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- A student proposes the following reaction mechanism for the reaction in Model 6. Which step inthis mechanism is least favorable? Explain your reasoning.For which reaction mechanisms—SN1, SN2, E1, or E2—of thefollowing statement true? A statement may be true for one or moremechanisms. The reaction rate increases with better leaving groups.Can you provide a mechanism for this reaction to show the major diastereoisomer that would be formed?
- What are the major product(s)? Show the mechanism.For the following dehydrohalogenation (E2) reaction, draw the Zaitsev product(s) showing the stereochemistry clearly. If there is more than one organic product, both products can be drawn in the same box.Rank the following substrates in order from slowest SN1 reaction rate to fastest:
- What is an appropriate multi-step method/mechanism for the transformation shown in the image?? (One of the steps involved here can also be found at the end of Baylis Hillman and Rauhut-currier reactions. The red&green dots show where C from the beginning is now found in the end product.)For the dehydrohalogenation (E2) reaction shown, draw the major organic product, including stereochemistry.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).
- Shown below are two reactions; Reaction 1 is a Friedel-Crafts acylation while Reaction 2 is a Friedel- Crafts alkylation. State which reaction will occur faster and justify your answer, with words and structures. Mention: e- density / Deactivation / Resonance stable / faster the carbonation formed because it's gonna have smaller activation energyDescribe the predominant mechanism( SN1, E1, SN2, E2) in the following reaction to draw the major product(s).Write whether it will be E1, E2, SN1, and/or SN2. Or both. Show the mechanism(s) Write the MAJOR product(s) State the stereochemistry of the product(s), when applicable.. please do them in the form provided .