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- 7:21 PM Thu Jul 7 2req 2req ts 2req pts 2req 1 pts 2req [Review Topics] Provide an IUPAC name for the structure shown. ball & stick-labels (Do not use stereochemical terms in you name.) Submit Answer Retry Entire Group 9 more group attempts remaining [References] 29%b Search results for write complet * Illinois State University : CHE 22 X > aromatic nitration assignment.p x A reggienet.illinoisstate.edu/access/content/attachment/ale286d3-b539-436a-9dae-4501422658c6/Assignments/97c80ba1-8f18-42f9-bfad-7694cfc0. E U4SD.Org Imported From IE M TalentEd 4 News & Announce. * U4SD Intranet New Tab TAC O Zoom O EAC ТАС O JunpRope W Illinois REALTORS®. >> aromatic nitration assignment.pdf 1 / 2 + 100% ОН KMNO4 H3C- CH3 H,SO4, H2O 1 С. H OH H,PO, D. Mc 4 O v i 1:11 ТАСthe Lewis acid and Lewis base and wheather they are Bronsted acids and Bronsted bases A. Where are the corved arrow mechanisms locate? In each step, indicate B. What is the number of transition states and the number of intermediate in the mechanism C. What are all of the reasonable resonance contributors. = !01: CH3OH heat D :0 CH3
- (a) The relative neutralizing power of CaCO3 is 100%; (b) Liming material with lower molecular weight compared to that of CaCO3 have higher relative neutralizing power. * A if a is correct B if b is correct C if both statements are correct D if neither statement a nor b are truekindly answer 14 and 15. thank you.1. Draw the structure of the major products of the following reactions HO- (1) DMSO, (COCI)2 (2) EtgN H,CrO, H. (1) KMNO,, HO", A OH (2) H,O*
- Pyridine exhibits a UV transition of the type n at 270 nm. In this transition, one of the unshared electrons on nitrogen is promoted from a nonbonding MO to a (antibonding) MO. What is the effect on this UV peak if pyridine is protonated?Arrange the following compounds in increasing reactivity towards E*. CI Select one: O a. O b. O c. d. IV, I, II, III I, IV, III, II IV, I, III, || II, III, I, IV | OCOCH 3 NH₂ II OH ||| CBr3 IVa) b) c) d) e) 1) BH3/THF 2) H₂O2 NaOH (aq) cold Cl₂, H₂O HBr CH3CH₂OOCH₂CH3 1. Hg(OAc)2, H₂O 2. NaBH4 o 1) 03 (-78 °C) 2) (CH3)S H₂ Lindlar catalyst
- ... Dw.com/ilrn/takeAssignment/takeCovalentActivity.do?locator=Dassignment-take Open Vellum Course Home [Review Topics] [References] 1. H2SO4 Br H20 HO, NaBr + 2. H3C-O H3C-0-Li d = El Elimination f= SN1 Nucleophilic substitution a = Proton transfer e = E2 Elimination g= Sn2 Nucleophilic substitution b = Lewis acid/base c= Electrophilic addition The rections above involve synthesis or reactions of alcohols and ethers. Identify the mechanism by which they proceed from among the mechanisms listed. Use the letters a g fc 1. 2.Give the major organic product(s) of the following. Include stereochemistry when applicable. 1) Nal Br a) 2) NaCN, acetone 1) NaOC(CH3)3, heat d Br 2) BH₂ THF; 3) H,O,, NaOH(aq) b) c) d) c) 2) KOC(CH3)3, heat Copyright University of California Merced 2022 Br 1) NaOH, heat 2) MCPBA 1) KOC(CH3)3, heat 2) H3O+The following reduction can be carried out with which reagent(s)? Select all that apply O A. Zn(Hg), HCI B. 1) NABH4 (excess); then 2) H20, H* O C. H2NNH2, KOH OD. 1) LIAIH4 (excess); then 2) H20, H* O E. 1) HSCH2CH2SH, H*; then 2) Raney Ni (H2) OF. None of these choices