need help with both questions. 4. Show the structure at the end of each step in...
Need help with all 4 of these synthesis reactions. Br in first question and wants to see all arrow pushing, intermediates and products. Last three just want the numbered reagents and the intermediate products after each step. No arrow pushing. Homework #1 Name: 1. Explain with a mechanism the observation of the given products. (Hint: You will need the full reaction mechonism including all intermediates and reogents, Show the proper use of electron pushing arrows.) HBr 2. Propose an efficient...
how do you solve for these? HOW DO YOU SOLVE THESE QUESTIONS STEP BY STEP MECHANISMS 3. Show a mechanism for the following (Grant Challenge). Hint at end with * if you need it. - this is for the people that want a big challenge and who are already very comfortable with mechanisms. 3. Na2CO3, H, 0 0 4. Propose a synthesis for the following, starting from methanolas your only carbon-based starting material. ool logo Me 5. Classify the following...
Help me please as soon as possible i need the solutions for those questions s, show structures of reac the products for both reactions. a) What is/are the product(s) of the treatment of 3-methyl-1-butene with aqueous acidic What is/are the product(s) of the treatment of 2-methyl-2-butene with aqueous basic KMnO4? b) 36) (3 pts each) Predict the products (name and structure) from reaction of 3-hexyne with the following reagents: a) H2, Lindlar catalyst b) Li in NH3 c) HgSO4, H2SO4...
Can some show me the correct mechanism for the following reactions Predict the major product of the following reaction sequence. 1. CHOH, H 2. NaOCH Br ? QH 3. NaOH 4 H30 کلام علام ال CH || III سلام Br IV
I need help with this. If possible be as thorough as possible. Any explanations would be greatly appreciated. This wasn't covered very well so I'm trying to understand it. (1) Radical bromination- predict the structure of the major and minor products in the overall reaction given below. Provide a mechanism leading to each, using appropriate curved arrow notation, and a termination for your MAJOR and MINOR product selection. Clearly label the initiation, propagation and steps. OVERALL REACTION: Br2 (1 molar...
Draw the structure of the organic product formed when the following compounds undergo the three-step reaction sequence indicated. 1. NaOC2H5, C2H5OH 2. NaOH, H20 3. H30, heat C Н Tools % TH COOHOV Grading Include hydrogen atoms on non-carbon atoms. Chirality is not graded
2. Draw the major organic product for each of the following reaction schemes. (1 pt each) a) POCl3, pyridine HO or H3O, heat b) H3O heat c) 0 1. LDA OEt 2 3. Show the structure of each intermediate and product for the following synthetic scheme. Your answer does not need to show the electron flow with arrows but should have correct formal charges. (2 pts) Co Et 1. NaOEt, EtOH Co2Et 2. H30", heat
Help please provide the reaction conditions and structures of the correct products of the following reactions H@C4304 А Ho, heat heat 420 N42 show stepwise how would you prepare the following Compounds from the provided Starting material and any other organic or inorganic compound. In order to have full credit you must show all of the reaction conditions and the structure of your products in each transformation 04 Oet До => Eto Oet
please help solve For questions 1 - 5. predict the major organic products for the following transformations. Clearly indicate formal charges and stereochemistry if applicable. The use of a squiggly bond is not permitted; all stereoisomers should be clearly indicated for full credit. CHO a) Nah, solvent b) workup a) LDA, solvent b) CH, Br, solvent c) workup a) Nah, solvent b) CH, Br, solvent c) workup CHO a) NaOH,H,O, HEAT b) workup a)excess NaOCH, CH, OH b)1,4-dibromobutane, solvent c)...
5. Show the major organic products after each step of the following reac reactant and products with according to their major functional groups. (6 pts 2 pts for functional groups) total: 2 pts per structure, O HaO+ (catalyst) H30+ (catalyst) CH,OH CH3CH2OH 6. The ether shown below can be prepared by Williamson ether synthesis. (a) Show the structures of the starting materials (alcohol and alkyl halide). (4 pts) (b) Show the complete arrow pushing mechanism that accounts for the formation...