base equations that allow the separation of a mixture of trans-stilbene and N,…

A: Interpretation: To write the two acid-base equations that allow the separation of a mixture of…

Q: step La days of the amide in this reaction, and give Write step by mechanism with curved arrows of…

A: Amides are organic compound having general formula RCONH2.  They can undergo both acid and basic…

Q: 14 1. Suggest a reason why this might be considered a good point for a first disconnection. II.…

A: DCC is used to convert carboxylic acid to amide in the presence of the base. General reaction is…

Q: When alcohol A is heated with base as shown below, the expected epoxide does not form. Explain why…

A:

Q: Show the product formed as a result of the reaction between propanoic acid and benzyl alcohol in an…

A: The structure of propanoic acid is; The structure of benzyl alcohol is;

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

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

Q: Explain the mechanism for the acid catalyzed hydrolysis of an amide?

A: Amides are the chemical compounds that are obtained by the condensation reactions of carboxylic and…

Q: Only two of the following carbonyl-containing compounds have a large equilibrium onstant for…

A:

Q: Is the following statement true or false? If the newly added group in the tetrahedral intermediate…

A: In a nucleophilic acyl substitution reaction, the upcoming nucleophile has to be stronger base than…

Q: At pH = 12, the rate of hydrolysis of ester A is greater than the rate of hydrolysis of ester B. At…

A: Concept introduction: Catalyst: Substance which helps in increasing the rate of a particular…

Q: What product(s) would you expect from the Hofmann elimination of the following amines? If more than…

A:

Q: Give a short note on Reduction of acid chlorides ?

A: Acid chlorides are the derivatives of carboxylic acids. These are formed by the reaction of…

Q: Explain how much excess acid was used to make the "nitrous acid" HONO that will make the diazo salt…

A: The functional groups associated with a molecule are key molecular components that are responsible…

Q: Use retrosynthetic analysis to plan a synthesis of the following target molecules. The only…

A: The retrosynthetic analysis to plan a synthesis of the given molecules are to be drawn with only…

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: Obtain Nitrile by writing a primary Amide and using the required reagents

A:

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

A:

Q: a) Outline a synthetic pathway to produce N,N-dimethylaniline from benzoic acid.

A: Benzoic acid to N,N-dimethyl aniline we follow the steps given below...

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: Give 3 examples of trisubstituted epoxide and draw their structures.

A:

Q: Show the complete reaction in the synthesis of the precursor amide in the synthesis of sulfanilamide

A: Organic reactions are those in which organic reactant react with each other form organic products in…

Q: What would be the product if this compound was reacted with a base like OH?

A:

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

A:

Q: 2 How much excess acid was used to mcke the 'nitraus acid" HOND that will make the diazo salt amine?

A: Amines generally primary amines forms diazonium salt on treating with nitrous acid. And nitrous acid…

Q: a. What is the amine and coupling components of this azodye? H,CO- -N=N-

A: By seeing the structural and substitution pattern in the given azodye molecules we can decide the…

Q: What experimental means may be used to drive an esterification towards completion?

A: Esterification is the process of forming an ester from the two different reactants namely carboxylic…

Q: 1) Explain with the help of equations the function of the base in the hydrolysis of benzonitrile. C.

A: The base hydrolysis of benzonitrile produces benzoic acid.

Q: Give reasons :(a) Aniline is a weaker base than cyclohexyl amine.(b) It is difficult to prepare pure…

A: A strong base is a base that dissociates completely to give ions in solution and a weak base is a…

Q: In a benzopinacolone synthesis, if the crude product obtained at the end of the reaction has a brown…

A: Interpretation -  In a benzo pinacolone synthesis, if the crude product obtained at the end of the…

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.