How will you Synthesize benzyl the following morecule from bromide ?

Q: но но, HO,

A: Conversion of one compound to another takes place with the help of various reagents.

Q: Please synthesize each of the compounds shown below from benzene

A: Benzene on treatment with chlorine in the presence of anhydrous AlCl3 produces chlorobenzene.…

Q: What ylide and carbonyl compound would you need to synthesize the alkene shown?

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

Q: from OH

A:

Q: N. d)

A: The question is based on the concept of organic synthesis. we have to identify the carbonyl…

Q: How would you synthesize the following compound from benzene?

A:

Q: H.

A: Based on the following transformation, provide or propose an efficient synthesis

Q: How would you carry out the following synthesis of cyclohexane cyclohexanol cyclohexane

A: Note:Hey there! Thank you for posting the question. Since the question is not complete, the…

Q: Show how you would synthesize the following from benzene and other pertinent inorganic/organic…

A:

Q: . Show how the enamine below can be synthesized. Then draw the resonance structure(s) for the…

A:

Q: How would you synthesize the following substances from benzene, use rSNA in as many steps as…

A:

Q: Propose products (if any) and mechanisms for the following AlCl3@catalyzed reaction of methyl…

A:

Q: Show how you would carry out the following synthesis. ? OH

A: Given substrate is alcohol and desired product is alkene  Dehydration of alcohol gives an alkene…

Q: Show how you might synthesize the following compound  from a haloalkane and a nucleophile.

A: SN2 Reaction: It is a nucleophilic substitution reaction in which the rate determining step depends…

Q: How would you carry out the following reaction?

A: We have to tell how given reaction can be carried out

Q: Identify all carbonyl compounds that can undergo nucleophilic addition reactions from the following…

A: Carbonyl groups can undergo nucleophilic addition reactions, The extent of reactivity of carbonyl…

Q: How would you carry out the following transformation? ? ? ÓH

A:

Q: How would you carry out the following reactions

A: Please note- As per our company guidelines we are supposed to answer only one question. Kindly…

Q: g) h) N

A:

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: NH2 (Benzyl amine) (a) H.

A:

Q: Predict the major product(s) for the following reaction: D. pyridine

A: The given compound is di-phenyl amine. Here we have to determine the product form when di-phenyl…

Q: Starting from 1-bromoethane, synthesize ethanenitrile

A: as per guidelines if multiple questions first part is allowed to answer, please repost rest of the…

Q: Bombykol is the sex pheromone of the silk moth.

A: Suzuki Coupling : It is a cross-coupling reaction between organic halide and organocarbon compounds…

Q: Propose a synthesis for the following compound

A: To solve this problem we have to do it in multiple steps to get the desired product .

Q: Propose products (if any) and mechanisms for the following AlCl3-catalyzed reactions:…

A: The details solution for this is provided below in step II.

Q: B) Provide the minimum reagents required for the following syntheses below. Me. Me. OMe HO,

A: In the given reaction 1, ester undergoes hydrolysis to produce carboxylic acid in the presence of…

Q: How would you carry out the following synthesis? CCH3 SO3H

A:

Q: Propose a synthesis for the following compound.

A: The question is based on the concept of organic reactions.   We have to convert the reactant into…

Q: What would be the product of the following reaction? Suggest a mechanism. H+

A: The reaction of a reactant thio-ester undergo acid hydrolysis is as follows, firstly lone pair of…

Q: Synthesize the following molecule using any reagents you desire. Ph HO,

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

Q: How would you synthesize the following ether?

A:

Q: Show how you would use direct alkylation to synthesize the following compounds.(a)…

A: Benzyl trimethyl ammonium iodide can be prepared by the direct alkylation reaction of benzyl amine…

Q: Please synthesize each of the compounds shown below from benzene.

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

Q: How would you carry out the following synthesis?

A: a. Friedel-Craft acylation followed by bromination then Grignard reagent preparation and then…

Q: Show how you would use direct alkylation to synthesize the following compounds benzylamine

A: SOLUTION: Step 1: Reaction of benzyl chloride with excess of ammonia results in the formation of…

Q: Show how you would synthesize the following derivatives from appropriate carbonyl compounds

A: The given compounds are imine derivatives, which can be prepared from corresponding carbonyl in…

Q: Show how you would synthesize the following derivatives from appropriate carbonyl compounds. (b) (c)

A: The carbonyl compounds on treatment with amines forms Schiffs bases.

Q: From butylbenzene synthesize the following compound

A:

Q: Along with aniline, which reagent is needed to synthesize the following dye: HO, ‚N. LOCH OH LOH E…

A: For the dye formation, we use the  NaNO2/HCl which form the diazonium salt and then another reactant…

Q: Propose a synthesis of the following product beginning from benzene. HN.

A:

Diol

In chemistry there are so many chemical compounds that have a hydroxyl group but a chemical compound having two hydroxyl groups (-OH) is termed as a diol. It also implies the presence of two alcohols whereas polyols contain two or more than two hydroxyl groups (-OH). Glycol or 1,2-diol is an aliphatic diol that has two alcohol groups on adjacent carbon atoms. In industries, the most commonly used diol is ethylene glycol.