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- Finde a way to produce these products A,B,C starting with Benzolplease show the detailed mechanism for the reaction below.please explain clearly and in detail. thank you! 2-butene reacts with NBS yields and forms two products, 1-bromobut-2-ene and 3-bromobut-1-ene. explain how this happens using mechanisms.
- Plan out a proposed mechanism for the “new” reaction below.Which compounds from 5a-d will react with hydroxide in the fashion shown. Which reaction will be the fastest and slowest? Explain using knowledge of carbonyl chemistry, pka and leaving groups.( complete the reaction with mechanism , do 2st one )
- a,b-Unsaturated carbonyl compounds are susceptible to either 1,2 addition or 1,4 (Michael)addition. Give examples of nucleophiles that would favor each case and explain yourreasoningA. propose the efficient synthesis and the mechanism B. give the products for each step and the final productPlease provide a mechanism for these simple reactions below!
- Reaction of 2° alcohol A with HCl forms three alkyl chlorides, all of which result from rearrangement of the 2° carbocation initially formed. Draw the structures of these products and a mechanism that illustrates how each is formed.provide the mechanism given the product and starting material along with any reagents neededPlease show ALL STEPS of mechanism using reagents NaHCO3, I2, and H2O Give good solution ASAP Thanks