

Kolbe-Schmitt Reaction Mechanism
O 1NGOH, COS OK
answer all parts
Draw the mechanism (electron pushing and main organic product) for the first step of this Kolbe-Schmitt reaction. The Kolbe-Schmitt reaction adds a carboxyl group ortho to the hydroxyl group of phenol. After acidification, salicylic acid is produced. он 1) NaOH OH 2) CO, (100 atm, 125°C) 3) H0 DO A ¢ % o Ć . I I O Z o os Draw the starting material and electron pushing arrows for the third step of this Kolbe-Schmitt reaction....
Question 3 Consider the reaction shown below. CEN ОК KOH H20 Propose a detailed mechanism using curved arrows in a step by step manner to illustrate the formation of the carboxylic acid salt formed in this reaction. Make sure to use curved arrows to show the deprotonation, protonation, bonds formation or bonds cleavage.
What is the product of this reaction?
Br2 Н,0 +enantiomer o Br '+enantiomer ООН + enantiomer о он Br+enantiomer
Draw the major product produced in the following two step reaction. 1) NaOH, CO, 2) Br,, Feci, Hint: Step 1 is the Kolbe-Schmitt reaction (Refer to Question 23). DOCX , RO Ful MacBook All * W A.
1.Draw the mechanism for the following reaction: (8
points)
1.Draw the mechanism for the following reaction: (8 points) COOH heat + b. COOH HBr, leq b. a.
uue Malonic Ester Propose an arrow-pushing mechanism for the following reaction. Name: H₃ Br2 CH,COOH ROH
Find the mechanism
COOH COOH CH3C1 0=0=o=0 KMnO4 conc. HNO3 Anhy. AICI: heat conc. H2SO4 HO NO2 3-nitro benzoic acid benzene toluene benzoic acid Sn/HCI COOH COOH COOH HO NaNO2 + HCI 0°C COH N CI NH2 3-hydroxy benzoic acid 3-chlorodiazenyl)benzoic acid 3-amino benzoic acid
If AGº for a reaction is greater than zero, then__ OK=1 ОК<1 Қ>1
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