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- In the box to the left of each reaction below, write the mechanism by which it occurs (could be SN1, SN2, or E1, or even 2 of them). Then draw the product(s).Draw the major E2 elimination products from the attached alkyl halides.Alkyl diazonium salts (shown below) are considered "super" leaving groups; a consequence of this is that they tend to be contact explosives What quailities make alkyl diazonium salts such excellent leaving groups?
- In an E1 mechanism the leaving group leaves first to form a carbocation andsubsequently a proton is removed by a base to form the alkene. In an E2 mechanism theproton and the leaving group leave at the same time. The compound shown belowundergoes an Elimination reaction in a two-step mechanism that does not follow the orderor steps as described above (not E1 or E2) a. Draw the mechanism and give the product of the elimination reaction.b. Why do you think this reaction follows this unusual elimination reaction? Support youranswer with all relevant structure(s)In Image 4 predict the effect the substituent attached to the benzene ring would have on electrophilic aromatic substitution reactions? a.ortho/para director, deactivator b.ortho/para director, activator c.meta director, activator d.meta director, deactivatorDraw all products, including stereoisomers, in each reaction.