Current Attempt in Progress * Your answer is incorrect. Identify the synthesis that will achieve the following transformation. CI ? ● O AICI, HNO₂ H₂SO4 HNO, H₂SO4 HNO, H₂SO Bry Fe Bry 1) Fe, H₂0¹ 2) NaOH Br₂ Fe Bry Br Fe Bry Br CuCl Bry Fe Bry 1) Fe, H₂0+ 2) NaOH NaNO₂ HCI NaNO₂ HCI CuCl CuCl A
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- steps and reagents 1. PhMgBr, THF 2. H2O, HCl 3. H2SO4 4. Br2, H2O Please give a detailed mechanismMatch the questions with the correct descriptions below: Sn2, E2 E1cb Sn1, E1 (anti) E2, E1cb Sn1, E1 2 steps poor leaving group 2 carbons removed from a carbonyl group carbanion intermediate 3°>allylic, benzylic>2°>1°>CH₃ carbocation intermediate Ist order reaction (r=k[RX]) H-X anti no intermediate 2nd order reaction (r=k[RX][Nu]) polar aprotic solventselect the most appropriate reagent(s) to effect the change. K2Cr2O7, H+ H2, Pd 1. Disiamylborane, 2. HO–, H2O, H2O2 NaOCl H2SO4, HgSO4
- Show a complete mechanism for the meta-bromination of nitrobenzene (PhNO2) using Br2/FeBr3 to give meta-bromonitrobenzene. Use resonance forms to explain why nitrobenzene directs meta.Possible route of synthesis 1)Br2, H2O 2) H2SO4,H2OPropose a plausible mechanism for each of the reactions below with clear arrow pushing please answer fast i give upvote
- Choose the best reagents from the list provided below for carrying out the following conversion. Match the reagent with the step number. HCl (aq), Zn(Hg) KMnO4, H3O+ CH3Cl, AlCl3 HNO3, H2SO4 Cl2, FeCl3 fuming sulfuric acidPlease help me with the mechanism for what is described below: 1. Draw a mechanism for the reaction dscribed: The Wittig Reaction Reactants: NaOH, (4-picolyl)triphenylphosphonium chloride, dichloromethane, 4-pyridinecarboxaldehyde (also known as isonicotinaldehyde), HCl, Na2CO3 Final product: trans-4,4'-bpeShow the mechanism of the following reactions and show their products.1. CH3CH2OH+ HBr --> ?2. CH3CH = CH2 + HCl --> ?3. C6H6 + HNO3 --> ?4. CH3CH2OH + H2SO4 (concentrated) --> ?5. CH3O- + CH3Br --> ?
- Need your help for this: Show the reaction mechanism for the formation of a. RCONH2 from the reaction of RCOOR' with NH3 b. RCOOR" from the reaction of RCOOR' with R"OH in acidic mediumHelp ASAP Illustrate the resonance effect of the methoxy group -OCH3, on the structure of the benzene ring. Do this by writing all the possible resonance forms for methoxybenzene, including the hybrid. Based on your structures, explain how the presence of the -OCH3 group affects: (i) the reactivity of the benzene ring towards electrophilic attack; (ii) the orientation or point of attack of an incoming electrophilic reagent on the benzene ring.Which reactions will proceed faster in a polar, aprotic solvent? (CH3)2CHCH2I+Na+N3−(CH3)2CHCH2I+Na+N3− (CH3)3CBr+HSCH2CH3(CH3)3CBr+HSCH2CH3 CH3CH2CH2Br+Na+CN−CH3CH2CH2Br+Na+CN− (CH3)2CHOSO2CH3+HOCH(CH3)2