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Please answer parts 4-6: Br2 (excess), H2, Pt catalyst, and NaNH2, NH3 (liq.)
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- Choose the best reagents from the list provided below for carrying out the following conversion. Match the reagent with the step number. HCl (aq), Zn(Hg) KMnO4, H3O+ CH3Cl, AlCl3 HNO3, H2SO4 Cl2, FeCl3 fuming sulfuric acidHi there, can someone please help me solve for the products of the following reaction? Please make sure to clarify all steps taken to go about solving for the products and explain various terms and rules that should be known or correlate with the question. I'm using these questions to study for our final exam and need some extra clarification on rules and steps. Thank you very much in advance!CH₂ + Using the reagents below, list in order (by letter, no period) those necessary to prepare 2-butyne from acetylene. Note: Not all spaces provided may be needed. Type "na" in any space where you have no reagent. a. Br₂, heat, light b. Na, (-H₂) c. Nal(SN2) d. NH4NO3 e. 1) NaNH2, liq. NH3, 2) CH3Br f. (CH3)3COK, (CH3)3COH, heat g. NaOEt, EtOH, heat Step #1 Step #2 Step #3
- My question is asked on the picture that I am uploading, I sincerely hope Bartleby can help me more than Chegg ever did! Thank you! I need help finding the major products and minor products of the written reaction!You continue to impress people at the chemical company and they give you a special assignment. Compound C needs to be converted to Compound D and you are tasked to come up with a route for this. Design a route to take C to D, outlining the reagents you would use for each step. You should use only reactions that have been covered in the Oranic chem 1 course, and it will take more than one stepfrom the list of reagents select those that carry out the transformation above the list.please make sure the corrosponding letters are in the correct order for the reaction starting on the left.i.e. cd = 1. LiAlH4 then H3O+, 2. H2, Pd/C
- (a) Give the names of reagents and conditions for each of the reactions I and IIUsing your knowledge of general chemistry and organic chemistry, answer the following questions: Predict the relative acidities within each of the following groups, then identify the conjugate bases, and finally predict their relative leaving group abilities HClO3 and HClO2 PH3 and H2S [NH4]+ and [H3O]+ Explain why the trifluoromethane sulfonate (TfO-) ion is a better leaving group than the methanesulfonate (MsO-) ion.Hi there, can someone please help me solve this problem? Please make sure to clarify all steps taken to go about solving for the products and explain various terms and rules that should be known or correlate with the question. I'm using these questions to study for our final exam and need some extra clarification on rules and steps. Thank you very much in advance! You must use enolate anion chemistry as part of a synthesis of the following molecules.
- Please answer questions 4, 5 and 6 on the attached sheet. Please provide the major and any minor products for the SN1 and E1 reactions and explain how they were calculated. Thank you.Explain why the following reaction is not a good way to prepare 1-phenylpentane: benzene + 1-chloropentane + AlCl3 → 1-phenylpentane In your scratch work, give the full, curved-arrow mechanistic explanation of what would happen, and indicate what would likely be your main product or products.Can someone explain 2E the question is asking and this is what my professor said but I am lost as heck now please help here is the question: The last person said it was TsCl and lithium aluminum hydride so would E have two answers. I am just really confused now. Q: Provide the reagents needed to carry out the reactions below (or the product obtained). If two steps are needed, clearly indicate 1. (reagent A); 2. (reagent B). If separate steps are not indicated, I will assume you mean that all reagents are introduced together.