Complete the reaction 1.NaOEt 2.Ho* 1. NaOCH3 2. o o* o 1.NaOCH3 o 2.H30* Perform the...
Need Help. Will Rate If Complete.
1) NaoEt, EtOH Br 2) O 3) H30+ / A. 1) NaoEt, EtOH (s) ar 2) Y Br 3) Hz0+ / A 1) NaOme/MeOH ~ Br OMe 3) Hz0+/A. 1) NaOEt, EtOH 2) V Br 3) NaOEt, EtOH COOEt 5) H30+/A Robinson Annulation NaoEt, EtOH/A come lui OMe 28- The following molecules can be formed by either: Michael Reaction; Enamine Acylation; Acetoacetic Ester Synthesis; Michael Addition; Malonic Ester Synthesis; Robinson Annulation; Aldol Condensation; Claisen...
(1) Show the product of each alcohol oxidation reaction below: OH Croz H30", acetone PCC CH2Cl2 OH Cr₂O, OH H.SO 4, H2O PCC HO CH2Cl2 Nag H2S04, H20 (2) Propose an efficient synthesis for each transformation below mocow OH НО? .name مل.بلو HO / تم.-م" (E) Ph amion e no (F) OMe
le
chatelier experimen
Thursday). 1. What starting material and reagents are needed for the following multi-step synthesis (HINT: aldol reactions work best when the starting material can only form one enolate)? 5 он о D. NaOH, H2O, Heat F. HO E. NaOH, H2O G. LDA Starting Material: Reagents: 2. LDA is a strong, sterically hindered base and will form the enolate. Sodium hydride is a weak base and will form the _ - enolate. Kinetic enolates are the stable and...
Predict the product for the following reaction sequence. H30+ 1. NaOCH2CH3 2. CH3CH2CH21 A HO HO = OH IV
1. NaOEt CO2Et 2. H30+ 3. heat Br. Br CORET + H3C V CO2H H₂C + CO2 + E H3C CO2Et The malonic ester synthesis is a carbonyl alkylation reaction. It is used to prepare carboxylic acids from primary alkyl halides, lengthening the carbon In progress by two atoms. Thus, the product can be visualized as being a "substituted acetic acid." The reaction consists of three steps: generation of the enolate anion followed by SN 2 reaction with a primary...
major product of the reaction below would be... OEt 1) NaOEt 2) BrCH2CH2CH3 3) H30, heat Select one: O a. ОН ob. DH OC O= Od
Predict the product for the following reaction sequence. 0 H30+ 1. NaOCH2CH3 2. CH3CH2CH21 HO HO = OH IV
Predict the major organic product of the following reaction and complete its mechanism below. 1) NaOEt/EtOH 2) CH3CH2CH2Br 3) dilute NaOH/heat 4) H30* 5) heat Complete the curved-arrow mechanism for the scheme below by adding any missing atoms, bonds, charges, nonbonding electrons, and curved arrows. :O O: :Br. CH3CH2OH Do not show curved arrows for this step. Added acid Dilute HH NaOH and heat hydrolyzes the ester. O: Na Br - H20, Na* O: 100-150 °C O:
1) Me 2 Culi 2) H30* What is the major product of the reaction? 요 o OH NaCN HCI What is the major product of the above reaction? No reaction HO CN CN NEC TSOH NH2 What is the major product of the above reaction?
7. (10 pts) Predict the major product and show the mechanism for the following reaction 1. OH 2. H30+,a (5 pts) Provide a synthesis of the following compound using ammonia (NH) 8.
7. (10 pts) Predict the major product and show the mechanism for the following reaction 1. OH 2. H30+,a (5 pts) Provide a synthesis of the following compound using ammonia (NH) 8.