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Develop a synthesis for the following molecule using only the indicated materials as sources for the carbon atoms that appear in the final product. As a hint, you will need to draw upon several reactions from earlier chapters to come up with a successful solution, and you may have to use some of the carbon sources more than one time. Also assume that
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- Starting with benzene and using any other reagents of your choice, design a synthesis for the following compound: Br XX O₂N The target molecule above can be prepared by treating benzene with some reagent or combination of the reagents listed below. Give the necessary reagents in the correct order, as a string of letters (without spaces or punctuation, such as "EBF"). If there is more than one correct solution, provide just one answer. A HNO3, H₂SO4 D Fuming H₂SO4 B E Br2, AlBr3 Dilute H₂SO4 C BrMg F MgBr axxa. AICI 3arrow_forwardStarting from acetylene and alkyl halides not longer than 4 carbon atoms, show the synthesis of 3-octanol and a ketone. Indicate the reagents in each step. You may use more than one mole of the reactants.arrow_forward10. Propose a multi-step synthesis to prepare para-nitrotoluene from benzene. NOTE: You can just provide the description or name of the reaction, you do not have to provide the actual reagents.arrow_forward
- Show how to synthesize the following product as the major product starting with 2,2-dimethylpropane as the starting material. You may use additional reagents and any number of steps. Be sure to list each step with all reactants/reagents/conditions required. (Do not use hydrogenation reactions). Write the process.arrow_forwardYou are a chemistry company's latest chemistry recruit and your first job is to prepare 2-methylcyclohexanol. The one key starting material you have been given is methylcyclohexane. Draw a scheme to take you from the starting material to the product outlining the reagents you would use for each step as well as the key organic product(s) formed from each step. [Note: You do not need to show mechanisms for any steps]arrow_forwarddo 2,3,4 pleasearrow_forward
- Provide a synthesis for the target molecule shown below, starting with an alkyl halide or alcohol of your choice. In each case, show your retrosynthetic analysis, and then provide a complete synthesis, showing all necessary reagents. { Which of the following syntheses are suitable to prepare the given target molecule (as the major product formed)? Select all that apply. 0 0 0 O 1) TsCl, pyridine OH 2) NaOEt OH -CI 1) TsCl, pyridine 2)1-BuOK NaOH t-BuOK conc. H₂SO4 Pots OH heat t-BuOKarrow_forwardStarting with benzene and using any other reagents of your choice, design a synthesis for the following compound: The target molecule above can be prepared by treating benzene with some reagent or combination of the reagents listed below. Give the necessary reagents in the correct order, as a string of letters (without spaces or punctuation, such as "EBF"). If there is more than one correct solution, provide just one answer. A CH₂CH₂COCI, AICI D (CH3)2CHCI, AICI B HNO3, H₂SO4 E Cl₂, AICI C 1) CH₂CH₂COMgBr 2) H30* F 1) (CH3)₂CHMgBr 2) H₂O¹arrow_forwardComplete the following reaction schemes by choosing the correct product, starting material, and/or reagent from the selection below. Your answer should simply be the number that represents your choice. For example, if you believe that the correct answer is the structure represented by the 3, then enter 3 into the correct answer box. Also, answer any additional questions that might be included with a reaction scheme(s). H₂C 0 1. NaNH, 1. NaNH, 2. CH₂CH₂CH₂Br 2. CH₂CH₂Br OH 1 4 3 2 5 O 6 Naº NH3 (1) 11 OH 7 7 XXXXXXXXX E RUTINE H H₂ Pd/C, CaCO3 8 1. NaNHz 2. CH₂(CH₂)₂CH₂Br 13 MCPBA 12 A B a. What reagent(s) is/are required for reaction A to proceed as drawn? What reagent(s) is/are required for reaction B to proceed as drawn? H₂C 9 H₂ Pd/C 14 -0 CH3 Br 10 1. BH-THF 2. H,O2, HỌ, H,O 15arrow_forward
- Suggest typical reagents needed to convert an alkene into an aldehyde (e.g. B to C). Your answer may be written using either words and/or combinations of appropriately formatted chemical symbols. If more than one step is needed, then this must be indicated as follows: 1) NaCl, 2) H₂O Answer: Check B X² X₂ Stel tipiese re alkeen na 'n a antwoord kan kombinasies simbole. As m soos volg aamarrow_forwardProvide a synthesis for the target molecule shown below, starting with an alkyl halide or alcohol of your choice. In each case, show your retrosynthetic analysis, and then provide a complete synthesis, showing all necessary reagents. Which of the following syntheses are suitable to prepare the given target molecule (as the major product formed)? Select all that apply. O OH 1) TsCl, pyridine 2) NaOEt 1) TsCl, pyridine 2) I-BuOK OH CI NaOH Ra об OH CI t-BuOK conc. H₂SO4 heat CI t-BuOKarrow_forward3) A common practice that organic chemists work on is a process known as retrosynthesis. In this a chemist will take known reactants and devise a synthetic pathway to produce the desired products using reactions that they know. As you proceed through organic chemistry you will be tasked with thinking about this process. How would you make the desired final product starting from the alkyne. It will take a couple of reactions. Please show the reagents necessary. And for your last step please show the arrow pushing. Starting material Br Product Br ...arrow_forward
- Organic ChemistryChemistryISBN:9781305580350Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. FootePublisher:Cengage Learning