Homework Answers
Option A is the correct option. Water in presence of sulphuric acid we will get Cis diol. B and E will give brominated and chlorinated product respectively. C is having only water which will not react. D is ozone will give us two aldehyde products.
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what would be the reagent?
Part 7 out of 8 Choose the most appropriate reagent(s) for...
Choose the most appropriate reagent(s) for the conversion of the amide to the amine target molecule....
Choose the most appropriate reagent(s) for the conversion of the amide to the amine target molecule. SOCI2 Ph OH Ph CI HN Ph N reagent(s) I- I- A H2, Pd B NaBH4, CH3OH © NaNH2, NHz 1. LiAIH4 2. H*, H20 E NH2NH2, KOH
Choose the most appropriate reagent(s) for the conversion of 2-methyl-1-propanol to 2-methyl-1-tosyloxypropane. CH3 -CH3 reagent(s) I...
Choose the most appropriate reagent(s) for the conversion of 2-methyl-1-propanol to 2-methyl-1-tosyloxypropane. CH3 -CH3 reagent(s) I A 101, Et @ 1,80, H20 C SO3, HCI OSO E TSOH, CH,OH Next part
Part 9 out of 11 6 Choose the most appropriate reagent(s) for the conversion of 1-butanol...
Part 9 out of 11 6 Choose the most appropriate reagent(s) for the conversion of 1-butanol to butanal. PCC CH2Cl2 points COH Cl2 FeCl3 OH reagent(s) Trayers) points A NaOH,H,O, heat B PCC, CH.CH C 1.0 ) LAIH, diethyl ether 2. S(CH) e Na Cr»0», H,804, H,0 13 Design a synthesis of 2-cyclohexenone from 2-methylcyclopentanone. points Part 1: Choose the best option for the precursor to the target molecule. i i Part 2 out of 10 Choose the best option...
Choose the most appropriate reagent(s) for the conversion of 2-methyl-1-propanol to 2-methyl-1-tosyloxypropane. CH3 OTs reagent(s) OH...
Choose the most appropriate reagent(s) for the conversion of 2-methyl-1-propanol to 2-methyl-1-tosyloxypropane. CH3 OTs reagent(s) OH TsCl, Et N sOj, HCI 0 SO, TsOH, CH3OH
Part 5 out of 6 Choose the most appropriate reagent(s) for the second step of the...
Part 5 out of 6 Choose the most appropriate reagent(s) for the second step of the synthesis. H-= H 1. NaNH2 2. CH CH Br reagent(s) A HBr, H,0 ® (CH3),COK (C) NaOH, HẠO 1. B.H 2. HẠO, NaOH H.SO . Hg50, H,0
Part 7 out of 8 Choose the most appropriate reagent(s) for the third step of the...
Part 7 out of 8 Choose the most appropriate reagent(s) for the third step of the synthesis. Br Br2 Br 2 equivalents NaNH2 reagent(s) H3C-E H- А 1. NaNH2 2. CHI B) 1. NaOH C CH31 2. CH3 D NaNH2 E Na, NH3 Check my work
What reagent(s) would be required to accomplish the transformation shown? Please show all steps. What reagent(s)...
What reagent(s) would be required to accomplish the transformation
shown? Please show all steps.
What reagent(s) would be required to accomplish the transformation shown? HA 60 SES -các-CH, C-CHE O 1 . H2, PL H2, Lindlar's catalyst Na, liq. NH3, then H20
Choose the most appropriate reagent(s) for the conversion of (R)-3-bromo-2-methylpentane to (S)-3- azido-2-methylpentane. TsCI pyridine HOH...
Choose the most appropriate reagent(s) for the conversion of (R)-3-bromo-2-methylpentane to (S)-3- azido-2-methylpentane. TsCI pyridine HOH OTS NaBr, acetone reagent(s) N3 A NaN3, CH3S(O)CH; B HN NaNH D NH2NH2 NH
2. Provide the major products from the following reactions. Starting Material Reagent(s) Product? Br2 Place appropri...
2. Provide the major products from the following reactions. Starting Material Reagent(s) Product? Br2 Place appropriate groups H, Br CH, on scaffold) HCI Place appropriate groups (H, Br, CH, on scaffold) CH Brz/H20 Place appropriate groups H, Br CHs on scaffold] 1) O3 2) Zn/HOÁC LICH H2, Pd/C CH₂ 1. BH3 2. H2O2, NaOH(aq) CH2 hot KMnO4 in H2O - CH₂ CH3CO3H Product from above H30+, H2O
Give the missing reagent(s). Due 11/22/19 Give the missing reagent(s). CH3 Пон CH3 ОН CH3 он...
