5. Draw the mechanism for the acetal formation. You MUST show all electron flow.
Show the complete mechanism for the formation of malachite green, including all electron flow.
Draw the full mechanism (using arrows) of the formation of the cyclic acetal when 5-hydroxy-3-methylheptanal reacts with one molecule of ethylene glycol in acidic conditions. First, a hemi-acetal will form, and then the cyclic acetal will form.
27. (10 points) Write the complete stepwise mechanism for this reaction. Show all electron flow with arrows and show all intermediate structures. Please identify the acetal and hemiacetal in your mechanism. or 2eq. CH3CH2OH HCl (cat.) CH2
What's the product of this reaction? Show the mechanism for this acetal formation. Hgot 77)
Draw the reaction mechanism for the formation of hemiacetal and the acetal in the acid-catalyzed reaction of propanone with ethanol
Propose a mechanism for acid-catalyzed acetal formation between propiophenone and ethylene glycol. 5. Propose a mechanism for acid-catalyzed acetal formation between propiophenone and ethylene glycol. (5 pts)
Propose a mechanism consistent with the following reactions (you must show all the intermediates and electron flow to receive full credit) (3 x 3-9 pts) 6. HF 9
For the reaction below: Draw the complete electron pushing arrow mechanism to show the formation of the final product shown. Explain every step of your mechanism. Explain why this is a product favored reaction. ii. H30* H20 OH A
Draw the complete electron pushing arrow mechanism to show the formation of the final product shown. Explain every step of your mechanism. Explain why this is a product favored reaction. но*
Which of the following statement is correct about the mechanism of hemiacetal and acetal formation? A. In the hemiacetal formation mechanism, the oxygen on the alcohol uses its lone pair to "attack the carbonyl carbon before the protonation of the carbonyl oxygen B. The carbocation formation is not favored during the hemiacetal formation mechanism, this is why hemiacetal are generally unstable and very reactive C. In the acetal formation mechanism, hydrolysis of water to the hemiacetal carbon center occurs as...