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CH, Bre, light CI 1 Brz, AIBr; A B AICI HNO, c CO, HCI; Cuci, AICI3...
Please help with these practices. Which undergoes the fastest electrophilic substitution with Br2 or AlBr3? Which...
Please help with these practices. Which undergoes the fastest
electrophilic substitution with Br2 or AlBr3?
Which substrate undergoes the most rapid electrophilic
substitution with HNO3/H2SO4?
Which reaction sequence results in this?
What is the major product for the reaction?
CH3 Оснз осна осна Br Б) с) d) NO2 осна осна OCH2CH3 OCH2CH3 H2C a) b) c) d) CH3 SO3H NO2 SO3H OCH3 Br OCH3 CI a) SO3 H2SO4 HNO3 H2SO4 Pd(OAC)2 AICI: (HO)2B OCH3 Br2 b) HNO3 H2SO4 SO3 H2SO4...
Draw the product(s) of the following reactions HNO,/H2SO а. Br b. AICI он So/H2SO C. Он...
Draw the product(s) of the following reactions HNO,/H2SO а. Br b. AICI он So/H2SO C. Он Br/FeBr3 d. HNO3/H2SO4 Br e. OCH3 H3CO. f. AICI OCH3 но g. AICI NO3 Bro/FeBr3 h.
Give the product structures throughout the scheme, from A to I. Follow the series of reactions....
Give the product structures throughout the scheme, from A to I.
Follow the series of reactions.
Show product of this nucleophilic aromatic substitution
reaction.
Provide how a Diels Alder reaction would perform on this
compound.
Thanks so much
1) (27 points) Give the structures of compounds A through I in the following series of reactions CHE Brz, light CI Brz, AIBry AICI CO, HCI; CUCI, AICI3 HNO, H2SO4 D HNO,, H2SO4 сн. Br H F SO, H2SO4 CO, CO, A-...
Hello, Would you please be able to answer this question number 1 please, I am having...
Hello,
Would you please be able to answer this question number 1
please, I am having a hard time understanding what is going on. Can
you please write it out in detail how you get the answers you did,
that way I can understand the thought process to answering a
question like this.
Thank you
1) (27 points) Give the structures of compounds A through I in the following series of reactions CH3 Brą, light CI Brą, AIBr; B AICI,...
Which set of reagents will accomplish the following transformation? COOH NH Br A) B) C) 1)...
Which set of reagents will accomplish the following transformation? COOH NH Br A) B) C) 1) CH;CI / AICI 2) Br2/FeBrz 3) Conc. KMnO4 OH, A. then H30 4) Cl2/AICI; 5) HNO3 H2SO4 6) Sn/HCI 1) CH3C1 / AICI 2) Conc KMnO4 OH, A, then H30* 3) HNO; / H2SO4 4) Sn HCI 5) Bry/FeBrz 6) C12/AICI: 1) CH,CI/AICI: 2) Bry/FeBrz 3) Cly/AICI: 4) Conc. KMnO OH, Athen H30 5) HNO3 /H SO. 6) Sn/HCI B) D) 1) HNO; H2SO4...
o GO 34. Aryl diazonium ions are formed from anilines reacted with: A. HNO, B. HNO3,...
o GO 34. Aryl diazonium ions are formed from anilines reacted with: A. HNO, B. HNO3, H2SO4 C. H2NNH, KOH D. NaNO, HCI 35. Starting with phthalic anhydride, which other reagents are needed for the Gabriel amine synthesis?: ? A. NH3, A/KOH, 1-pentyl-Br /H2NNH2 NH2 B. KOH, NH3 /LDA, 1-pentanol /NaOH C. NBS, Br, A/HCI, pentanamide / NaNO2, HCI D. NH3, HCI / NaH, 1-penty-CI/ KCN 36. Select the final product for the multi-step sequence indicated below: NHACCI EICI NaNO2...
Ph cyclopropene HF CH h) OH 1. POCICH.Ch 2. Pri 3 NH4Cl ag) 1.) 1. Li/THE...
