3. Indicate the nucleophilic group and the electrophilic group in each of the following reactions, then...
3. Indicate the nucleophilic group and the electrophilic group in each of the following reactions. then draw curved arrows to show the electron flow: H H-N: H-CI: Н (a) H-N H Н (b) HJ - :0: :O: (c) Cl: Cl-APCI: C : H-CI: A-CI: CF: 4. The following reaction has a small, positive AG and takes place slowly at room temperature:
3. Indicate the nucleophilic group and the electrophilic group in each of the following reactions, then draw curved arrows to show the electron flow: (a) H- N H -CH: (D) - (C) NH :CI: CI-APë: :CA: 1-ci: A-CI: 4. The following reaction has a small, positive AG and takes place slowly at room temperature: H3C-CI H-OH - H3C-OH - H-CI (a) The mechanism for the reaction is shown below. Which bond is being broken in the slowest step? Which bond...
16. For each of the following reactions, indicate the nucleophilic center and the electrophilic center. Draw curved arrows to indicate the movement of electrons and draw the reaction products. (a) carbonyl phosphate + ammonia carbamic acid + P : NH HO OPO,?- (b) NADH + acetaldehyde ethanol + NAD H R- NH H. CO -NH2 (c) 2 amino aciddipeptide + H20 NH NH
Draw curved arrows for each step of the following reactions and indicate the type of curved arrow drawn (e.g nucleophilic attack, hydride shift, etc.). Please solve and explain. Thank you. 2. Draw curved arrows for each step of the following reactions and indicate the type of curved arrow drawn (e.g. nucleophilic attack, hydride shift, etc.) (8 pts). B: OH Li-Me
Provide a step-by-step mechanism to account for the product of each of the following reactions. Show the structure of each of the intermediates and use curved arrows to indicate electron flow in each of these steps. 3. Provide a step-by-step mechanism to account for the product of each of the following reactions. Show the structure of each of the intermediates and use curved arrows to indicate electron flow in each of these steps. a) NaOEt (1 equiv) EtOH O OH...
In carbonyl condensation reactions, the carbonyl is neither electrophilic nor nucleophilic both electrophilic and nucleophilic electrophilic nucleophilic Question 20 Give the major product of the following sequence of reactions: 1) HNOZ/H2SO4 acetophenone 2) H/Pd p-aminoethylbenzene m-aminoethylbenzene m-aminoacetophenone m-nitroacetophenone MacBook Pro DD DOO 80 DII FS F7 F4 FS & 7 * oC 6 9
In carbonyl condensation reactions, the carbonyl is neither electrophilic nor nucleophilic both electrophilic and nucleophilic electrophilic nucleophilic Question 20 Give the major product of the following sequence of reactions: 1) HNO/H2SO4 acetophenone 2) H/Pd Op-aminoethylbenzene m-aminoethylbenzene m-aminoacetophenone m-nitroacetophenone MacBook Pro COO 80 DIN FB DOO F7 F9 F6 FS % & * < CC 7 8
Use curved arrows to indicate the flow of electrons for the following elementary steps. label each step of the proper name such as Sn2, E2, electrophile elimination, bond dissociation, coordination, nucleophilic addition, electrophilic addition, or nucleophilic elimination These are the answers I had but they are incorrect... could you explain which are correct? 4. Use curved arrow to indicate the flow of electrons for the following elementary steps. Label each-st with a proper name such as S 2, E2, electrophile...
For the reactions below, name each as either nucleophilic attack. electrophilic attack, rearrangement proton transfer, or loss of leaving.group. chose the correct answer set? Select one: a. Rearrangement, electrophilic attack, nucleophilic attack b. Electrophilic attack, nucleophilic attack, rearrangement c. Nucleophilic attack, proton transfer, loss of leaving group. d. Loss of leaving group.proton transfer, rearrangement. e. Electrophilic attack, proton transfer, loss of leaving group.
3. Show the complete mechanism for the following nucleophilic aromatic substitution reaction. Use curved arrows to indicate the direction of electron flow. Cl OH KOH + KCI NE 0