PROBLEM Propose a mechanism for the acid-catalyzed conversion of cyclohexanone to 2-chlorocyclohe TH CH,COOH cyclohexanone 2-chlorocyclohexanone...
Propose a base catalyzed tautomerization mechanism for the keyo to enol conversion of guanine.
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 for the acid catalyzed hydrolysis of the following imine.
Provide the product for the following reaction. Propose an acid catalyzed mechanism for this reaction. Specify if this reaction is general acid or specific acid catalyzed reaction. Draw free energy diagram for this reaction based on your mechanism. Make sure to include reaction intermediates in your free energy diagram (12 points total) NH 2 pH 3
Please show the mechanism with acid. 2. Write the complete reaction mechanism for the KCN-catalyzed reaction. Show all electron flow with arrows and show all intermediate structures он CH-COOH O но CN = C H20* Who. HHCEN NAOH HO cyanolydrin + NaCN + H2O
The following compound results from base-catalyzed aldol cyclization of a 2-substituted cyclohexanone. Starting with the diketone, propose a mechanism for the cyclization. o
Predict the major product of the acid-catalyzed dehydration of 2,2-dimethyl-1-hexanol. Then propose a mechanism with curved arrows of this reaction. 20) Predict the major product of the acid-catalyzed dehydration of 2.2-dimethyl-1-hexanol. Then propose a mechanism with curved arrows of this reaction. H2SO4 LOH heat
Write a full mechanism for the acid catalyzed conversion of acetone into irs corresponding enol. Draw all of the possible resonance structures for each of the following 0 0 0 Hi Hi Ho 2009 b. Write a full mechanism for the acid catalyzed conversion of acetone into its corresponding enol. c. Draw all of the possible resonance structures for each of the following:
uue Malonic Ester Propose an arrow-pushing mechanism for the following reaction. Name: H₃ Br2 CH,COOH ROH
Propose a stepwise mechanism for the following acid catalyzed reaction. НО Н,0*, Н,0 НО,