1. a) Predict the major organic product of the following reactions: b) H₂C c) Br ol Br 1. 1. Mg /diethyl ether ū 2. 3. H/H₂O 1. Mg/diethyl ether 2. 3. H/H₂O Mg 2. H/H₂O H Br /diethyl ether
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- Based on Steric Effect and Electron Delocalization Explain: 1. Phenol is not easily attacked by a positive reagent as aniline 2. Solubility of acetylinic compound in may bases Please do answer all question for an upvote!! Thank you!select the most appropriate reagent(s) to effect the change. K2Cr2O7, H+ H2, Pd 1. Disiamylborane, 2. HO–, H2O, H2O2 NaOCl H2SO4, HgSO4a) Write out the first 3 steps only(to the tetrahedral intermediate shown) in the 6-step arrow pushing mechanism showing how ethyl propanoate is hydrolyzed in acid to form propanoic acidand ethanol. b) NaOH/H2O also serveto hydrolyze an ester; briefly explain why NaOH/H2Ois generally preferable.
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