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- What series of reagents will accomplish this transformation? ch9_d5_q4.pdf O 1. BH3-THF 2. H2O2, NaOH 3. H₂SO4, heat 4. mCPBA 5. H3O+ O 1. Hg(OAc)2, H₂O 2. NaBH4 3. H₂SO4, heat 4. mCPBA 5. H3O+ O 1. BH3-THF 2. H2O2, NaOH 3. H₂SO4, heat 4. OSO4, NMO O 1. Hg(OAc)2, H₂O 2. NaBH4 3. H₂SO4, heat 4. OsO4, NMOContent 54°F Clear * X app.101edu.co Draw the major product of the substitution reaction shown below. Ignore any inorganic byproducts. F1 Aktiv Chemistry. @ 2 CH3CO2H Draw SN1 Product F2 # 3 DII X OSN2/SN1 Reactions Fl: X G Which alkyl bromide i X F3 $ ▬ F4 % 5 J F5 A 6 Question 8 of 22 â 6 F6 & G whats a stro 7 Please select a c F7 O PrtScn 8Fill in the missing products below. 1) Hg(OAc)2, EtOH 2) NaBH4 Excess HI A B Heat RCO3H 1) H-CEC: Na D 1) NaSEt 2) H3O+ 2) H₂O+ → E HBr → F
- 3. Fill in the boxes to propose syntheses for the following molecules. OHChoose reagents to convert 2-cyclohexenone to the following compounds. Syntheses may require several steps. Use letters from the table to list reagents in the order used (first at the left). i 1. Li(CH2=CH)2Cu Reagents a 1. Li(CH3)2Cu 2. H3O+ e 1. Li(C6H5)2Cu 2. H3O+ b 1. NaBH4 f CH2l2/Zn(Cu) / ether j 2. H3O+ C NH3 / KOH g 1. CH3MgBr/dry ether k 2 H3O+ d H2NNH2/KOH h HN(CH3)2 HO CH3 a) b) OH N(CH3)2 2. H3O+ (C6H5)3P+-CH2 H₂ over Pd/C KMnO4/H3O+6. Provide the missing reagent(s) that gives the desired product in high yield. POMOL 129 129 16m2 sn RCH₂CH₂ ? CH₂CH₂R 20112⁰ D">OH H₂CO-D H H A) NaOCH3 B) 1. TsCl/Base; 2. NaOCH3 C) 1. NaH; 2. CH3I D) 1. CH3COCI/Base; 2. NaOCH3
- #5please provide answer with details thank youSelect the appropriate reagent from the reagent bank to accomplish each step in the reactions below. Reaction 1: Reaction 2: Reaction 3: Reaction 4: G Reaction 1 НО. Reaction 2 lo Reaction 3 iOH OH Reaction 4 CN NH₂ ? ? . ? ? НО. loh OH lot NH₂ HO 1) BH3THF 2) H3O+ A HNEt₂ E 1) Et₂CuLi 2) H₂O I mCPBA M Reagent Bank ta NaH B HCI H₂O F HNEt₂ Trace H+ J SOCI₂ N CH3OH H* C 1) EtMgBr 2) H₂O G H₂C=PPh3 K H₂NEt Trace H* O 1) LIAIH4 2) H₂O D 38 НО. H* H -OH H* L DCC OH P
- Alcohols are important for organic synthesis, especially in situations involving alkenes. The alcohol might be the desired product, or the OH group might be transformed into another functional group via halogenation, oxidation, or perhaps conversion to a sulfonic ester derivative. Formation of an alcohol from an alkene is particularly powerful because conditions can be chosen to produce either the Markovnikov or non-Markovnikov product from an unsymmetrical alkene. Using your reaction roadmap as a guide, show how to convert 4-methyl-1-pentene into 5-methylhexanenitrile. You must use 4-methyl-1-pentene and sodium cyanide as the source of all carbon atoms in the target molecule. Show all reagents needed and all molecules synthesized along the way.Choose reagents to convert 2-cyclohexenone to the following compounds.What starting material with these reagents will result in 1. NANH2 2. CH3CH2BR 3. H2, Lindlar's cat.