Q: CH3CO3H
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Q: 1. NABH4 CI 2. H,O
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Q: Show how each alkene can be synthesized by a Wittig reaction
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Q: (c)
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Q: e major product of the following reaction.
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A: D will undergoes the rearrangement in intermediate of carbocation.
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A: The details solution for this reaction is provided below in attach image.
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Q: Draw the major product(s) from addition of HBr to the alkene below.
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Q: + `NH,
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Q: Show how each alkene can be synthesized by a Wittig reaction
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Q: 5) Show the complete mechanism for an E2 reaction with 1-bromo-2-tert-butylcyclohexane
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E1 Reaction- Solvolysis gives 5 products. Consider both carbocations and draw all 5 products.
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- 4) Provide the major product for each of the reactions shown below. Watch out for carbocation stabilities. NaOEt EtOH BrYY EtOH heat4) Provide the major product for each of the reactions shown below. Watch out for carbocation stabilities. NaOEt EtOH Bra BrYY EtOH heat4. Draw the reaction mechanism and product for the following reaction. Same HO [H*] Quy
- 4) Draw the complete electron-pushing arrow mechanism for the following reductions. Explain, using resonance contributors, the regiochemistry that results in each case. ỌMe Na, MeOH ? NH3 CHO Na, MeOH ? NH3What is the missing starting material or product? Show stereochemistry and mechanism as needed.Both reagents must work. Both reagents must react (bond with each other). Show all reagents and intermediates from all steps of the reactions until the desired product is reached.
- Draw the products of each reaction. Assume excess halogen is present.What is the major product in the reaction below? Draw the complete curved-arrow mechanism to show the formation of the major product.5. Predict whether each reaction will occur via SN2 or E2 mechanism and draw the product. Write 'NR' if the reaction will not proceed as written. & CH3CI NaCl Acetone KOt-Bu t-BuOH KOt-Bu t-BuOH NaOEt EtOH