5. MULTISTEP SYNTHESIS: Provide a synthesis for the formation of the following compounds using benzene as a starting material and any other reagents you need. Use numbers in your answer for the proper sequence of reagents that you would use. Note: you are only being asked to provide the reagents to prepare each of these compounds from benzene. a. -Br

5. MULTISTEP SYNTHESIS: Provide a synthesis for the formation of the following compounds using benzene as a starting material and any other reagents you need. Use numbers in your answer for the proper sequence of reagents that you would use. Note: you are only being asked to provide the reagents to prepare each of these compounds from benzene. a. -Br

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter19: Eas: Electrophilic Aromatic Substitution

Section: Chapter Questions

Problem 7E: When toluene is treated with sulfuric and nitric acids under special conditions, three nitro (NO2)...

See similar textbooks

Similar questions

Show how you would synthesize each compound from benzene, toluene, or phenol using the following reactions: Reactions 1. Halogenation 2. Nitration 3. Sulfonation 4. Friedel-Crafts acylation 5. Friedel-Crafts alkylation 6. Oxidation of methyl group 7. Reduction of nitro group • Choose the starting material from the drop-down list • Enter the number(s) of the desired reactions in the order that you wish to use them without commas between • If a reaction is used more than once, enter its number each time you wish to use it Compound 1: 5-chloro-2-methylbenzenesulfonic acid Starting material: toluene Reaction(s): 31 Compound 2: m-bromobenzoic acid Starting material: [benzene Reaction(s): Submit Answer Try Another Version 1 item attempt remaining
6. Provide a synthesis for the following molecule. Br
8. Provide a synthesis for the following molecules.
3. Depict a synthesis for the following product starting from benzene and any other organic or inorganic materia
Write the structural formula of the organic product for the given reaction between an alkyne and an alkyl halide. The alkyne group is shown and should be entered as "CC" without the triple bond. Enter C before associated H atoms (e.g., CH3CH2CH2OCHCHCH2). CH3CH2CH2CCH 1. NaNH, 2. CH3CH2Br
Propose a synthesis of octane starting from 1-pentyne. Specify the reagents you would use to carry it out. If two or more routes to the same product are possible, show only one of them. (Specify reagents using letters from the table, the first reagent on the left. Example: ab) a.1. BH3 2. CH3COOH Reagents available c. OsO4, H₂O2 The reagents are : d.1. Hg(OAc)2, H₂O NaBH4 2. b. H,O, H,SO4, HgSO e.1. NaNH, / NH 2. CH3 CH₂ CH₂ Br f. H₂/ Lindlar catalyst g. H₂ / Ni h. 2 mol Na / NH3 (1)
2. Synthesis questions a. N. from ethyl bromide (the methyl groups in the product have to come from ethyl bromide) b. C. d. N from (all 6 carbons in the product have to come from the indicated starting material C(CH3)3 from F CON(Et)2 Br from all the aromatic carbons in the product must come from the starting material but you can use any other reagents all the aromatic carbons in the product must come from the starting material but you can use any other reagents
Provide the major organic product for the 1. LilH 4 2.нсін, о Provide the major organic product of the following reaction. following reaction. ?. 6. Provide the major organic product for the following reaction. HO Br OH NH - Br 1. LIAIH4 2. HC1, H₂O 7. Provide the major organic product of the following reaction. concentrated KMnO4 reflux
Write the structural formula of the organic product for the given reaction between an alkyne and an alkyl halide. The alkyne group is shown and should be entered as "CC" without the triple bond. Enter CC before associated HH atoms (e.g., CH3CH2CH2OCHCHCH3). 1.NaNH2 CH3CH2CCH------> 2. CH3CH2b2
2. Check the reaction given below. Benzoic acid is synthesized from benzene. Suggest a synthetic route from benzene to benzoic acid with the reactions you learn in electrophillic aromatc substitution reactions. PS: This is not a one step reaction !!! .COOH 3. You all know the carbonyl structure. It is carbon atom double bonded to the oxygen atom. a. Draw the dipol moment of the carbonyl structure. b. Here are two different carbonyl bearing molecules. With the knowledge you learned so far explain which one is more stable and why? CH3 H3C H3C b. а. 4. Is it possible to achieve this reaction directly? Explain your reasons. *CH3
Provide the major organic product of the following reaction. 1. Т.С, ругidine 2. NaBr
1. Nitration of pyridine occurs primarily at the 3-position as shown in the reaction below. Explain why nitration at this position is favored over nitration at the 2 or 4 position. Use structures to support your answer. Note that the numbering of the ring begins with the nitrogen as position 1. HNO3 H₂SO4 `N .NO₂