Give the missing reagent(s).
Due 11/22/19 Give the missing reagent(s). CH3 Пон CH3 ОН CH3 он он CH3 пон lot Matching: ACH, инно он CH3 пон "HOH Matching: H2SO4, H20 1) BH3.THF 2) H2O2, OH-1 C2 1) Br2, H2O 2) NaH KMnO4 Cold, Dilute,Basic HCl 1) Hg(OAc)2, H2O 2) NaBH4, OH! H2O, H2SO4 mCPBA 1) mCPBA 2) H:07 H2 1) OsO4 2) NaHSO3 (1) O₃ 2) (CH3)2S Na, Liquid NH; | 1) mCPBA 2) H2O, OH"! Lindlar's Catalyst
Choose the most appropriate reagent(s) for the conversion of the amide to the amine target molecule. SOCI2 Ph OH Ph CI HN Ph N reagent(s) I- I- A H2, Pd B NaBH4, CH3OH © NaNH2, NHz 1. LiAIH4 2. H*, H20 E NH2NH2, KOH
Choose the most appropriate reagent(s) for the conversion of 2-methyl-1-propanol to 2-methyl-1-tosyloxypropane. CH3 -CH3 reagent(s) I A 101, Et @ 1,80, H20 C SO3, HCI OSO E TSOH, CH,OH Next part
Part 9 out of 11 6 Choose the most appropriate reagent(s) for the conversion of 1-butanol to butanal. PCC CH2Cl2 points COH Cl2 FeCl3 OH reagent(s) Trayers) points A NaOH,H,O, heat B PCC, CH.CH C 1.0 ) LAIH, diethyl ether 2. S(CH) e Na Cr»0», H,804, H,0 13 Design a synthesis of 2-cyclohexenone from 2-methylcyclopentanone. points Part 1: Choose the best option for the precursor to the target molecule. i i Part 2 out of 10 Choose the best option...
Choose the most appropriate reagent(s) for the conversion of 2-methyl-1-propanol to 2-methyl-1-tosyloxypropane. CH3 OTs reagent(s) OH TsCl, Et N sOj, HCI 0 SO, TsOH, CH3OH
Part 5 out of 6 Choose the most appropriate reagent(s) for the second step of the synthesis. H-= H 1. NaNH2 2. CH CH Br reagent(s) A HBr, H,0 ® (CH3),COK (C) NaOH, HẠO 1. B.H 2. HẠO, NaOH H.SO . Hg50, H,0
Part 7 out of 8 Choose the most appropriate reagent(s) for the third step of the synthesis. Br Br2 Br 2 equivalents NaNH2 reagent(s) H3C-E H- А 1. NaNH2 2. CHI B) 1. NaOH C CH31 2. CH3 D NaNH2 E Na, NH3 Check my work
What reagent(s) would be required to accomplish the transformation
shown? Please show all steps.
What reagent(s) would be required to accomplish the transformation shown? HA 60 SES -các-CH, C-CHE O 1 . H2, PL H2, Lindlar's catalyst Na, liq. NH3, then H20
Choose the most appropriate reagent(s) for the conversion of (R)-3-bromo-2-methylpentane to (S)-3- azido-2-methylpentane. TsCI pyridine HOH OTS NaBr, acetone reagent(s) N3 A NaN3, CH3S(O)CH; B HN NaNH D NH2NH2 NH
2. Provide the major products from the following reactions. Starting Material Reagent(s) Product? Br2 Place appropriate groups H, Br CH, on scaffold) HCI Place appropriate groups (H, Br, CH, on scaffold) CH Brz/H20 Place appropriate groups H, Br CHs on scaffold] 1) O3 2) Zn/HOÁC LICH H2, Pd/C CH₂ 1. BH3 2. H2O2, NaOH(aq) CH2 hot KMnO4 in H2O - CH₂ CH3CO3H Product from above H30+, H2O
Give the missing reagent(s).
Due 11/22/19 Give the missing reagent(s). CH3 Пон CH3 ОН CH3 он он CH3 пон lot Matching: ACH, инно он CH3 пон "HOH Matching: H2SO4, H20 1) BH3.THF 2) H2O2, OH-1 C2 1) Br2, H2O 2) NaH KMnO4 Cold, Dilute,Basic HCl 1) Hg(OAc)2, H2O 2) NaBH4, OH! H2O, H2SO4 mCPBA 1) mCPBA 2) H:07 H2 1) OsO4 2) NaHSO3 (1) O₃ 2) (CH3)2S Na, Liquid NH; | 1) mCPBA 2) H2O, OH"! Lindlar's Catalyst
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