The mechanism of the reaction is
Please note: between the two proton the more acidic proton is extracted by water.and the stability of the formed product is the driving force of the reaction.(due resonance stabilization the alpha beta unsaturated ketone is more stable then non conjugate beta-gama unsaturated ketone)
A Create OscerSketch Answer 7 Draw a curved arrow mechanism for the following acid-catalyzed isomerization reaction....
Draw a curved arrow mechanism for the following acid-catalyzed isomerization reaction. You must show all intermediates. (10 points) H H20 Create OscerSketch Answer 8
Draw a curved arrow mechanism for the following acid-catalyzed isomerization reaction. You must show all intermediates. (10 points) H. -H 1 н. H20 Create OscerSketch Answer 8
Draw a curved arrow mechanism for the following acid-catalyzed isomerization reaction. You must show all intermediates. (10 points) H H H20
Draw a curved arrow mechanism for the following acid-catalyzed isomerization reaction. You must show all intermediates. (10 points) Н. H H H20
Draw a curved arrow mechanism for the following acid-catalyzed isomerization reaction. You must show all intermediates. (10 points) 80 - H20)
Draw a curved arrow mechanism for the following acid-catalyzed
isomerization reaction. You must show all intermediates.
서 9氣 H20
Draw a curved arrow mechanism for the following acid-catalyzed isomerization reaction. You must show all intermediates. (10 points) ㅇ 봉 H2O
Determine and draw the structures of compounds A and B only. Do not draw the structure of compound X. Place each structure above its letter. HINT: Both A and B are esters. (10 points) LDA 1. compound B 1. NaOEt A х -78 °C 2. H30* OET 2. CH Br A B Create OscerSketch Answer 7 Draw a curved arrow mechanism for the following acid-catalyzed isomerization reaction. You must show all intermediates. (10 points) 1 H H20 Create OscerSketch Answer...
Question 16 ( 10 points) The following reaction is an isomerization from one acetal to another. Draw a curved arrow mechanism by adding arrows and Intermediates to the drawing shown below. There are three intermediates. Note: if you want to remove a proton you do not need to show a base. You can just "kick it out" H3 CH3 CH3 Cg H180₃ CH1703 C3H1703 CH3 LCH3 CH3 CgH1603 C₂H₂,0₂ Create OscerSketch Answer 16
Write a curved arrow mechanism for the acid catalyzed Fischer esterification of benzoic acid in CH3O*H (that is 0-18 labeled methanol). Show all steps, lone pair of electrons, charges and labeled O atoms through the mechanism.