Ph cyclopropene HF CH h) OH 1. POCICH.Ch 2. Pri 3 NH4Cl ag) 1.) 1. Li/THE 2.CO 3.NH.CH HNO k.) NH 1. HNO (aq) 2. NaSCH CH.CH AICI, 3-chloro-2-methylpentane m.) 1.Pr.CI. AICI 2. NBS, CCU. n) -OH XS H.CO acetone он 0.) OH XS Bobbit's SiO, CH.CH -OH 1. Ch. AICI 2 NaOH, 30 C 4,000 psi 3. HCI 9.) SCH 2Na, ETOH, NH, r.) 1. LIETO 2. oxirane 3. H,00 1.2 PY-MOBI OMe 2. NHCl(aq) t.) 1. Cl/ Feer...
1. please check what is wrong. Thank you! Determine the product formed when each compound is treated with...
1. please check what is wrong. Thank you!
Determine the product formed when each compound is treated with Br2 and FeBr3. Drag the atom labels to their appropriate positions. CN Atom labels H H Br Br2 A. FeBr Br H OH OH Br Br. Br2 FeBr3 H H Br Br H Br2 FeBr H1 H Reset T Rank the compounds in each group in order of decreasing reactivity in electrophilic aromatic substitution. CI Decreasing reactivity Rank the compounds in each...
a.) H H_Cro acetone b.) 1. XS KMnO,/KOH/HOIA 2.H30* c.) ni XS NaBH,, H,0 H OH...
a.) H H_Cro acetone b.) 1. XS KMnO,/KOH/HOIA 2.H30* c.) ni XS NaBH,, H,0 H OH d.) o 1. XS LAIH/THF/-78 °C 2. H20 H OH e.) NaNH / lig NH3 f.) Br 1. Mg/THE 2. CO2 3. H30 9.) Ph Ph cyclopropene HF CH h.) OH 1. PCCICH.CH 2. Pri 3. N,Cag) 1. LITHF 2.CO 3. NH.Ca) HNO, NH 1. HNO () 2. NaSCH CH.CH AICI, 3-chloro-2-methylpentane m.) 1.Pr.CI. AICI 2. NBS, CCH n.) OH XS H.COM acetone OH...
Using the list, propose the forward synthesis of the retrosynthesis shown below (and number of steps...
Using the list, propose the forward synthesis of the retrosynthesis shown below (and number of steps can be used, so long as they get to the desired product in as high a regioselectivity as possible). Please report your answer by typing the letters/symbols sequentially, A. PH. Br, KotBu, PhMe, 25 °C L. NaOH, H20, 160 °C B. CuBr 0 °C M. H2O, Dilute H2SO4, 100°C C. Cu20, Cu(NO3)2, H20.0°C N. HNO3, H2SO4, 60 °C D. CuCN, 0 °C E. SO3,...
Please help with these practices. Which undergoes the fastest
electrophilic substitution with Br2 or AlBr3?
Which substrate undergoes the most rapid electrophilic
substitution with HNO3/H2SO4?
Which reaction sequence results in this?
What is the major product for the reaction?
CH3 Оснз осна осна Br Б) с) d) NO2 осна осна OCH2CH3 OCH2CH3 H2C a) b) c) d) CH3 SO3H NO2 SO3H OCH3 Br OCH3 CI a) SO3 H2SO4 HNO3 H2SO4 Pd(OAC)2 AICI: (HO)2B OCH3 Br2 b) HNO3 H2SO4 SO3 H2SO4...
Draw the product(s) of the following reactions HNO,/H2SO а. Br b. AICI он So/H2SO C. Он Br/FeBr3 d. HNO3/H2SO4 Br e. OCH3 H3CO. f. AICI OCH3 но g. AICI NO3 Bro/FeBr3 h.
Give the product structures throughout the scheme, from A to I.
Follow the series of reactions.
Show product of this nucleophilic aromatic substitution
reaction.
Provide how a Diels Alder reaction would perform on this
compound.
Thanks so much
1) (27 points) Give the structures of compounds A through I in the following series of reactions CHE Brz, light CI Brz, AIBry AICI CO, HCI; CUCI, AICI3 HNO, H2SO4 D HNO,, H2SO4 сн. Br H F SO, H2SO4 CO, CO, A-...
