Give the reagents necessary for the synthesis above and please show the detailed step-by-step mechanism.

Q: provide a possible synthesis for the following reaction

A:

Q: Give the major organic product for the following reaction

A: We have to predict the major product for the following reaction :

Q: Provide the missing reagents in the following multi-step synthesis.

A: The organic reaction is given with missing reagents and it is required to complete the reaction by…

Q: Provide the mechanism for the 1st reaction in this synthesis: КОН

A: We have to draw the mechanism of given reaction

Q: Propose

A: When alcohol is heated then water molecule gets eliminate and we get alkene.

Q: and give the major product formed

A: Alkynes undergo addition reaction with electrophiles like halogens. Halogens are attached with the…

Q: Propose a reasonable synthetic route for the following conversion. Show all isolated intermediates.

A: Answer is given in below image

Q: Select the appropriate sequence of reactions to accomplish the following synthesis.

A: The starting material ethyl methyl ketone contains active methylene group and so undergoes…

Q: provide synthesis for this reaction including all reagents and mechanisms with steps ↑

A: This can be done like this

Q: Propose a reasonable mechanism to explain the following Reactions.

A: Mechanism of above reaction is given below.

Q: Provide the major organic product of the following reactions. Show the complete arrow pushing…

A:

Q: In the following reaction, propose a mechanism that explains its formation:

A:

Q: Show the step by step synthesis of the following compound.

A: First add Cl on benzene via Electrophilic substitution recation  Then reaction with NaOH which gives…

Q: Provide detailed reagents and conditions, in the correct sequence, required to form products B, C…

A: When compound A is treated with NaOMe then corresponding anion is formed which reacts with CH3CH2CHO…

Q: Give the major cyclic product for the following reaction

A:

Q: major products obtained from the following sequence of reactions are:

A: Ans. Option C will be correct.  This is Hoffman Exhaustive Methylation reaction :  The procedure of…

Q: Propose a mechanism for the following reaction and develop it.

A: Given Reaction is known as Dienone phenol rearrangement reaction .

Q: Propose a mechanism for each of the following rearrangement reactions:

A: Hello. Since your question has multiple parts, we will solve the first question for you. If you want…

Q: heel HO он NaOH (a)

A:

Q: illustrate detailed mechanisms to complete the reaction

A: Alcohol reacts with HBr gives a rearranged product. Intermediate is carbocation, hence carbocation…

Q: The following synthesis will no produce the product shown - explain what will happen instead

A: Concepts to be used: Lewis acid react with Lewis base preferably in friedel craft reaction.…

Q: What series of synthetic steps could be used to carry out the transformation shown below?

A: We have to carry out the given transformation.

Q: Give the major product for the following reaction

A:

Q: Select the best set of reagents for carrying out the following synthesis

A:

Q: Come up with a reasonable mechanism for the following reaction

A: In this question we want to draw reasonable mechanism for this reaction.  This reaction is Aldol…

Q: Provide the major monobromination product for each of the following reactions:

A: Note : As per our company guidelines we are supposed to answer only first 3 sub-parts. Kindly repost…

Q: Provide the major organic products for the following reactions.

A: We have given the organic reaction we have to provide product of the reactions.

Q: Provide the major product for the following reaction?

A:

Q: Synthesize From

A: The acidic proton in the ketone substrate can be abstracted by the base in order to generate…

Q: Give a mechanism for the following reaction.

A: We have to predict the mechanism.

Q: Provide a synthesis of the following target from the given starting material. from benzene

A:

Q: a) ホ→ OMe b)

A: Number of functional group is associated with organic compounds which impart specific chemical and…

Q: provide a synthesis with the starting being Benzene

A: Solution-  synthesis of the following compound with the starting being Benzene is drawn below;

Q: provide a mechanism for this

A: Given reaction is a example of E2 reaction .This is a one step reaction in which Hydrogen is removed…

Q: Provide a step-by-step mechanism for the following reaction. он

A: order of Stability of carbocation : 3° > 2° > 1° In this mechanism, the first step is the…

Q: Synthesize the following ether from any two alcohols. YOU MUST SHOW the complete retrosynthetic…

A: synthesis of ether from alkylhalide and alkoxide ion is aceed williamson etherification   To do…

Q: What is the major organic product obtained from the following sequence of reactions?

A: Major product in this reaction:

Q: но.

A: A detail solution is given below -

Q: O Complete the following reaction and provide a detailed, step-by-step mechanism for the process.…

A:

Q: Give the major organic product for each step of the following reaction

A:

Q: What synthesis would result in the product shown below as the major product?

A: For the synthesis of given major product, we will carry out the William-ether synthesis.

Q: Give detailed mechanism of following reactions?

A: First step is conversion of ethyl 3-oxobutanoate (ester) to 3-oxobutanoic acid (carboxylic acid)…

Q: provide a synthesis of the target compound shown from the starting material that is provided

A: The synthesis of the target compound shown from the starting material that is provided is given…

Q: please help with this question. thank you. Propose a mechanism for this transformation

A: We have given the organic reaction we have to find the major product of reaction.

Q: Please complete the reactions given below.

A: Given reactions: g)                               h)                                i)…

Reactions of Ethers

Ethers (R-O-R’) are compounds formed by replacing hydrogen atoms of an alcohol (R-OH compound) or a phenol (C6H5OH) by an aryl/ acyl group (functional group after removing single hydrogen from an aromatic ring). In this section, reaction, preparation and behavior of ethers are discussed in the context of organic chemistry.

Epoxides

Epoxides are a special class of cyclic ethers which are an important functional group in organic chemistry and generate reactive centers due to their unusual high reactivity. Due to their high reactivity, epoxides are considered to be toxic and mutagenic.

Williamson Ether Synthesis

An organic reaction in which an organohalide and a deprotonated alcohol forms ether is known as Williamson ether synthesis. Alexander Williamson developed the Williamson ether synthesis in 1850. The formation of ether in this synthesis is an SN2 reaction.