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A: The solution is given below -
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Q: Show how to Synthesize fon benzene and meassoy reagents:
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Q: Show how cyclohexanecarboxylic acid could be synthesized from cyclohexane in good yield. -COOH
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Q: エZ
A: Here we have to synthesize the given compound by suitable starting materials.
Q: Show how to synthesize the compound from benzene.
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Q: NH Phthalimide
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Q: OH
A: Ans is govt below
Q: Predict
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Q: Which of the following carbonyl compounds has the most acidic hydrogen? Show why it has the most…
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Q: Br
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Q: ОН
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A: The synthesis of muscalure from acetylene is given below.
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Q: Show how you would synthesize octanal from each compound. You may use any necessary reagents.ethyl…
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Q: OH
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Q: Propose a synthesis of the following product beginning from benzene. HN.
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Q: Devise a synthesis of the following compounds starting from benzene.
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- w how enols, enolate ions, andenamines act as nucleophiles. Predictthe products of their reactions withhalogens, alkyl halides, and otherelectrophiles. Show how they areuseful in synthesis.predict the stating materials, reagents, or products of the followinf reactionsAcetoxybenzene (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+
- Suppose you have compounds A–D at your disposal. Using thesecompounds, devise two different ways to make E. Which one of thesemethods is preferred, and why?give reactions and intima mechanism of following reactions-Enamines formed from the cyclic secondary amine pyrrolidine are important intermediates in the synthesis of 1,5-diketones. (1st pic) On the structures provided below, draw arrows showing electron flow for the reaction mechanism for the acetic acid-catalyzed formation of an enamine from cyclohexanone and pyrrolidine. (2nd pic)
- Give synthesis of longifolene by e.j coreyWhich reagent(s) sequence(s) is/are optimum for preparing butanoic acid from 1-propanol? i. K2Cr2O7 in acidii. (1) PBr3; (2) NaCN; (3) H2O; (4) [H+] iii. (1) NaCN; (2) H2O; (3) [H+]iv. LiAlH4Compounds A, B, and C have the same molecular formula C4H8. They all react wotu H2/PtO2 to give the same compound. The reaction of A or B with H2O/H2SO4 or with BH3-THF, followed by treatment with a basic solution of hydrogen peroxide, gives the same compound, namely D. The reaction of C with H2O/H2SO4 also gives D. However, the reaction of C with BH3-THF, followed by HO-, H2O2 gives a new compound, E. Provide the identity of A, B, C, D, and E along with explanations of reactivity.
- 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.Predict the major organic products for subparts e, f, g, h, i, jCompound A gives the product(s) below on oxidative cleavage with KMnO4 in acidic solution. Propose a structure for A.