draw out the mechanism of the following reaction. be sure to draw all intermediates and use arrows to show the flow of electrons: GTP + IMP + L-Asp-> GDP + phosphate + N6-(1,2-dicarboxyethyl) - AMP
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- Look at the reaction given, the product is 9,10-anthraquinone. Please draw a mechanism for another possible structure from the reaction, emodin. -OH IL,SO, A CFor the compounds shown below, identify the two beta hydrogens and give the major Hofmann elimination product. a) CH2CH3 CH3 ОН CH3 H3C b) O N(CH3)3 OH-SHOW/IDENTIFY the arrow pushing mechanism in at least 4 steps. CH,OPO?- | 3* C=0 2 HO-CH2 1 CH,OPO | 1 C=0 2 Dihydroxyacetone phosphate (DHAP) Но—С H 3 aldolase + Н—С-—ОН H Н-С-—ОН 15 CH-ОРО 6. Н—С—ОН CH,OPO Fructose- 1,6-bisphosphate (FBP) Glyceraldehyde- 3-phosphate (GAP)
- CO,Et CO,Et (28) product. Draw the product of the following reaction. Several diastereomers can be obtained; draw the one lowest in energy, which is the major NC CN Solve cat. base Start forum topic HC CH3 (29) workup, a new compound is formed. Draw it. When the product of the previous reaction is heated in dry EtOH that contains excess NaOEt, and the product is subjected to aqueous Solve Start forum topicShow the complete mechanism of the acidification of disodium adipate and calculate pKeq for both protonation steps. Note: pKa1 = 4.0, pKa2 = 4.4 for adipic acid. A mechanism must show all nbe’s and show movement of e’s with curved arrows.3. Propose a mechanism for the following Aldol addition and beta elimination. 1) 1.1 equiv LDA, -78C 2) To the H 3) H3O+, heat
- Draw Intermediate CH3OH₂+ protonation H H3C -0 H Q CH3OH deprotonation loss of H₂O elimination H3C :0 ÖH -CH3 Draw Intermediate CH3OH deprotonatio Please select a drawing or reagExplain the following stereochemical outcome. Draw structures of key transition states and clearly show the direction of attack by nucleophiles or electrophiles. OH racemic SAE (-)-DET OH TRASE OH Draw the correct stereochemistry at each chiral centerComplete the following reaction of hydrolysis using arrows and drawing the intermediate products Catión estabilizado por resonancia Catión oxonio MeO OMe - MeOH R R Acetal Catión oxonio Catión oxonio Meo OH R- R Hemiacetal MeOH Catión estabilizado por resonancia -H® R R Compuesto carbonilico