Suggest a suitable and possible synthetic method to design the following organic compounds. and I want to now the name plz and the step of the mechanism plz CH3 CH3 ZI
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A: Basic concepts of Organic chemistry.
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Q: Suggest a synthesis for the following compound from the indicated starting materials and an other…
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Q: Outline a synthesis of 3-ethyl-2-methyl-2-pentanol from starting materials of 3 carbons or less.…
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Q: 1. HNO3, H,SO, 2. Fe, HCI 3. NANO,, HCI 4. HBF, 5. KMN04, A CH(CHS2
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Q: Examine the sequence of reactions shown below and provide structures (including stereochemistry…
A: The given reaction sequence is represented as follows:
Q: Show the electron-flow mechanism of the synthetic schemes (Aniline) of the picture below. This…
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Q: Predict the product for the following synthetic sequence. 1) H,O+ 2) Na,Cr207, H2SO4 , H20 3) PhMgBr…
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Q: i) Give the IUPAC name of this molecule. ii) Outline the mechanism of this reaction. Your mechanism…
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A: The structure of dihydropyran is; The structural formula of dihydropyran is C5H8O. The…
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Q: Suggest a retrosynthesis and a synthesis for one (1) of the following compounds starting…
A: The image of the mechanism is been uploaded in step 2.
Q: Suggest short, efficient reaction sequences suitable to produce the compound from the given starting…
A: Benzyl methyl ether can be prepared by the reaction of benzaldehyde dimethyl acetal and…
Q: Predict the product for the following synthetic sequence. 1) H30* 2) Na2Cr,O7 , H2S04 , H2O ? 3)…
A: The reaction taking place is given as,
Q: How can you obtain iodoethane from ethanol when no other iodine containing reagent except NaI is…
A: Ethanol reacts with hydrogen chloride in presence of zinc chloride to give ethyl chloride. Further,…
Q: A compound X on reductive ozonolysis gives ethanal, methanal and carbon-dioxide. X is
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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: -Chlorination of aniline CaHsNH2 produces (a) Para chloro aniline (b) Meta chloro aniline (C) Ortho…
A: The reaction of Aniline with Cl2 gives 2,4,6 trichloro aniline. i.e. Mixture of Ortho and Para…
Q: The etner ring in solamin is blosyntnesized from the diene as shown pelow. Suggest a mechanism for…
A: Due to technical error ,unable to provide you the solution. Please resubmit the question once again
Q: Over the past several decades, chemists have developed a number of synthetic methodologies for the…
A: Retrosynthesis analysis gives (2) and (3).
Q: Provide a plausible arrow pushing mechanism for the reaction below. 1.1 eq. tBuOK 2. acidic workup
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Q: 5. Provide all the missing products (A-C) and reagent (i). Suggest retrosynthetic analysis for this.…
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Q: Over the past several decades, chemists have developed a number of synthetic methodologies for the…
A: There are four chiral centres in the estrone that are marked in the structure below,
Q: How to prepare the following compound by Retrosynthesis (RSA) and functional group interconversion…
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Q: Over the past several decades, chemists have developed a number of synthetic methodologies for the…
A: The stereo selective double Heck reaction of arene (1) is highly efficient strategy to prepare the…
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Q: Using suitable disconnection strategles, suggest plausible synthetic plans for the followtng…
A: Retrosynthetic Analysis: Imaginary breaking the bond into the workable reagents that can be combined…
Q: Over the past several decades, chemists have developed a number of synthetic methodologies for the…
A: There are two functional group present in the Estrone. 1. Alcohol 2. Ketone
Q: a) Consider the substitution reaction shown below: n-Pr. Me Br Et organic product + H-Br H2O i)…
A: Since, you have posted multiple sub-parts for this question , we will solve the first three…
Q: nthesize the following compounds: 2,2,4-Trimethylpentane from two halogenated derivatives of four…
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Q: Give five (at least) different synthetic routes (different type reaction to prepare benzoic acid…
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Q: Below, depicts the electron flow process for the synthetic schemes. This should include the…
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Q: Using diagrams draw a full retrosynthetic sch
A: Retrosynthesis is a process of deconstructing a target via disconnections of bonds LiAlH4 is…
Q: Reaction of 2-chlorobutane with CH;CH2OH will produce three products which are compound F, G and H.…
A: The reaction between 2-chlorobutane with CH3CH2OH then that will give F, G, and H.
Q: Over the past several decades, chemists have developed a number of synthetic methodologies for the…
A: Compound (2) has the aromatic ring that becomes ring A of estrone. Compound (3) has fused six and…
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A: Sn2 reaction is favored in nonpolar solvent.
Q: Suggest a synthesis for the molecule shown below. Only starting materials containing six (6) carbons…
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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. Outline the synthesis route for the product. Any appropriate reagents such as carboxylic acid or…
A: Note : The groups on benzene ring direct the electrophile to ortho, para or meta position. Step 1:…
Q: Suggest a synthesis for the following compound from the indicated starting materials and any other…
A: Since, you have multiple questions. So, I will solved first question for you. You can see the…
Q: 4. Answer the following questions based in the scheme below: (i) Determine the principle involved in…
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Q: 2. Devise reactions schemes to carry out the following multi-stage processes to make ethyl ethanoate…
A: Interpretation - To make ethyl ethanoate from using the ethanol as the organic reagent - To make…
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- Acetoxybenzene (PhOC(=O)OCH3) is much less reactive than ethoxybenzene (PhOCH2CH3) in electrophilic aromatic substitution reactions. Suggest an explanation for this result, based on an analysis of the inductive and resonance electronic effects of the two substituents on the stability of theWheland intermediate for para substitution by an electrophile E+Suggest ways of synthesizing the compound, how would youmake the disconnections and what are the synthons?One of the products of petroleum refinery is naphtha where, benzene could beobtained via catalytic reforming of naphtha. The obtained benzene can potentiallyto react with Lewis acid to form new carbon-carbon bond. Propose the startingmaterial and stepwise mechanism to produce new chemical structure which consista formula molecule of C11H16.
- Provide a mechanism for the following isomerization in aqueous acid. Thank you in advance!In an aqueous solution containing sodium bicarbonate, aniline reacts quickly withbromine to give 2,4,6-tribromoaniline. Nitration of aniline requires very strong conditions,however, and the yields (mostly m-nitroaniline) are poor.(a) What conditions are used for nitration, and what form of aniline is present under theseconditions?Use your knowledge of directing effects, along with the following data, to deduce the directions of the dipole moments in aniline and bromobenzene.
- Illustrate the mechanism of forming alkynes from a 1,2-dihalide and a vinylichalide. Show intermediates as applicable and use the arrow formalisms.Organotin compounds play a significant role in diverse industrial applications. They have been used as plastic stabilizers and as pesticides or fungicides. One method used to prepare simple tetraalkylstannanes is the controlled direct reaction of liquid tin(IV) chloride with highly reactive trialkylaluminum compounds, such as liquid triethylaluminum (Al(CzHs)3). 3SnCl4 + 4Al(C2H5)3 → 3Sn(C2H5)4 + 4AlCl3 In one experiment, 0.160 L of SnCl4 (d= 2.226 g/mL) was treated with 0.346 L of triethylaluminum (Al(C2H5)3); d = 0.835 g/mL). What is the theoretical yield in this experiment (mass of tetraethylstannane, Sn(C2H5)4)? If 0.257L of tetraethylstannane (d= 1.187 g/mL) were actually isolated in this experiment, what was the percent yield?Propose a synthesis of the anti-inflammatory drug Ibuprofen from benzene. Show all reagents and all intermediate structures. Assume that ortho and para isomers can be separated