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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- One of the later steps in glucose biosynthesis is the isomerization of fructose 6-phosphate to glucose 6-phosphate. Propose a mechanism, using acid or base catalysis as needed.Draw complete mechanisms with electron flow for the following reactions.Which of the following bases are strong enough to deprotonate CH3CH2CH2C≡CH (pKa = 25) so that equilibrium favors the products: (a) H2O; (b) NaOH; (c) NaNH2; (d) NH3; (e) NaH; (f) CH3Li?
- PQ-22. Which structure is a reasonable intermediate in the acid-catalyzed hydrolysis of ethyl acetate, shown, in dilute aqueous acid? O O (A) H3C-C-OCH₂CH3 OH OH₂ (C) H3C-C-OCH₂CH3 H OH (B) H3C-C-OCH₂CH3 OH2 O (D) H3C-CPlease write the mechanism of all reactions and show the products stereoisomericallyLook 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 C
- Predict the organic product for the reaction. OH K₂Cr₂O7 H₂SO4 :ÖH acetone Select Draw Templates More H₂CrO4 |||||||CH 0 Add four curved arrows to complete the intermolecular mechanism that forms the oxidized product. Note that potassium dichromate in acid is in equilibrium with chromic acid used. 3 Select Draw Templates More H H 0: C H H Cr 0 : OH Q : 0:9. Draw an arrow pushing mechanism for the following reaction. You may use generic HA and A: as needed to carry out proton transfer steps. HO HO OH OH OH Yoga fyty (2 equiv) H+ HOWhich of the following bases are strong enough to deprotonate C6H5OH (pKa = 10) so that equilibrium favors the products: (a) H2O; (b) NaOH; (c) NaNH2; (d) CH3NH2; (e) NaHCO3; (f) NaSH; (g) NaH?