Give a detailed mechanism for the reaction utilizing 1-butanol and acetic acid.
Give a detailed mechanism for the reaction utilizing 1-butanol and acetic acid.
3. Show the detailed mechanism for the Fischer Esterification reaction between acetic acid and sec-butanol. All arrows, charges, structures, etc must be shown neatly and clearly - every little detail counts!
What is Zaitsev’s rule? Give the mechanism for the acid-catalyzed E1 reaction of 2-butanol. Give the mechanism for the base-catalyzed E2 reaction of 2-bromobutane. Draw all possible products. You expect three products from the elimination reaction 2-butanol. What are they? The E2 mechanism is a one-step mechanism. True or False? Explain. Which of these two alcohols would you expect to be more reactive under H3PO4/aqueous conditions? Why? Give the structure of the main product in both cases. 1-phenyl-1-propanol 1 -cyclohexyl-1-propanol...
Create a step by step mechanism for 1-butanol reacting with acetic acid to form butyl acetate. Under what circumstances would the equilibrium lie to the right? To the left?
Write a detailed reaction mechanism for the reaction between 2-methyl-2-butanol and concentrated HCl. If 2-methyl-2-butanol was treated with concentrated H2SO4 instead of concentrated HCl, what product would predominate?
Draw the detailed SN1 mechanism for the reaction between 2-methyl-2-butanol and HCl to produce 2-chloro-2-methylbutane. 1. Draw the detailed Sn1 mechanism for the reaction between 2-methyl-2-butanol and HCl to produce 2-chloro-2-methylbutane. (3 pts)
Carboxylic Acids and their Derivatives. 1. For the reaction below, give a detailed mechanism for both an acid-catalyzed and base-catalyzed reaction. (2pts) + CH OH IN Acid Catalyzed Mechanism: Base-Catalyzed Mechanism: 2. How would you carry out the following syntheses. (4pts) CN
1-Butanol reaction with sodium bromide and sulfuric acid. Draw the reaction mechanism. Explain why the reaction would prefer a polar protic solvent.
7. Provide a detailed mechanism for the reaction 2,2-dimethylcyclohexanol with phosphoric acid. Give the major product and do not forget the charges and arrows. (4 pts.
7. Provide a detailed mechanism for the reaction 2,2-dimethylcyclohexanol with phosphoric acid. Give the major product and do not forget the charges and arrows. (4 pts.)
I need help with drawing out the detailed mechanism of NaBH4 reacting with acetic acid to produce triacetoxyborohydride.