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- Please explain how you came about your answer for these questions 1. Identify nucleophiles and electrophiles 2. Name any type of reactions taking place like E2 or E1 3. Account for any regio- or stereoselectivity... Show full machanism formation of productplease quickly thanks ! 3.Please write out the major reaction and side-reaction in the preparation of ter-butyl.chloride, and write out the key points to use separation funnel in this process.
- Select reagents from the table to carry out this transformation in 5 steps.What is reaction 1 and 2 called? Choices: A. Williamson ether synthesis, B. Reduction with Grignard reagent, C. Acidic ether cleavage, D. FC Alkylation What are the reagents for reaction 1 and 2? Choices: A. methanol in acidic medium, B. sodium hydride and bromomethane, C. methyl bromide and aluminum bromide, D. methanoyl bromideShow the steps to make 5 undecene from acetylene and any other reagents? (More than one step may be required)
- In each reaction box, place the best reagent and conditions from the list below.Any help with this would be great! Explanations definitely welcome, thanks in advance for any help:) What is the major product of the reactions?Why doesn't iodoethane react via Sn2 with NaI in acetone? It is a good leaving group and it is on a primary carbon. I know it is able to react Sn1 quickly.