3. Please provide a complete step-wise synthesis of the target molecule showing all steps, reagents and intermediates. `NH2

Q: Br, A Provide an acceptable synthesis for the following 1 SAI 2) Gon all

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Q: Complete the following schemes by assigning the missing products or reagents. KOC(CH3)3 Br2 CH3I E…

A: Given reaction is:

Q: Ph Ph ОН BF3 Benzene

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Q: How is this reaction is carry out ? Show all the steps please arrows and all the movement of…

A: The conversion of a primary alcohol to carboxylic acid via aldehyde is the oxidation reaction.

Q: 2) Write a detailed mechanism for the following reaction: он H30* OH

A: we have given that acid catalyzed epoxide opening to give diols.  the details mechanism of reaction…

Q: The following synthesis requires more than one step. Specify the reagents you would use to carry it…

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Q: Fill in the appropriate reagent or starting material in each of the attached reaction.

A: The nucleophilic substitution reaction is an organic reaction in which the nucleophile attaches to…

Q: In the boxes below, enter the LETTER for the reagents needed in each step to complete the following…

A: Here we are required to find the reagent needed for the following conversion of reactant to product…

Q: Give detailed answer- Provide example of compound that fulfil each criteria below. Explain why-…

A: Dear student since it is a multiple subparts questions,  according to bartleby guidlines here i am…

Q: Give a multistep synthesis of the molecule below. All carbons in the final molecule must come from…

A: Addition of H2O to alkyne:

Q: 3. Provide a synthesis of the following molecule starting from benzene. Br NO2

A: - In order to get the desire product one should follow the following steps :-  Step 1 :-  FC…

Q: 2. Write the synthetic procedure for the target compound with your own idea. (At least more than 5…

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Q: 1. Complete the following reactions, with the major organic product. a. CH3-CH=CH2 + Br2, b. + Br2

A: The major products are

Q: Question is attached as an image

A: The given compound reacts with THF gives disubstituted borane compound. The disubstituted borane…

Q: please provide synthesis starting from benzene, use the least amount of steps possible. OCH3 N. CB 3

A: Benzene can be converted to the given compound as follows: Firstly, benzene is treated with Lewis…

Q: 2. (from Review) Propose a sequence of reagents for the following transformation [Chapter 11,…

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Q: Show how HC≡CH, CH3CH2Br, and (CH3)2CHCH2CH2Br can be used to prepare CH3CH2C≡CCH2CH2CH(CH3)2. Show…

A: SN2 reaction:  The alcohols is reaction with acids like hydrochloric acid or hydrobromic acid, the…

Q: 4. Provide a multi-step synthesis of the diol drawn below (racemic, but free from other…

A: Multi-step organic synthesis:

Q: OCH3 NH, OCH3

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Q: Show the relationship between E2 Reactions and Alkyne Synthesis ?

A: Interpretation: The relationship between E2 reactions and alkyne synthesis is to be shown.

Q: 3-chloro-6,7-dimethyloct-1-ene and (E)-1-chloro-5,6-dimethylhept-2-ene are primary and secondary…

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Q: Draw the starting alkyl chloride that would produce this alkyne under these conditions. 3D 3D…

A: Dialkyl halides undergo an elimination reaction in the presence of a strong base such as NaNH2 to…

Q: Suggest a synthesis for the molecule shown below. Only starting materials containing six (6) carbons…

A: We can get the final product by taking terminal alkyne as a starting material and we can expect…

Q: 5. Retrosynthesis. Suggest how the molecules mentioned below can be synthesized (give the reagents…

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Q: Suggest a synthesis for the molecule shown below. Only starting materials containing six (6) carbons…

A: The key reactions involved in the synthesis of given target material are: 1) Friedel-Crafts…

Q: 2) Write a detailed mechanism for the following reaction: H2S04 CH;CH;C=CH + H,O CH;CH¿CCH3

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Q: The following synthesis requires more than one step. Specify the reagents you would use to carry it…

A: To Solve this problem we have to complete the given reaction using the given reagents .

Q: CI Which reagents lead to this transformation? O 1. C2, AICIl3 2. CH3CH2CI, AICI3 O 1. CH3COCI,…

A: The details solution for this is provided below in attach image.

Q: the given compounds. Write your answers on the space/field provided. Separate the reagents with a…

A: The answer is as follows:

Q: 2. (for multiple choice questions circle the correct answer(s)). (a) Provide the necessary reactants…

A: Williamson ether synthesis — alkyl halide (R—X) react with alcohol (R'—OH) gives an ether ( R—O—R')

Q: 2) After each reaction arrow, draw the structure of the expected major organic product(s). (A) 1)…

A: Applying concept of wittig reaction

Q: Show the reagents and experimental conditions necessary to bring conversion in good yield.

A: The reagents and experimental condition has to be given for given convertion.

Q: 3) write a detailed mechanism of: HO -OH CH3ČCI AICL3 CCH3

A: The reaction of phenol with acetyl chloride in the presence of anhydrous AlCl3 to form…

Q: 3. For the following synthetic schemes, please draw the product(s) to the right of the arrow. 1.…

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Q: CH2 H3C OSO2CF3 С. CF3CO2H O-H `CH3 CF3- CF3SO3 + `CH3 a nonnucleophilic polar solvent O-H

A: Mechanism for the following reaction is

Q: For the transformation below, give the structure of all possible starting alkyl bromides. H CH3…

A: Treatment of an alkyl halide with sodium methoxide in methanol medium, then there is possibility of…

Q: Which conditions are best for the transformation? но ОН но Link K2Cr207/H2SO4 NABH4 O H20/HCI O…

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Q: 5. Retrosynthesis. Suggest how the molecules mentioned below can be synthesized (give the reagents…

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Q: -CH, CH, HyC

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Q: 3. Give the complete electron flow of the SN1 reaction, be sure to clearly show the electrons that…

A: In both cases there is a common carbocation formed which undergoes SN1 and E1 reaction pathway as…

Q: the  compound  can be synthesized by an SN2 reaction. Suggest a combination of haloalkane and…

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Q: Suggest a synthesis for the molecule shown below. Only starting materials containing six (6) carbons…

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Q: 6. Provide a total synthesis for the target molecule starting from benzene using any reagents…

A: (a) When acetone is treated with phenyl magnesium Bromide (Grignard reagent) then 2-phenyl -2-…

Q: Using the curve arrow symbolism, provide a step by step mechanism that accounts for the…

A: Here, polar protic solvent water is present. That's why under heating condition SN^1 mechanism is…

Q: Suggest a synthesis for the molecule shown below. Only starting materials containing six (6) carbons…

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Q: QUESTION Complete the following synthetic transformation by selecung from the list of reagents below…

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Q: 5. Provide a complete curved arrow mechanism for the most straightforward conversion of 5 and 6 to…

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Q: Show how HC ≡ CH, CH3CH2Br, and (CH3)2CHCH2CHBr can be used to prepare CH3CH2C ≡ CCH2CH2CH(CH3)2.…

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Q: 2) Rank these molecules by their SN2 reaction rate. If a difference in reaction rate is hard to…

A: The correct order of molecules towards SN2 reaction is   D > E > A > C > B.   The order…

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.