Show how to bring about the following conversion  using a Wittig reaction.

Q: Propose a two-step synthetic strategy for the synthesis of 2-methylhexane from 5-methyl-2- hexanol.

A: it’s shown below:

Q: Write the reagents to carry out the following reactions:

A: To solve this problem we have to give the reagents to complete the reactions .

Q: ) Propose a reasonable synthesis for the formation of nonane from CH3CH2CH2I and  any other…

A: The question is based on the concept of organic reactions. we have to convert the reactants provided…

Q: What starting materials or reagents are best used to carry out the following reaction?

A: This transformation can be achieved by Friedel-Crafts alkylation. But, Friedel-Crafts alkyaltion…

Q: Identify the best reagents to complete the following reaction.

A: Aldehyde functional group is -CHO , ketone functional group is RCOR  Aldehyde and ketone both…

Q: Propose a reaction mechanism for the following transformation:

A: Answer is explained below.

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: Show two methods to synthesize each alkene: a one-step method using a Wittig reagent, and a two-step…

A:

Q: Propose a synthetic pathway to generate the molecule below. You may use benzene, alcohol, and alkyl…

A: This molecule can be generated by several step using malonaldehyde as a starting material.  There…

Q: Show the electron-flow mechanism of the synthetic schemes (Butyl Acetate) of the picture below. This…

A: Here we have to give the electron flow mechanism of above synthesis of butyl acetate-

Q: Show how to convert ethylene to 1,2-Ethanediol compound.

A: The conversion of Ethylene to 1,2-Ethanediol is as shown below:

Q: Propose a synthesis of 1 from 2 using reagents with no more than 3 carbons and any inorganic…

A: The starting material and the final compound given is,

Q: Make p-nitro phenol using suitable reagents, starting from benzene.

A: Benzene reacts with Cl2 in presence of AlCl3 to produced chlorobenzene, when chlorobenzene treated…

Q: What is the missing product or reagent needed to complete these reactions?

A: Nucleophilic substitution biomolecular reaction (SN2): The bimolecular nucleophilic substitution…

Q: Show how you would accomplish the following synthetic conversions efficiently and in good yield. You…

A:

Q: он 1. Pd'Ln, EtgN, MECN Me HO" 2. NABH4, MEOH 3. çI , ElgN, CH,Cl, Me

A: Step 1 : Heck coupling followed by isomerization. Keto to alcohol using NaBH4. O-acetylation of…

Q: Give the product of the following transformation:

A:

Q: Propose a stepwise mechanism that accounts for the transformations below.

A: The reactions involving organic compounds are called organic reactions.  Each organic reaction is…

Q: ...Br t-BUOH

A:

Q: write reagents of this reaction

A:

Q: Show two different methods to carry out the following transformation: a one-step method using a…

A: Concept introduction: The Wittig reaction accomplishes under the influence of "triphenylphosphonium…

Q: Write a reaction showing how this compound is prepared.

A:

Q: How to get the molecule given below by getting out of bromobenzene and using the reagents you want?…

A: The targeted Molecule can be synthesized by Bromobenzene. When Bromo benzene treated with Bromine in…

Q: .  identify the structure of A and B in the following synthetic scheme: Write out complete reactions…

A: By observing the nature of the reagents used,  we can expect ketone and imine as products…

Q: OH CH3 OH CH3 CH3 CH3 OH CH3 OCH3

A: Organic reaction mechanisms.

Q: Show reagents to bring about the following conversions

A: A reagent is defined as the substance or compound that is added to the system so that a chemical…

Q: Choose the best reagent to complete this reaction. Assume an acidic work up. NH2 NH2

A:

Q: Provide the reagents necessary to complete the following reactions. More than one step may be…

A: In this question, we have to synthesized the product from given reactant by using necessary…

Q: Complete the following malonic (di)ester synthesis by showing all reagents and reaction conditions…

A: The given reaction is,

Q: Identify the reagents that you would use to perform the following reaction:

A:

Q: Choose the best reagents to complete the reaction shown below.

A:

Q: Draw a structural formula for the product formed by treating butanal with each reagent. (a)…

A: Since the question you have posted contains multiple subparts, we can solve only first three…

Q: Propose a synthetic route for the following conversion:

A: 1. Alochols when they treated with acid it gives alkene by elimination of water  2. Alkenes are…

Q: Propose an arrow-pushing mechanism for the following transformation. НО H30+

A: The above transformation is associated with the carbocation. In this transformation hydroxyl group…

Q: 2) Show reagents that could be used for the following transformation:

A: Explanation to the correct answer is given below.

Q: When CO2 is bubbled through a solution of benzyl magnesium bromide, and the mixture is then…

A: Grignard reagent react with carbondioxide carboxylic acid formed.

Q: Which reagent would best accomplish the following transformation?

A: CH3CH2CH2CH2OH ---------------> CH3 CH2CH2CHO The best reagent used to oxidize 1-Butanol to…

Q: Starting from cyclohexanol, show how to prepare:

A: Racemic mixture: It is a mixture of two enantiomers which are in isomeric forms.

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: Make an electron-flow-mechanism for this synthetic scheme. This involves predicting major and…

A: By electrophilic substitution reaction benzene is converted to benzene sulphonic acid

Q: Show how you would synthesize octan-2-one from each compound. You may use any necessary reagents…

A: SOLUTION: Step 1: Heptanoic acid reacts with LiOH to form lithium carboxylate. This is followed by…

Q: Write the mechanisms for the following reactions bellow, justifying each substitution position.

A: The first part is electrophilic chlorination. The chlorination occurs ortho and para to the acetyl…

Q: Provide the reagents necessary to complete the following reactions.

A: Organic Reagents are an important part of the synthesis that helps in converting the reactants into…

Q: An equimolar amount of the three compounds below are mixed and treated with base followed by an…

A: this behave as nucleophile ans when base react with this compound base deprotonate acid hydrogen…

Q: For each of the following, provide the product or reagent as necessary H20 NaBH4 + Hg(OAc)2 ELOH а)…

A:

Q: how you would carry out the following chemical conversion

A: The carry out the above conversion i.e ester to acyl chloride, following steps will be required. 1)…

Q: Propose a sequence of steps to perform the following transformation

A: Given,

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.