Provide a reasonable disconnection (retrosynthesis ) for the following Target Molecule and complete the synthesis. Possible reagents are used for the synthesis of the target molecule Ethylacetoacetate and OEt TM Me

Q: 1. Devise a synthesis of the tripeptide sequence Phe Thr Lys using acid chloride below and…

A: The polypeptide synthesis is done as it finds huge applications in industries. To have a high yield…

Q: 2. Complete the retrosynthetic analysis of compound B. Leave FGI blank if no functional group…

A: FGI is the functional group inter conversion where one functional group is interconverted to other…

Q: Mechanism. Studies have shown that aldol condensation can be catalyzed by amines via an enamine…

A:

Q: e a plausible arrow pushing mechanism for the following transformation. Hint: hydrolysis of acetal…

A: Acetals are the functional groups that are also used as the protecting groups for certain functional…

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

A:

Q: Devise a synthesis of the tripeptide sequence Phe Thr Lys using acid chloride below and…

A:

Q: Mechanism. Studies have shown that aldol condensation can be catalyzed Propose a mechanism for the…

A: Various synthesis reactions are studied in organic chemistry. Aldol condensation is one of them. It…

Q: OMe NME2

A: In this question, we want to convert starting material to final product by using Reagents.  You can…

Q: Propose a mechanism for the hydrolysis of benzaldehyde methyl imine just shown.

A:

Q: Which of the following Phase 2 reactions is likely to target a N-bearing functional group…

A: PHASE-2 REACTION:--Phase-2- reactions occur to add hydrophilic groups to functional group of an…

Q: The macrolide shown below is the core of the antibiotic tiacumicin. Draw the primer and the…

A:

Q: Write the product that would result after subjecting benzylamine (PHCH2NH2) to the following…

A: The question is based on the concept of organic reactions.   we have to identify the Product formed…

Q: CH3 N. CH3 Но Ph

A: For retrosynthetic analysis one has to identify the compound, should have the knowledge of…

Q: Propose a mechanism for the following reaction. OPIPI Geranyl pyrophosphate

A: The given reaction is,

Q: Synthesize the following product via acetoacetic ester synthesis. Use any necessary reagents.

A:

Q: Co2+ catalyzes the hydrolysis of the lactam shown here. Propose a mechanism for the metal-ion…

A: Given reaction:

Q: ) Draw and note the similarities of the cyanohydrin anion to Vitamin B1 ylide and BMIMCl ylide…

A: Solution-

Q: Identify reagents A and B in the following reaction scheme. This synthetic sequence was used to…

A: A Gilman reagent is a diorganocopper (lithium and copper) reagent, expressed as R2CuLi, where R can…

Q: Identify M and N in the following reaction sequence, two steps in the original synthesis of the…

A: The given reaction is represented as follows:

Q: Provide such a synthesis plan for the retrosynthesis that follows. Any additional substances are…

A: We have to carry out the given retrosynthesis. The retrosynthesis is given below

Q: The mechanism of glycoside formation is the same as the second part of the mechanismfor acetal…

A:

Q: Synthesize the target molecule on the right from the starting molecule on the left. Start with a…

A:

Q: Enamines and imines are tautomers that contain N atoms. Draw a stepwise mechanism for the…

A: The first step of the acid-catalyzed conversion of enamine X to imine Y is shown as,

Q: The mechanism for drawing the products of ethyl acetoacetate reacting with: ethoxide followed by…

A: Reaction (f) is a name reaction..which known as dieckmann condensation...

Q: What effect would the nonreversible decomposition of acetoacetic acid have on the concentration of…

A: Le Chatelier's principle: This principle is used to predict the effect of a change in conditions on…

Q: The final steps in the Edman degradation result in rearrangement of a thiazolinone to an…

A: The mechanism is explained below.

Q: Propose retrosynthesis and later synthesis OCH3 OCH3

A: Retrosynthesis and synthesis are given below for following structure -

Q: 1. The total synthesis of Pironetin was accomplished using several steps we have learned this…

A: In (a), First use pyridine who acta as base and abstract proton from -OH and then -O-  will form.…

Q: Show how you will use modified Gabriel's synthesis to prepare phenylalanine in the laboratory

A: The preparation of phenylalanine using modified Gabriel's synthesis has to be shown.

Q: React the substrate with excess CH3MgBr in ether, followed by subsequent water work-up. O O

A:

Q: Provide a selective synthesis

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

Q: Complete the following multistep synthesis, depicting the possible stereochemical control in the…

A:

Q: Which of the following statements is True about disconnection in retrosynthesis. A. A disconnection…

A: Statement C is the correct answer ... i.e. A disconnection Involves a theoretical disconnection of a…

Q: 5. Using the disconnection approach propose a reasonable retrosynthetic route to accomplish the…

A: Retrosynthesis is a logical approach for designing organic synthesis involves breaking down target…

Q: b) Show a complete reaction mechanism for the synthesis of compound K via malonic ester synthesis.…

A: We need to synthesize compound K via malonic ester synthesis.  The reaction is attached in the…

Q: Synthesis route with the highest yield percentage of solefacin succinate and step by step chemical…

A: Given Synthesis route with the highest yield percentage of solefacin succinate and step by step…

Q: There are two kinds of aldolases. Class I aldolases are found in animals and plants, whereas class…

A: solution- Aldolases are often used to convert  glyceraldehyde 3-phosphate. After bringing about this…

Q: Ester group (e.g. -CO2Et)  is considered a .... Ortho/Para Directing Activator Ortho/Para Directing…

A:

Q: The enolate derived from diethyl acetamidomalonate is treated with each of the following alkyl…

A: (a) The amino acid formed on treatment of enolate derived from diethyl acetamidomalonate with given…

Q: When panacetin is added to dichloromethane and extracted with aqueous sodium bicarbonate----------…

A:

Q: Which of the following reaction is mot likely to activate a drug molecule from orally administered…

A:

Q: An imine is hydrolyzed under acidic conditions. NH H20 + NH3 (18-20) Draw the complete mechanism for…

A:

Q: OCH3

A: Here i have shown complete synthesis

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: show the mechnism of synthesis of acetoacetic ester using ethanol as starting material

A: Acetoacetic ester is formed by esterification reaction between a carboxylic acid and an alcohol in…

Q: Show experimental conditions by which to carry out the following synthesis. MeOOC Ph CHO + OMe Ph…

A: The experimental conditions by which the given synthesis occurs has to be given.

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.