Write the explicit formulas of A, B, C and D in the synthesis below.

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: complete the reactions below by writing the major product

A: Given,

Q: Он 2-pentanol 3-pentanone

A: Alcohol when heated in the presence of acid give alkene which on addition with water give alcohol.…

Q: Complete each of the following statements below using the figure below. NaOH a. In the above…

A: Nucleophile is negatively charged or neutral species. Electrophile is positively charged or neutral…

Q: (1) Mg, ether РСС он

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

Q: Give a Grignard reaction where the following reagent will participate.

A: Grignard reagent is prepared by halocompounds reaction with magnesium. In these reactions, the bond…

Q: Give the reagents necessary for the synthesis above and please show the detailed step-by-step…

A: The reactant is Ethyl acetoacetate. The reactant contains the methylene protons which are highly…

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: Outline the synthetic steps necessary to carry out the conversion below. You may use any organic or…

A: We have to carry out the required conversion.

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

A: Answer is given in below image

Q: Write a synthesis for the following from

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

Q: O,N. Br O2N

A:

Q: The best reagents for accomplishing the above transformation are:

A: We have to tell which option is correct from given choices of options

Q: Select reagents from the table to show how you would carry out this synthesis.

A: The given substrate is 1-pentene. The given reaction is the conversion of 1-pentene to pentanal. The…

Q: 2. Provide a synthetic approach for the following reactions. Make sure to do the retrosynthetic…

A: the given target molecule is 3° alcohol. This alcohol is prepared from a ketone and grignard…

Q: 3. Show how you could efficiently synthesize the products in (a) and (b) from the assigned starting…

A: Both reaction done in handwritten solution

Q: Suggest the starting reagent in the following reaction:

A:

Q: Provide the reagents needed to complete the following synthesis.

A: Given : reactants and products

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: c) Outline a synthesis for compound G shown below starting with a 2- hydroxybenzylketone.

A:

Q: Please give the appropriate reagents FOR 1, 2 AND 3 to complete the following synthesis. 1 2 3.

A: given reaction is  by using Corey-house synthesis reaction we can get the product

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

A:

Q: For each of the following transformations, propose a realistic synthesis:

A:

Q: O.

A: The scheme represents the conversion of toluene to methyl benzoate.

Q: Y.. HN HN MEOH, H2SO4 NaOH HO. Work through the above synthesis and draw the structure of compound…

A:

Q: NH2 NH2 CI

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

Q: Write the following synthesis with the mechanism using the appropriate reagents. но

A: We have given that Malonic Ester  to carboxylic acid

Q: Give the reagent(s) that would accomplish the following reaction:

A: Since you have asked two questions, we will solve the first question for you. If you want any…

Q: Below are several common solvents in organic chemistry. Select those that would not be compatible…

A: Given : structure of molecules Grignard does not react with ether, alakne, benzene

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: НО.

A:

Q: Give the major organic product(s) each of the following reactions

A: Since you have asked a question with multiple sub-parts, we will solve the first three sub-parts for…

Q: 2. Propose a reasonable synthesis of compound 2 from compound 1. Use no more than 4 steps. Он он он…

A: "Ardnt-Eistert Homologation" is mainly used for the conversion of a carboxylic acid to larger…

Q: Propose an efficient synthesis for each of the following transformations: .CI

A:

Q: Provide the reagents and mechanism for each step of the synthesis.

A:

Q: If we wanted to carry out the synthesis indicated below What would be the starting material…

A: Alkyl halide reacts with magnesium to form grignard reagent, which furthur reacts with CO2 to form…

Q: Which synthesis of a grignard reagent would fail to occur as written

A: Grignard reagent can be prepared from alkyl or aryl or vinyl halides and Mg metal .  During the…

Q: Give the major organic product for each of the reactions

A: To solve this problem we have to give the major products formed by the given reaction .

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 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: directions if you wish.) 3. Provide a complete curved-arrow mechanism for the following…

A: In Gabriel synthesis, potassium phthalimide gives a nucleophilic substitution reaction with a…

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: Perform a retrosynthetic analysis by working backwards two steps in the synthesis below. Identify…

A: Given is retrosynthetic analysis

Q: The compound below can be prepared with an alkyl iodide and a suitable nucleophile. Identify the…

A: The given structure of the compound appears as follows: The structural formula of the above…

Q: Starting with benzene and other necessary reagents, design a synthesis for the following compound.

A: This can be done by Acylation and then chlorination .

Q: Make a suggestion of the reagents required to produce the following:

A: The functional groups of a molecule are a key component that plays a significant role in providing…

Q: Write an efficient synthesis for the following transformation

A: As per guidelines if multipart questions posted , first question is allowed to answer, please repost…

Q: propose a detailed, stepwise synthesis of methyl yellow with benzene and chloromethane as your only…

A: Here we are required to show stepwise synthesis of methyl yellow with benzene and chloromethane

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.