explain the mechanism in words c Draw the full electron-pushing mechanism (using proper electron-pushing arrows, intermediates,...
please draw the full mechanism with all electron pushing arrows, reactant structures, intermediates, and products for the hydroboration oxidation reaction using 1-octene to prepare 1-octanol.
Draw the complete electron-pushing mechanism for each of the reactions. Please draw the reactants, intermediates (with formal charges), products, and electron-pushing arrows. 1. Draw the complete electron-pushing mechanism for each of the reactions. Please draw the reactants, intermediates (with formal charges), products, and electron-pushing arrows. (6 pts) 2 OH H2O HCI
Notes: A ‘detailed’ mechanism should illustrate all intermediates, by-products, and electron-pushing arrows. The marking scheme is given for each question as a guide; It is subject to minor changes. In class, we learned how to sulfonate aromatic rings by treating them with SO3 and H2SO4. This reaction is reversible. Propose a detailed mechanism for this reverse reaction. Note, catalysts are reactants that are regenerated at the end of a reaction sequence.
1. Draw the complete electron-pushing mechanism for each of the reactions. Please draw the reactants, intermediates (with formal charges), products, and electron-pushing arrows. (6 pts) 2 он +H20 HCI
Neatly draw the step-by-step mechansim (with all electron-pushing arrows) for the electrophilic aromatic bromination of toluene (PhMe) using Br2 and FeBr3. Take a clear photo of your mechanism and upload it as your answer to this question.
9. Provide a proper electron-pushing mechanism (including resonance structures) using curved arrows that describes the monochlorination of p-methyltoluene. (10 pts.) CI-CI + HCI hv p-methyltoluene ci
b Write a mechanism for the reaction using curved arrows to show electron reorganization. Consult the arrow-pushing instructions for the convention on regiospecific electrophilic attack on a double bond. Arrow-pushing Instructions inox tv no H- B Draw the organic product of the following reaction. CH3 meta-Chloroperoxy- benzoic acid • You do not have to consider stereochemistry. • Indicate regiochemistry when relevant. • The aromatic ring, when present, is unreactive in all cases. • Do not draw organic or inorganic by-products....
Organic Chemistry Provide mechanism for reaction while using electron pushing arrows showing all possible intermediates and include the most stable resonance. SbCl5 t-BuCI /t-BuOH CF3 CF3 e:o. :O NH3 reflux NH 2 b) Ci: CO CF3 CF3
Show the full electron pushing mechanism with arrows for the synthesis of p-bromoaniline from aniline. Show any side products NH3 N 'CH3 NH CH HCI, H2O 1) H+, H20 Br2 H3C CH COONa CH COOH 2) 5% NaOH Aniline Acetic anhydride Acetanilide p-bromo acetanilide p-bromoaniline bp 184 oC mp 114 oC mp 166 oC mp 64 oC
4. Provide a stepwise mechanism. Include all intermediates, resonance structures, and electron pushing arrows.(ALL OR NOTHING) HEC CH3 AICI D. HCI 5. (Provide the product(s) or reagent(s) for the following reactions. COM ????? ON 77277 HON C ?????