You are told synthesize cumene starting from benzene and any other reagents. You find 1- chloropropane...
Provide the reaction for chlorination of benzene using electrophilic aromatic substitution, it's complete mechanism including formation of "super" electrophile, and a completely labeled reaction coordinate energy diagram. 1.
please help in all sections asap!! Provide the reagents necessary to carry out the following conversion. NO Br Choose the correct reagents for step 1. fuming H2SO4 Br2/ FeBr3 HNO3/ H2SO4 CH3Br / FeBr3 Choose the correct reagents for step 2 HNO3/ H2SO4 CH3Br/ FeBr3 fuming H2SO4 Br2/ FeBry Which one of the following substituents will direct the incoming group to the meta position during electrophilic aromatic substitution? -NO2 -CEN -CCl -COOH all of these O O Identify the electrophile...
Please help with questions 1-5. I have attached the additional lab information pages for help if you are unclear on anything please review those. We were unable to transcribe this imageEAS 97 5. Calculate the theoretical yiel te the theoretical yield of iodinated salicylamide (product) ass Todination reaction. (Show your calculations.) mide (product) assuming a mono- le, your starting material, is shown in Figure 4. ces in the functional group region of the spectrum IR spectrum of salicylamide, your starting...
QUESTIONS 1. What is the purpose of the sulfuric acid (yes, it's a catalyst, but why is it a catalyst? What is it doing that makes the reaction possible? Would the reaction just go slower without it, or would the reaction not go at all? Why?) 2. If isobutyl alcohol (2 methyl propanol) is used instead of tert butyl alcohol, a mixture of products is obtained. One the products is the same as the product obtained with the tert butyl...
1.) (9 points) Give structures for the following compounds: a) meta-phenylphenol b) 6-benzyl-3-heptanol e) ortho-sec-butyltoluene 2.) (9 points) Name the following compounds: 3.) (8 points) Label the following molecules as aromatic, anti-aromatic, or non-aromatic. For the ones th aren't aromatic, explain why they are either non-aromatic or anti-aromatic. 0.8 4.) (11 points) For the following electrophilic aromatic substitution reaction: Вт, FeBr; a) Which product is the major one? b) Draw a complete mechanism for the formation of the major product...
please help in all sections asap!! Provide the reagents necessary to carry out the following conversion. ОСН Br Br NO2 Choose the correct reagents for step 1 fuming H2SO4 HNO3/H2S04 excess Br2/ FeBr3 dilute H2SO4 O Cl2/FeCly O CH3ONA Choose the correct reagents for step 2. Cl2/ FeCl3 HNO3/H2SO4 CH3ONA fuming H2SO4 excess Br2/ FeBr3 dilute H2SO4 Choose the correct reagents for step 3 CH3ONA HNO3/ H2SO4 O excess Br2/ FeBr3 Odilute H2S04 fuming H2SO C2/ FeCl Choose the correct...
if anyone can check these answers for me and tell me which are right or wrong id appreciate it 0. How can p-aminobenzoic acid (a sunscreen) be synthesized from benzene? (Note that sometimes more than one isomer will be obtained, which is fine as long as the desired isomer is one of the major products.) several steps HOOC 4. Sn, HC 4.KMnO. .KMnO 4.Sn, HC 3.KMnO 3. CHCI, AİCİ, 3. Sn, HC . HNO, H SO 2. HNO,, H:SO4 1,...
Can you help me identify reagent (i), Compound 8 and Compound 12 in the reaction scheme? You have laboratory data on all the compounds in the synthesis, however the amount of data available to you varies. Some have the entirety of the spectral data, others have as little as the elemental analysis. Use the laboratory data to help you discover which reaction has been performed. The lab data for Compound 8 and 12 is as follows: You can use any...