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- ollowing is a conjugated d A) ich of the following is A) OCH 3 CHEM 242 Act 2.2 Aromatics Compounds and EAS Reactions 8. Provide a mechanistic and resonance explanation as to why bromination (Br₂/FeBr3) of acetophenone occurs meta compared to bromination of anisole, which occurs para. For simplicity, go ahead and use "Br+" as the electrophile. Draw the mechanism for the reaction and resonance structures of the Substrate before the reaction occurs.What compounds will be a major product of the reaction sequence below (1) Brz, hv (2) Mg/ether он OH (A) (B) (3) (4) dil. H* /H2O OH (C) (D) он Compound C Compound D Compounds A and B Compounds B and D (6)I want clear handwritten solution only....i will up vote
- Don't use AI.A key step in the synthesis of β-vetivone, a major constituent of vetiver, a perennial grass found in tropical and subtropical regions of the world, involved the reaction of compound A and dihalide B with two equivalents of LDA to form C. Draw a stepwise mechanism for this reaction. β-Vetivone contains a spiro ring system—that is, two rings that share a single carbon atom.Propose the reagents in best order for the synthesis of the following compound from benzene. CI A) B) 1) CH3CH2Cl, AlCl3 2) Cl₂, AlCl3 3) CH3COCI, AlCl3 1) CH3CH2Cl, AlCl3 2) CH3COCI, AlCl3 3) Cl₂, AlCl3 D) 1) CH3CH2Cl, AlCl3 2) Fuming H₂SO4 2) Cl₂, AlCl3 3) CH3COCI, AlCl3 4) Dilute H2SO4 E) C) 1) CH3COCI, AlCl3 2) Zn(Hg), HCl, Heat 3) Fuming H2SO4 4) Cl₂, AlCl3 5) Dilute H2SO4 1) CH3COCI, AlCl3 2) Cl₂, AlCl3 3) CH3CH2Cl, AlCl3 4) Zn(Hg), HCl, Heat
- 1) Show how m-toluidine (shown on the right) can be converterd to the following compounds using any neccesary reagents. (You can use a previously synthesized compound to carry on). a) H₂C- b) d) c) H₂C m-toluonitrile m-iodotoluene H₂C. CN m-cresol CHÍNH, OH H₂C.Slow addition of organolithium reagent A to B afforded C, anintermediate in the synthesis of the chapter-opening molecule,resiniferatoxin. Draw a stepwise mechanism for this process.Explain the reactivity and orientation effects observed in eachheterocycle Pyridine is less reactive than benzene in electrophilic aromaticsubstitution and yields 3-substituted products.
- What is the order of decreasing reactivity towards nucleophilic acyl substitution for the carboxylic acid derivatives? (most reactive first) LOCH₂ BOLOLOK BOLNOM) BC-1-OCK, (CHI)CH-1-OCH, H₂C- H₂C- -C-N(CH3)2 H₂C—C -0 C-CH3 A) II, IV, III, I B I, III, IV, II C) II, I, III, IV D I, II, III, IV I II III IVIdentify compounds A – E of the reaction sequence shown in Scheme III, making sure to include stereochemistry as appropriate.a) Identify compound A in Scheme III. b) Identify compound B in Scheme III. c) Identify compound C in Scheme III. d) Identify compound D in Scheme III. e) Identify compound E in Scheme III.Arrange the following compounds in their ease of undergoing an SN2 reaction: a) СНЗСН2СH2-CІ b) (CH3)2CH-Br с) (СH3)3C-CI d) CH3-Br Question 2 Arrange the following compounds in their ease to undergo solvolysis: a) CH3CHBrCH2CH3 b) C6H5CCI(CH3)2 с) (СН3)ЗС-Вr d) CHЗСН2-