Hello,
Would you please be able to answer this question number 1
please, I am having a hard time understanding what is going on. Can
you please write it out in detail how you get the answers you did,
that way I can understand the thought process to answering a
question like this.
Thank you
1) (27 points) Give the structures of compounds A through I in the following series of reactions CH3 Brą, light CI Brą, AIBr; B AICI,...
Which set of reagents will accomplish the following transformation? COOH NH Br A) B) C) 1) CH;CI / AICI 2) Br2/FeBrz 3) Conc. KMnO4 OH, A. then H30 4) Cl2/AICI; 5) HNO3 H2SO4 6) Sn/HCI 1) CH3C1 / AICI 2) Conc KMnO4 OH, A, then H30* 3) HNO; / H2SO4 4) Sn HCI 5) Bry/FeBrz 6) C12/AICI: 1) CH,CI/AICI: 2) Bry/FeBrz 3) Cly/AICI: 4) Conc. KMnO OH, Athen H30 5) HNO3 /H SO. 6) Sn/HCI B) D) 1) HNO; H2SO4...
o GO 34. Aryl diazonium ions are formed from anilines reacted with: A. HNO, B. HNO3, H2SO4 C. H2NNH, KOH D. NaNO, HCI 35. Starting with phthalic anhydride, which other reagents are needed for the Gabriel amine synthesis?: ? A. NH3, A/KOH, 1-pentyl-Br /H2NNH2 NH2 B. KOH, NH3 /LDA, 1-pentanol /NaOH C. NBS, Br, A/HCI, pentanamide / NaNO2, HCI D. NH3, HCI / NaH, 1-penty-CI/ KCN 36. Select the final product for the multi-step sequence indicated below: NHACCI EICI NaNO2...
Ph cyclopropene HF CH h) OH 1. POCICH.Ch 2. Pri 3 NH4Cl ag) 1.) 1. Li/THE 2.CO 3.NH.CH HNO k.) NH 1. HNO (aq) 2. NaSCH CH.CH AICI, 3-chloro-2-methylpentane m.) 1.Pr.CI. AICI 2. NBS, CCU. n) -OH XS H.CO acetone он 0.) OH XS Bobbit's SiO, CH.CH -OH 1. Ch. AICI 2 NaOH, 30 C 4,000 psi 3. HCI 9.) SCH 2Na, ETOH, NH, r.) 1. LIETO 2. oxirane 3. H,00 1.2 PY-MOBI OMe 2. NHCl(aq) t.) 1. Cl/ Feer...
1. please check what is wrong. Thank you!
Determine the product formed when each compound is treated with Br2 and FeBr3. Drag the atom labels to their appropriate positions. CN Atom labels H H Br Br2 A. FeBr Br H OH OH Br Br. Br2 FeBr3 H H Br Br H Br2 FeBr H1 H Reset T Rank the compounds in each group in order of decreasing reactivity in electrophilic aromatic substitution. CI Decreasing reactivity Rank the compounds in each...
a.) H H_Cro acetone b.) 1. XS KMnO,/KOH/HOIA 2.H30* c.) ni XS NaBH,, H,0 H OH d.) o 1. XS LAIH/THF/-78 °C 2. H20 H OH e.) NaNH / lig NH3 f.) Br 1. Mg/THE 2. CO2 3. H30 9.) Ph Ph cyclopropene HF CH h.) OH 1. PCCICH.CH 2. Pri 3. N,Cag) 1. LITHF 2.CO 3. NH.Ca) HNO, NH 1. HNO () 2. NaSCH CH.CH AICI, 3-chloro-2-methylpentane m.) 1.Pr.CI. AICI 2. NBS, CCH n.) OH XS H.COM acetone OH...
Using the list, propose the forward synthesis of the retrosynthesis shown below (and number of steps can be used, so long as they get to the desired product in as high a regioselectivity as possible). Please report your answer by typing the letters/symbols sequentially, A. PH. Br, KotBu, PhMe, 25 °C L. NaOH, H20, 160 °C B. CuBr 0 °C M. H2O, Dilute H2SO4, 100°C C. Cu20, Cu(NO3)2, H20.0°C N. HNO3, H2SO4, 60 °C D. CuCN, 0 °C E. SO3,...
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