a) Show using free radical reaction how you can prepare benzyl bromide from toluene. phenylmethanamine from benzyl bromide using b) Show how you would prepare Gabriel synthesis.
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- Alkyl diazonium salts decompose to form carbocations, which go on to form products of substitution, elimination, and (sometimes)rearrangement. Keeping this in mind, draw a stepwise mechanism thatforms all of the following productsAlkyl diazonium salts decompose to form carbocations, which go on to form products of substitution, elimination, and (sometimes) rearrangement. Keeping this in mind, draw a stepwise mechanism that forms all of the following products.how an alkene be coverted into carbonyl compound in one step?
- provide a mechanism to get compound AGive typed full explanation draw the reaction of alcohol alkoxylation using soudim methoxide catalyst: a-what are the bi-products can be formed during the reaction if i conduct the reaction without drying step? explain b-what are the bi-products can be formed during the reaction if i conduct the reaction with drying step? Explaina) Predict the major organic product of the following reaction b) Draw the detailed mechanism (using curved arrows) to show how the major product is produced. Don't forget to include resonance structures! c) Explain how you determined the major product
- Propose mechanism consistent with the following reactions a and b?a. Propose a mechanism for the following reaction.b. Explain why two products are formed.c. Explain why methanol substitutes for only one of the bromines.A student tried to carry out the following reaction sequence, but none of diol A was formed. Explain what was wrong with this plan, and design a successful stepwise synthesis of A.
- Synthesize Chloramphenicol from Toluene or Benzaldehyde. Draw and explain step by step please.(p.s: if you can, can you write what the reagents does?) (Drug Chemistry)(a) Propose a mechanism for reaction A, which is a substitution reaction. (b) Explain why reaction B does not lead to a similar substitution.Propouse a mechanism for the following reaction.