OH

Q: Provide the reagents required.

A: Answer of the question given below,

Q: H₂C OH OH H+ CH3 Esters can be synthesized by an acid-catalyzed nucleophilic acyl substitution…

A: Here a step of mechanism of Fischer esterification reaction is given , we have to give arrows in…

Q: с) OH H. d) OH

A: (c) When Aldehyde treated with mild reducing agent like - sodium boro hydride, NaBH4, or metallic…

Q: 6. Provide the reagents or the product for the following reactions. スロダ b. HO C. PBr,

A: Alkyl halide reacts with alkoxide ion to form ether Carboxylic acid react with alkylhalide in the…

Q: CHCH3 1. Hg(OAc)2, H20 2. NaBH4 CH3

A: When alkene proceeds through mercuration demercuration process, then OH group attached with least…

Q: Propose a series of reactions that would convert the provided starting material into the given…

A: The question is based on the concept of organic synthesis. We need to synthesize the product using…

Q: Indicate the major organic product that would be formed under the conditions below: 1. ВН3 THF 2.…

A:

Q: What is the major organic product obtained from the following reaction?

A: Find out the major product.

Q: Draw the major organic product for the reaction: Br NaCI H20

A: Given,

Q: Which reagent is required for this reaction? H. PPH3 PPH3 PPH3 PPH3

A: Aldehyde or ketone reacts with the triphenylphosphonium ylide to form an akene, known as the Witting…

Q: H₂C H₂C ممل CH3 CH3 Aldehydes and ketones react reversibly with two equivalents of alcohol in the…

A: The objective of the question is to predict the suitable mechanism for the given reaction.Ketal…

Q: Give the product of the reaction.

A: The alkyl nitrile gives the hydrolysis reaction in the presence of an acid or base catalyst to form…

Q: For the following reactions, draw the MAJOR product(s). 1) Hg(OAc)2, H2O 2) NaBH4

A:

Q: What would be the Michael donor and acceptor?

A: Given that, a reaction scheme is shown below We have to identify the reactants A and B. Also, we…

Q: What is the balanced chemical equation for the aromatic bromination of Acetanilide using green…

A:

Q: 4. Aldehydes and ketones can be "protected" as acetals and ketals. Complete the following outlined…

A: Aldehydes and ketones are protected as acetals and ketals when treated with alcohols in the presence…

Q: H,C CO,H c3D c=C CH,CH;CH; H

A:

Q: Provide the appropriate reagents or product in the following examples.

A: Given ; reactant

Q: Provide synthetic routes for the preparation of the starting materials of azo dye Alizarine Yellow R…

A: Given are organic synthesis reactions.The given compounds are starting compounds of atoms dye…

Q: H2NNH2 CH3 H* H3C `CH3 H3C IZ

A: We have find out mechanism for 3,5 dimethyl pyrazole

Q: What is the source of the nucleophilic attack? How does the oxygen get protonated? What causes the…

A: Here nucleophilic attack , protonation and elimination occur in the given reaction.

Q: ÇI OH Но CI

A:

Q: ОН + …… ОН ОН

A: The question is based on the concept of organic synthesis.We need to synthesize the product using…

Q: 0 е НО.

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: НО, H3CH₂CO OH OH

A:

Q: What reagent/reagents is/are necessary to transform the starting molecule into the desired product?…

A: In this process, benzene sulfonic acid is reacted with aqueous sodium hydroxide. The resulting salt…

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.