- Show Attempt History Current Attempt In Progress Propose A Plausible Mechanism For The Following Transformation Do Oh 1 1 (29.17 KiB) Viewed 12 times
- Show Attempt History Current Attempt In Progress Propose A Plausible Mechanism For The Following Transformation Do Oh 1 2 (20.4 KiB) Viewed 12 times
- Show Attempt History Current Attempt In Progress Propose A Plausible Mechanism For The Following Transformation Do Oh 1 3 (29.79 KiB) Viewed 12 times
0.33/1 E deprotonation of the alcohot by the strong base. The resulting akoxide anioni Correct. This mechanism begin strong nucleophile and will undergo an S2 mechanism with ethyl iodide. This substitution reaction is expected to be an S 2 mechanism because the leaving group. lodide primary is on a carbon that is Identify the most likely sequence of steps in the mechanism: Step 1: deprotona Step 2: nucleophilic attack Step 3: none (only 2 steps) eTextbook and Media I
Incorrect. NaH acts as a strong base. Which of the four mechanistic steps is shown in this step of the mechanism? Add curved arrow(s) to draw step 1 of the mechanism. Modify the given drawing of the product as needed to show the intermediate that is formed in this step. CH₂ CH₂ OH Edit Drawing Hint