Give a reduction that you can use to synthesize benzaldehyde.

Q: Please help me find the reagents of the synthesis

A: To solve this problem we have to do following steps (1) alkyne is treated with NaNH2 to form a ionic…

Q: Match each step with the description that best fits it. a)proton transfer b)nucleophilic attack…

A: Each step of reaction with following description are

Q: the

A: The reaction is very well termed as acid catalyzed hydrolysis of a ketone to form a cyclic acetal.…

Q: 1. Design two syntheses of the compound below using the Grignard reagent and a carbonyl compound.…

A:

Q: (1) Mg, ether РСС он

A: Toluene  is an aromatic hydrocarbon. It is a colorless, water-insoluble liquid. Benzyl bromide is a…

Q: NH2

A: For this transformation,  SHAPIRO Reduction is used . Here the the concept of umpolung or the…

Q: Select the best reagents to effect the given transformation.

A: Answer : option B is the correct answer. When aldehyde react with NaBH4 in water it will leads to…

Q: Please help me solve this synthesis. It takes 5 steps

A: OKAY, I will give complete synthesis by using 5 steps.  You can see step by step solution. How to…

Q: Choose the correct product for this reaction.

A: Ketone under goes nucleophilic addition  reaction , from reagent CN- (cyanide nucleophile ) is…

Q: Ethane

A: We have to propose a synthesis from ethane to butan-2-one. The required synthesis is shown below

Q: Design a stepwise synthesis to convert cyclopentanone and 4-bromobutanal to hydroxyl aldehyde A.

A:

Q: Draw the expected product from the reaction here:

A:

Q: Based on the general procedure and reaction scheme, how much of every reagent would be needed to…

A: Given: 4-hydroxycoumarin = 1 mmol aromatic aldehyde = 1 mmol methylcarbamate = 1.5 mmol and p-TSA =…

Q: Indicate the reagent needed for the below reaction: н он

A:

Q: Propose an efficient synthesis process for this transformation. HO,

A: Williamson Ether Synthesis: Williamson ether synthesis is a type of coupling reaction for the…

Q: What are the steps and reagents used?

A: Applying concept of organic synthesis and reagent.

Q: Show how the benzaldehyde can be prepared from benzene:

A: Preparation of compound from reacting species with the help of various reagents is achieved.…

Q: 6 Show how to synthetize the following target: (a)

A: Organic reaction mechanisms.

Q: Show how to convert each starting material into benzylamine in good yield

A:

Q: Br. NH2

A: Benzene is an aromatic compound. It has a six membered cyclic planar structure with six delocalized…

Q: HO

A:

Q: a synthesis for the fellowing transformation. To

A: See synthesis below.

Q: This is the reaction I was referring to, I have no idea of what reagents can lead me to the…

A: In this reaction, the reagents are H2O and KMnO4.

Q: Explain why a Lewis acid is necessary in this aldol reaction. Include a structure formed by the…

A: Lewis  acid  Facilitate  the attacking of nucleophile  to the carbonyl  carbon

Q: Draw the two ethyl esters which could be used to make the mixed Claisen product shown below.

A: Clasien ester condensation :  The Claisen condensation is a carbon–carbon bond forming reaction that…

Q: NH2 NH2 CI

A: For this transformation , We have to use first a) Fe/Cl2   b) Acetylation

Q: Devise a synthetic strategy to complete the following transformation. HOʻ

A:

Q: How can this product be synthesized via a Michael reaction.

A: Addition of active CH group at α,β-unsaturated carbonyl, cyano, ester, nitro compounds in basic…

Q: Show a reaction with nucleophilic substitution.

A: Nucleophilic substitution reaction is the reaction where Nucleophile ( i.e electron reach atom or…

Q: Show how you could synthesize 3,5-dichlorophenol from phenol and any other reagent. он он CI

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

Q: Propose an efficient synthesis process for this transformation. HO HO

A: Given reaction,

Q: What is a multi-step synthesis for the following:

A: The final product can be prepared in the following steps:Step 1 : Preparation of alkene from alkyl…

Q: fill in the product. which crown ether would be best to use in the following reaction to help the…

A: To dissolve the starting material, 18-Crown-6 with a molecular formula of C12H24O6 will be the best.

Q: reagents

A: Friedel crafts alkylation reaction are mostly used in this question.

Q: draw the product

A:

Q: Give a reaction you could use to convert Benjamin to aniline

A: Organic reaction mechanisms conversation of benzene into aniline.

Q: Which reagents would you use to perform reaction B?a) PBr3.b) p-toluenesulfonyl chloride.c) SOCl2.d)…

A: The given reaction is shown below:

Q: Br

A: Organic reaction mechanisms.

Q: H

A: Applying concept of organic synthesis via wittig reaction and organometallic.

Q: DH

A:

Q: How would I use Gabriel synthesis here?

A: Gabriel synthesis:

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

A:

Q: Need help finding the order of Reagents  to form the product

A:

Q: 4. Give a short, efficient synthesis of the target compound from the indicated starting material and…

A: The required synthesis is as follows:

Q: Devise a synthetic strategy to complete the following transformation. HO

A: Here we have to synthesize the following componund by retrosynthesis analysis and then by forward…

Q: Explain Tautomerization with example?

A: Tautomerization

Q: OH

A:

Designing a Synthesis

Organic synthesis is a branch of chemical synthesis that involves the planned construction of organic compounds/molecules from smaller units that possess functional groups. Friedrich Wöhler was the first scientist who designed the synthesis of an organic compound, urea from inorganic starting materials silver cyanate with ammonium chloride via a simple, one-step synthesis.