Show how you can synthesize the following tertiary amine three different ways, each using a different secondary amineand adding the final substituent by(a) reductive amination (3 ways). (b) acylation–reduction (3 ways).

Q: If a lactam (cyclic amide) contains an alkyl group with an amino group, treatment with lithium…

A: Given:

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: a) Show the mechanism of synthesis of an amide from an ester and a primary amine: b) The ester…

A:

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: b)

A: Solution -

Q: Show how Friedel–Crafts acylation might be used to synthesize the followingcompounds.  (b)…

A: Given reaction, Preparation of benzophenone by Friedel-Crafts acylation reaction.

Q: (ii). Compound B was subjected to ozonolysis, predict the product formed

A: As you already mentioned that have to solve only this question , part -(iii) so here am solving your…

Q: Give the structures of the two substrates that are required to synthesize the following drug against…

A: The molecular structure of the required drug is provided. It can be synthesized by Knorr pyrrole…

Q: Draw out a complete mechanism for imine formation from the reaction of 4-iodoaniline will be…

A: The mechanism of the reaction is as follows:

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

A:

Q: Show how Gabriel syntheses are used to prepare the following amines.(a) benzylamine

A:

Q: Explain the Mechanism - Base-Promoted Hydrolysis of an Ester to aCarboxylate Anion ?

A: In base-Promoted Hydrolysis of an Ester, there are three steps.  (i). Nucleophilic addition  (ii).…

Q: Propose a mechanism (curved arrow formalism) for the reaction of the Sulfathiuazole  to Succinyl…

A: Nucleophilic addition reaction: It is an addition reaction in which a chemical compound with an…

Q: Provide the complete mechanism using curved arrow formalism for the reaction of p-chlorobenzonitrile…

A: A. Nitrile group is -CN cyano group which under acidic hydrolysis gives carboxylic acid, -COOH.  B.…

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.

Q: Provide the complete mechanism using CAF for the reaction of aniline sequentially with (i) acetic…

A:

Q: Ketenes are highly electrophilic reagents used to prepare a variety of compounds like esters and…

A: We have been asked to give detailed mechanism for the given transformation of ketene from acid.

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

Q: 1. Answer ALL parts. a) Detail how you would use the amidomalonate synthesis to prepare a racemic…

A: To use amidomalonate synthesis to prepare a racemic mixture of leucine along with mechanism.

Q: Starting with benzene, alcohols 4 carbons or smaller and using any other reagents, propose a…

A: In this question, we want to Synthesized the given target Molecule, starting material is Benzene.

Q: Starting with acetoacetic ester and any other reagents propose a synthesis and a mechanism for the…

A: In this question, we want to Synthesized the Final Product by using Acetoacetic ester.  You can see…

Q: The compound below undergoes an intramolecular Aldol condensation reaction to form ONE MAJOR…

A: In aldol reaction when an aldehyde or ketone have alpha Hydrogen reacts with any base it gives α, β-…

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

A:

Q: How could reductive amination be used to synthesize 1-phenyl-N-methyl-1-propanamine from benzene?…

A: In a reductive amination reaction, carbonyl compound reacts with ammonia or amine to form an imine…

Q: b. Suggest mechanism for synthesis of the following cyclic ester. OH CO, Bu,N Pd(OAc),

A: Ans

Q: Propose the way that the acetophenone could be synthesize from benzene

A: Interpretation - To synthesize acetophenone from benzene.

Q: Sebatian N Compound N

A: Answer:- This question is answered by using the simple concept of chemical reactions of organic…

Q: Farnesyl pyrophosphate forms the sesquiterpene shown here. Propose a mechanism for its formation.

A: The pyrophosphate in farnesyl pyrophosphate gets cleaved by the attraction of shared pair of…

Q: Nitrobenzene undergoes sulfonation to give three disubstituted products. One of the adducts is…

A: The reaction taking place is given as,

Q: H S. NH2 H S- H3CO2C H3CO2C Nafcillin IZ

A: There are many mechanisms in organic chemistry such as nucleophilic substitution, nucleophilic…

Q: Please complete the following synthesis. via reductive amination; provide two methods. each method…

A:

Q: Which of the following compounds will react with methylamine to form the imine shown below?

A: Given as,

Q: Suggest a synthesis of the following compound by using the acetoacetic ester synthesis. Show all…

A: Target molecule

Q: The compounds commonly known as "amino acids" are actually a-aminocarboxylic acids. What carbonyl…

A: REDUCTIVE AMINATION :CONVERSION OF CARBONYL GROUP INTO AMINE  THROUGH INTERMEDIATE IMINE BY USING…

Q: d-caprolactone with 2 equivalents of ethylamine b. Use mechanism arrows to illustrate the reaction…

A:

Q: CEN ОН

A:

Q: Give the mechanism with orrect agents 9 0 Br

A:

Q: a) Provide the complete mechanism for the following reaction. Meo CH;CH2NH2 CH;OH b) Design a…

A:

Q: Treating a δ-lactone (reaction A) with ammonia yields ahydroxyamide. If a β-lactone is treated with…

A: Lactone consists an ester linkage in a cyclic ring and the carbonyl carbon is electrophilic in…

Q: Outline the mechanism of the reaction of 2 propanone with Ethanol/H+ showing the product/s that…

A:

Q: Propose a plausible mechanism for each of the following transformations.

A: A detailed mechanism explained for first three reactions are given below

Q: Show how Friedel–Crafts acylation might be used to synthesize the followingcompounds.…

A: Friedel–Crafts acylation might be used to synthesize n-butylbenzene

Q: (S)-2-Butanol, CH3CH2CHOHCH3, slowly racemizes on standing in dilute aqueous sulfuric acid.…

A: Racemization is possible only when there is breaking and making of one or more bond connecting…

Q: CEN он

A: We have given that  Propose a multistep synthesis to prepare the following compound ?