Based on the image attached, explain the step-by-step mechanism reaction of reduction for methyl-2-hydroxybenzoate that formed 2-hydroxymethyl phenol as a product.

Q: Hello, can you describe the product formed as a result of the reaction between benzoic acid and…

A: The reaction between a carboxylic acid and an alcohol results in the formation of an ester and the…

Q: What is a mechanism for the formation of a hemiketal from the reaction of butanone with 2-butanol?

A: A hemiketal can be defined as a compound which results from the addition of alcohol to a ketone.…

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: Give the product of the following reaction.

A: Given,

Q: 5. Show a correct scheme (show all structures and reagents) that can be used to synthesize…

A: There are many steps involved in synthesising p-chlorophenol from benzene like electrophilic…

Q: Propose what you would have observed in this experiment (oxidation of borneol into a ketone) if you…

A: The answer is as follows:

Q: Use retrosynthetic analysis to show how hex-3-yne can be prepared from acetylene and any other…

A: Hex-3-yne can be synthesized from acetylene using suitable reagents. This can be shown using…

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: Acetal formation must be catalyzed by an acid. Explain why it cannot be catalyzed by CH3O-.

A: Since in the reaction, CH3O- can not replace the OH- group. This is because CH3O- is a better…

Q: Write down how to synthesize 2-phenyl-3-methyl-3-pentanol using all the reagents you want, along…

A: In this question, we have to find out the correct answer of given problem by the help of the…

Q: The haloform reaction is an efficient method for converting methyl ketones into aldehydes.

A: Haloform reaction : In those carbonyl compounds where keto-methyl group is present , that carbonyl…

Q: Show how the m-bromobenzonitrile can be synthesized from benzene:

A: Benzene is an aromatic compound. It consists of a six membered cyclic ring having alternate double…

Q: Show how the m-methylnitrobenzene can be synthesized from benzene :

A: Given reaction,         Synthesis of m-methylnitrobenzene from benzene

Q: What is the major product of bromination of p-methylbenzoic acid reactions?

A: p-methylbenzoic acid is an aromatic compound in which benzene ring is substituted with a carboxylic…

Q: What types of compounds give haloform reactions? show on examples

A:

Q: Explain and show step by step how did the product formed when pentanoic anhydride is treated with…

A:

Q: Write the mechanism of the aliphatic nucleophilic substitution reaction between n-butanol and Br- in…

A:

Q: Draw the structure of the meso diol and of its corresponding acetonide.

A: Structure of meso-hydrobenzoin is:

Q: Give the product of the following transformation:

A:

Q: Show the reaction mechanism for synthesis of Cyclopentane-1,2-diol from Cyclopentane-1,2-dione using…

A: LiAlH4 is used as reducing agent. It reduces ketone into secondary alcohol. It is an nucleophilic…

Q: Ilustrating with an equation show how oxirane can be converted to 1,2 -diphenoxyethane

A: The conversion from oxirane to 1,2, -diphenoxyethane is shown as,

Q: The reaction that occurs when the benzaldehyde you have is reacted in a basic environment is called…

A: We have to give mechanism of cannizaro reaction and benzoin condensation

Q: Draw in the missing structures A and B, and then choose what could function as reagent C to complete…

A: In this question, we have to draw the missing structure A,B and the reagent C.

Q: Write the complete mechanism for the hydroxide ion catalyze reaction of cyclohexanone and…

A: Hydroxide ion (OH-) act as a catalyst which can abstract the acidic alpha proton to form the enolate…

Q: Show structures (in blank boxes) for the reactants/products/reagents in the following reactions.

A: In given question, first reaction is reduction reaction and LiAlH4 acting as a reducing agent.…

Q: Please show in details how to prepare the target molecule? You must use benzene as one of your…

A: The given compound is asymmetrical ketone. Benzene can be converted to tert-butyl benzene via…

Q: What is the mechanism of the acid-catalyzed acetal formation of benzaldehyde in methanol?

A: In this reaction, first the carbonyl group of benzaldehyde will be protonated, which will increase…

Q: Show the complete and detailed reaction mechanism (oxidation reaction) of 3-bromobenzyl alcohol in…

A: 1 CeCl3  is catalyst  act as Lewis Acid attact on       oxygen lone pair.

Q: Show the chemical equation of N,N- Dimethyl aniline reacts with Diazotized Sulfanilic acid to form…

A: Reaction :        When Diazotised sulphanilic acid react with N,N-dimethylaniline, it is first…

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: 1. What is the chemical reaction involved i the synthesis of methyl salicylate? 2. Give also the…

A:

Q: Show how the 2-phenylpropene acid can be synthesized from benzene:

A: I consider the synthesis of 2-phenylpropene from benzene. Because a compound called 2-phenylpropene…

Q: Can you make the mechanism for the synthesis of diphenyl methanol from benzaldehyde?

A:

Q: Show how the m-xylene acid can be synthesized from benzene:

A: Given: Synthesis of m-xylene from benzene

Q: Show how the m-chlorobenzaldehyde can be synthesized from benzene :

A: Friedel- Crafts acylation and chlorination forms m-chlorobenzaldehyde from benzene.

Q: Show how the benzyl methyl ether can be synthesized from benzene:

A: To show the preparation of benzyl methyl ether from benzene:

Q: single reaction sequence: a certain ketone undergoes alkylation to give new ketone, when reacted…

A: Acetone reacts with t-BuOK gives enolate ion. This enolate ion reacts with propyl bromide gives…

Q: Draw the reaction mechanism of the elimination reaction of 2 bromobutane with a hydroxide ion acting…

A: Elimination reaction : An elimination reaction is a type of chemical reaction in which several atoms…

Q: Draw the detailed arrow pushing mechanism for the conversion of methyl benzoate to triphenylmethanol

A: To do : conversion of methyl benzoate to triphenylmethanol

Q: What product is formed as a result of nitration reaction of 2,5-dimethylbenzoic acid?

A: The structure of 2,5-dimethylbenzoic acid is as follows:

Q: What species other than an acid can be used to increase the rate of the transesterification reaction…

A:

Q: Show a mechanism for the conversion of any aldehyde or ketone and any alcohol (as solvent) to the…

A: When an aldehyde or a ketone is treated with an alcohol in present of HCl or any other strong acid…

Q: Show the reaction mechanism when phenol is reaction with a solution of Br2 and glacial acetic acid.

A: Phenol reacts with bromine and undergoes bromination reaction to produce p-bromophenol as major…

Q: Kindly show the mechanism when you synthesize 2-hydroxypropanoic acid from ethanol

A: We have to show mechanism

Q: Show how the m-bromoiodobenzene can be synthesized from benzene:

A: In the substitution of benzene, EDG are ortho-para directing groups whereas EWGs are meta directing…

Q: Show how the benzyl alcohol can be synthesized from benzene:

A: Benzyl alcohol is represented as a -CH2OH group attached to the benzene ring.

Q: Based on the image attached, i) explain details on the nitration reaction of methyl salicylate.…

A: Nitration :  Nitration is the substitution of nitro(NO2) group of one of the hydrogen on benzene…

Q: Draw the structure of the major product that would be obtained from the dehydration of…

A:

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.