Match the reagent to the specified outcome ??? 3-methylbut-1-ene 1. BHz: THE 2. NaOH, H2O 1....
Match the reagent to the specified outcome ??? 3-methylbut-1-ene 1. BHz: THE 2. NaOH, H2O 1. Hg(OAc)2, H20 2. NaBH4 C.Not possible in one step D. H2SO4, H20 3-methylbutan-2-ol
Using 3 different sets of reagents on 3-methylbut-1-ene, it s possible to obtain 3 different alcohols. Specify which reagent will produce the indicated alcohol from 3-methylbut-1-ene QUESTION 1 Match the reagent to the specified outcome | ??? 3-methylbut-1-ene A. Not possible in one step 니 H₂SO4, Ho 3-methylbutan-2-ol 1. Hg(OAc)2, H2O) 2. NaBH4 \ 1. BH3: THE 3-methylbutan-1-ol 2. NaOH, H2O, HO 2-methylbutan-2-ol HOT 2-methylbutan-1-ol
Specific which reagent will produce the indicated alcohol from 3-methylbut-1-ene. QUESTION 1 10 points Save Answer Match the reagent to the specified outcome ??? 3-methylbut-1-ene OH 1. BH; THF 2. NaOH, H2O2 . Not possible in one step 3-methylbutan-2-ol H2SO4, H2O Click Save and Submit to save and submit. Click Save All Answers to save all answers. Save All Answers Save All Answers Save and Submit Save and Submit 3-methylbutan-2-ol H2SO4, H20 OH 1. Hg(OAc)2, H20 3-methylbutan-1-ol 2. NaBH4 HO...
NaBH4 CC Hg(OAC)2 H20, THE NaOH 1. Hg(O2CCF3)2, 'ProH 2. NaBH4, NaOH 1. BHz •THF 2. H2O2, HOⓇ R-OH + Nax — NaCN DMSO TSCI pyridine ОН MSCI pyridine NasMe DMSO cat. HA MeOH + g. Arrange in the Increasing acidity order HẠO ROH RC=CH HA NHA RH. cold KMnO4, HOor 1. Os04 2. NaHSO3 MICH3 1. mCPBA 2. H+, CH3OH, H2O 1. mCPBA 2. NaOCH3, H20 H2O / H+ Hg(OAC)2 H2O, THE NaBH4 NaOH 1. BH3 THF 2. HaO2...
match the right reagent 3 OH + enantiomer + enantiomer 5 CO A.) PBrs B.) NBS, hv C.) D.) NaOH E.) NaNH2 F.) Br2 G.) HCI H.) Cl2, H2O 1.) HBO J.) H2 (1 eq), Pt K.) Na, NH3 L.) H2SO4, H20 M.)1. Hg(OAC)2 0.) N.) 1. mCPBA 2. H+, H2O 2. NaBH4 P.) 1. BH3 2. H2O2, NaOH 3 OH + enantiomer + enantiomer 6 CO A.) PBrs B.) NBS, hv C.) D.) NaOH E.) NaNH2 F.) Br2 G.)...
match the right reagent ОН 7 8 ОН г. . . . . . . + enantiomer A.) PBrs B.) NBS, hv C.) D.) NaOH E.) NaNH2 F.) Br2 G.) HCI H.) Cl2, H2O 1.) HBO J.) H2 (1 eq), Pt K.) Na, NH3 L.) H2SO4, H20 M.)1. Hg(OAC)2 0.) N.) 1. mCPBA 2. H+, H2O 2. NaBH4 P.) 1. BH3 2. H2O2, NaOH
which route from the choices listed below is the best procedure for converting 3-phenylbut-1-ene to 3-phenylbutan-1-ol Which route from the choices listed below is the best procedure for converting 3-Phenylbut-1-ene to 3-Phenylbutan-1-ol? -OH a. i. HCl; ii. NaOH b.i. Hg(OAc)2; ii. NaBH4 с. Н30* d. i. BH3; ii. H202, NaOH, H20 e. NaOH, A f. H202
please match 1-4 with A-D. thank you. Q14.7 Homework Unanswered Match the reagent needed to accomplish the following transformations. Dilute H2SO4 1) а 1) Hg(OAc)2, Н2о b) ОН 2) NaBH4, NaOН, Н2О ОН 2) Brz, Hа0 НО 1) ВНз-ТHF d 3 2) HzО2, H2о Br 4 ОН Premise Response Drag and drop to match 1 1) A Reagent a 2 2) Reagent d 3) Reagent C 4) Reagent b D 3
Which route from the choices listed below is the best procedure for converting 3-Phenylbut-1-ene to 3-Phenylbutan-1-ol? OH a. NaOHA b. i. HCl; ii. NaOH CH202 dH30* e.i. BH3; 11. H2O2, NaOH, H20 f. i. Hg(OAc); ii. NaBH4
Starting from 3-methylhex-1-ene as the substrate at the center of your page, draw a reaction map showing the regiochemical and stereochemical outcome or outcomes for each of the following series of reagents. Name each of your products, including stereochemical designations for any chirality centers that are generated.**Pay attention to the possibility of rearrangement when your mechanism produces a carbocation. A. H2SO4, H2OB. 1. Hg(OAc)2, H2O; 2. NaBH4C. 1. BH3•THF; 2. H2O2, NaOHD. Br2, CCl4E. Br2, H2OF. HBrG. HBr, ROORH. 1. O3; 2. DMSI. H2, Pt