How would you perform the following syntheses? You may use any specialized organic reagents, inorganic reagents and solvents that you need. Need to utilize the given starting materials.

Q: Show reagents and experimental conditions you might use to convert each starting material into the…

A: But-2-en-1,4-diol undergoes hydrogenation with transition metal as catalyst to give 1,4-butandiol.

Q: Starting from Benzene as the only organic reagent you have and use any other inorganic reagents to…

A: The reaction of benzene to 2-Phenylethanamine

Q: a) Acetoacetic ester can be prepared from Claisen self-condensation reaction of ethyl acetate. You…

A:

Q: Show how to synthesize the following compound using any necessary reagents. All carbon atoms come…

A: GIVEN:-

Q: Provide all reagents, material, and solvents needed to complete the following transformations. Any…

A: Hey, since there are multiple questions posted, we will answer first question. If you want any…

Q: From the compound below, illustrate how will it be synthesized starting with benzene? Provide the…

A:

Q: Propose a synthesis to make 2-Butanone using Ethanol as the only starting material with carbon…

A:

Q: Show how to synthesize the following compound using any necessary reagents. All carbon atoms come…

A: GIVEN:-

Q: 3) Provide a synthesis of the following compounds using the given starting materials as your only…

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

Q: HO, ОН

A:

Q: How can you prepare the following compound with benzene as one of the starting materials?

A: On treating the benzene with Cl2 in the presence of AlCl3, chlorobenzene is formed.

Q: SYNTHESIS! Devise a multistep synthesis of the target molecules from the given starting compound.…

A: Bromobenzene is converted into phenylmagnesiumbromide (grignard reagent) further it is treated…

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

A: Heptanal is a compound that has seven carbon atoms and an aldehyde functional group is present. The…

Q: Show reagents and experimental conditions you might use to convert propyne into each product. (Some…

A: Given conversion,

Q: What reagent would you use to accomplish the following reactions?

A: Hello. Since the question contains multiple subparts, the first three subparts are solved. In case…

Q: Design a synthesis for each of the following compounds, usingany inorganic reagent of your choice…

A: a. Octanal = The synthesis of the given compound is,

Q: 3) Provide a synthesis of the following compounds using the given starting materials as your only…

A: First convert the given alkyne as an electrophile (as an alkyl halide) by reducing alkyne to alkene…

Q: Show how to convert cyclopentanone to these compounds. In addition to cyclopentanone, use any other…

A: Cyclopentanone undergoes reduction using hydrogen in palladium, or lithium aluminium hydride, or…

Q: 1. Using any reagents necessary, propose an efficient synthesis for each of the following…

A:

Q: By means of series of equations, show how each of the following synthesis can be carried out. You…

A:

Q: What

A: We will write the reaction mechanism

Q: The following diol is prepared from propanal (CH3CH2CHO) and 3-bromopropanol. Which derivatives will…

A: Grignard  reaction  - is the reaction  that uses on organometallic compound to create carbon- carbon…

Q: Show reagents and experimental conditions you might use to convert each starting material into the…

A: Interpretation: The reagents and experimental conditions required to convert 2-hexyne to given…

Q: Starting with phthalamide (below), provide a step-by-step synthesis of the amine shown below. You…

A: Formation of primary amine by Gabriel pthalamide synthesis. PCC oxidize alcohol to ketone. And…

Q: (c) Starting with benzene and using any other necessary reactants/reagents, show all synthetic steps…

A: In this question, we will give the following transformation starting from benzene and using all the…

Q: : Starting from Benzene as the only organic reagent you have and use any other inorganic reagents to…

A: First step for synthesizing this compound is Friedel-Craft Alkylation reaction of Benzene: 1.

Q: Starting with cyclohexanone and ethanol as the only organic reagents, use any inorganic reagents to…

A:

Q: Show reagents and experimental conditions you might use to convert propyne into each product. (Some…

A:

Q: How would you accomplish the following synthesis? You may use any specialized organic reagents,…

A: In the above reaction, we can see that there is a net addition of OH and C≡CH. And the addition is…

Q: Propose a synthesis of the following molecule using benzaldehyde as your only source of carbon.…

A: GIVEN:-

Q: Draw the structure of the two ketones which may be used to make the tertiary alcohol shown below by…

A:

Q: Starting from benzene as the only organic reagent you have and use any other inorganic reagents to…

A:

Q: Synthesise the target molecules drawn below using precursor chemicals within the following…

A: Aspirin can be synthesized from Salicylic acid on acetylation with acetic anhydride . Aspirin has…

Q: OH OH

A: Desired product can be achieved in the several steps including oxidati e cleavage od double bond

Q: Starting with cyclohexanone, show how to prepare these compounds. In addition to the given starting…

A: Cyclohexanone is an organic compound with ketone as the functional group. To prepare…

Q: Propose a synthesis of the following compound starting from benzene, and 1, 2, or 3 carbon alcohols…

A: Here we have to synthesize the following given compounds from starting material benzene and 1,2 or 3…

Q: In order to synthesize the following ethers using the Willamson synthesis method, what would you…

A: Ethers are prepared by using Williamson synthesis. Williamson synthesis is an SN2 reaction between…

Q: Show how the following compounds could be prepared from the given starting materials. You can use…

A: Since you have posted question with multiple sub-parts, we are entitled to answer the first 3 only.

Q: Use RSA, including disconnections, synthons and synthetic equivalents to show how to prepare the…

A: Detail synthetic scheme is shown below

Q: Starting from acetylene, propose a synthesis for the following compound. Use any other organic or…

A: The structure of acetylene is: It is a 2 carbon alkyne hydrocarbon.

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

A: Answer: Octan-2-ol is secondary alcohol, which –OH group present at secondary carbon (C2) of octane…

Q: Starting from benzene, show how to prepare the following compound. show all the reagents and draw…

A:

Q: How would you perform the following multi-step syntheses using propiophenone, piperidine and any…

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.