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A: The synthesis of the above given product from toluene and other compounds is given below :
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A:
Q: (b)
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A: Given reaction:
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A: Heck Reaction is a cross-coupling reaction of an organohalide with an alkene to make a substituted…
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A: In this question we will synthesized the given compound by using benzyl bromide You can see details…
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A: The given starting material which has to be converted to an epoxide is as follows,
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A: Given compound: We have to synthesize the above compound from benzene.
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A: To determine which reagents could be combined to make below compound
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Q: NH2 (Benzyl amine) (a) H.
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Q: CH
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A: This reaction is carried out in polar aprotic solvent like DMSO
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A: Gilman Reagent is the Lithium dialkylcuprate. It is used for the formation of C-C bond.
Q: I
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A: Major product in this reaction:
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A: Given compound: We have to synthesize this compound from benzene.
Q: ОН HO СООН C-OCH3
A: There is the conversion of o-hydroxybenzoic acid to o-hydroxyacetophenone.
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- Given what's provided, what product forms?Treatment of 1,2-dibromoethane with the dithiolate dianion shown in the reaction below leads to two products as shown. Draw the structure for each molecular formula and provide a detailed mechanism for the formation of both products.For each reaction, predict what mechanism will account for the major product(s) formed and write (SN1, SN2, or NR) in the boxes provided. Explanations or drawings are not required.
- Identify the leaving group for a potential elimination of the following compounds. Compare the leaving group activities for A and K. Which of the following compounds cannot be subjected to elimination? Explain.Which of the following molecules will NOT lead to a successful synthesis of a Grignard reagent upon reaction with magnesium? CI https://ibb.co/54Jw34p 2 Me. OMe https://ibb.co/6655LTH Br но https://ibb.co/2nfzPmX O Me `Br https://ibb.co/wo93ymS 2 Br MeO https://ibb.co/Hq2s6ck 2When phosgene is treated with excess methanol, a product is formed whose "H NMR spectrum shows one peak-a singlet at 3.8 ppm. Provide a complete, CH,OH ? CI CI detailed mechanism for this reaction. Phosgene