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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).3) Explain how and why the reaction below results in the observed regiochemistryand/or stereochemistry.Can you do 3 and 4 and explain it? And how yo identify it. State the mechanism in which through reaction proceeds sn2 or sn1
- Complete the following reactions with the majority products and the missing reaction conditions. Indicate stereochemistry if applicable. Also indicate the type of reaction that took place (SN1, SN2, E1, E2, E1bc)Draw all possible alkenes that could be generated from an E2 elimination reaction of 3-bromo-3-methylhexane. Suggest conditions that can be used to make just one of the alkenes in a controlled manner (i.e., conditions that would lead to formation of just one alkene as the major product).Write whether it will be E1, E2, SN1, and/or SN2 Show the mechanism(s) Write the MAJOR product(s) State the stereochemistry of the product(s), when applicable Please do them how i set them up.. that the only way I understand.
- Predict the product, draw the mechanism, and plot the reaction coordinate diagram for theE1 reaction.Provide the mechanism for the conversion shown below. CH3Li is effectively H3C-Li+. What type of mechanism is occuring?Explainwhythefollowingdeuterated1-bromo-2-methylcyclohexaneundergoes dehydrohalogenation by the E2 mechanism, to give only the indicated product. Two other alkenes are not observed.
- Between E1 and E2, which reaction mechanism is most efficient to synthesize the (E) stereoisomer of this product on an industrial scale?Draw the arrow-pushing mechanism and propose the products. When appropriate, make sure to indicate the appropriate stereo-/regio-chemistry of the product(s). Note that the mechanism(s) by which the product(s) form in reactions A and B are shown in pink. For Reactions C, D, and E you need to deduce the mechanism by carefully analyzing yout reagents and conditions.Please help with the following ochem mechanisms.... 1. Provide the stepwise mechanisms for the following reactions (see attached picture)