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- Q4. Nucleophilic attack at carbonyl with loss of carbonyl oxygen. For this question, answer AT LEAST FIVE of the SIX parts. (a) For the FOUR reactions listed below, draw structures of the major organic products. (i) (ii) (iii) HO OH ●... NMe₂NH₂ cat. dry HCI H Ph₂pⓇ THFI'm stuck on step 3. Please help, thank you9) a) Diagram the acid (H3O+) catalyzed enolizaton of acetaldehyde. . b) Diagram the base (OH-) catalyzed formation of cyclopentanone from its enol form.
- Please don't provide dand written solution...Please help mePreamble: A student chemist in an attempt to synthesise compound B from the aromatic aldehyde. 24. What is the reaction name for the chemical transformation of A to BA. reductive aminationB. catalytic reductionC. carbonyl dehydrationD. Hofmann eliminationE. Aldehyde rearrangement
- Please help me with the organic chemistry question below: 1) Show the mechanism for the linkage of two pyrroles with a benzaldehyde.b) Esters can undergo hydrolysis to give an alcohol and a carboxylic acid. Lactone P which is a cyclic ester, can undergo base-catalyzed hydrolysis to give a hydroxy carboxylic acid. Write the plausible mechanism for the transformation.Add arrows indicating the flow of electrons and identify the steps in the mechanism below. H. Ö: H. H. HO: HO: H. H. н H. он HO. H. H. H. H. H. 1) What is purpose of the acid in the first step of the mechanism? 2) How does this help the water react with that intermediate?
- 4) We discussed in class how acetals are formed from a ketone and two equivalents of an alcohol, using an acid catalyst. Alternatively, would a strong base also catalyze (i.e. accelerate) the formation of an acetal? Explain why or why not, in the context of the reaction mechanism and potential intermediates. Naome, MeoH าาาา ← meo ome + HzoPlease answer the following pertaining to organic chemistry.Complete the following generic reaction mechanism for carboxylic acid derivatives under the indicated conditions. 1) Acidic Conditions HNuc Z. 2) Basic Conditions :Nuc Z. 3) Neutral Conditions :NH3 Z.
