Which reagents would you use to convert the aldehyde to the alcohol shown? Thank You!!
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Which reagents would you use to convert the aldehyde to the alcohol shown? Thank You!! Which reagents would you use to...
Which reagents will convert the alkyne shown into an aldehyde? OA. H2SO4, H20, HgSO4 B. 1....
Which reagents will convert the alkyne shown into an aldehyde? OA. H2SO4, H20, HgSO4 B. 1. BH3-THF 2. H2O2, OH- C. 1. H2SO4, H20 2. PCC, CH2Cl2 D. 1. Hg(OAC)2, H20 2. NaBH4, OH What reagents would use to carry out this synthesis? Br 1) n-PrCOCI, AICI: A. 2) Br2, FeBr3 3) NH2NH2, KOH, A 1) n-PrCOCI, AICI: B. 2) NH2NH2, KOH, A 3) Br2, FeBr3 1) Br2, FeBr3 OC. 2) n-BuCOCI, AICI: 3) NH2NH2, KOH, A 1) n-BuCI, AICI:...
?? 16. Which of the following reagents would promote non-Markovnikov addition to an alkene? a. 1....
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16. Which of the following reagents would promote non-Markovnikov addition to an alkene? a. 1. Hg(OAc)2, H20/THF, 2. NaBH4 b. KBr/KOH c. H30+ d. 1. BH3, THF 2. H202OH- 17. Halohydrin formation would be achieved by reacting an alkene with which of the following? a. b. c. d. Cl2 and water Water and methanol Os04 H2 and a catalyst 18. Reacting an alkene with 03 followed by Zn/H2O+ will create, a. Two carboxylic acids b. Two ketones c. One...
[References] From the table of available reagents select the one(s) you would use to convert cyclohexanone...
[References] From the table of available reagents select the one(s) you would use to convert cyclohexanone to the following compound: CH2CH2CO2H Use the minimum number of steps: from one to five are required. List reagents by letter in the order that they are used; example: fa. Reagents Available a. BH3, THF; followed by H2O2, OH g. Nat -CH(CO2C2H5) (from CH2(CO2C2H5)2 + Nat -OC2H5) b. Br2, CH3CO2H h. PBr3 c. HCN, KCN i. PhCH Br d. H307, heat j. Ph3P+- CH2...
6. Which series of reactions would best facilitate the following conversion? 1. KMa04 (ag) 2. HgrOAc)2...
6. Which series of reactions would best facilitate the following conversion? 1. KMa04 (ag) 2. HgrOAc)2 (ag) 3. NaBIL4OH b) 1. NaBH4 2. H3PO4' 4. H20H3o+ d) 1. NaBH4 e) I. Raney nickel 2. HBr (g) 3. Mg/etber 2. HyC-MgBr 3. H20/H30 7. What compound is prodaced when (R)-pentan-2-ol is treated with TsCI (aka TosCI) followed by Nal? a) sodium (R)-pent-3-oxide b) sodium (S)-pent-2-oxide c) (R)-2-iodopentane d) (S)-2-iodopentane e) none of the above 8. Which of the following reagents is...
Which of the following series of steps would most efficiently synthesize the target molecule from the...
Which of the following series of steps would most efficiently synthesize the target molecule from the given alcohol? HO Target 2 3 4 PCC 1. CH3MgBr 2. H20 H2SO4 Pd-o H2 1 2. 3 PCC 1. CH3CH2MgBr 2. H20 H2SO4 Pd-C H2 1 2 3 4 PCC 1. CH3MgBr 2. H2O H2SO4 Pd-C H2 0 1 2 3 4 PCC 1. CH3CH2MgBr 2. H₂O H2SO4 Pd-C H2 1 2 3 Na Cr2O7 H307 1. CH3 MgBr 2. H20 H2SO4 NaBH4...
(i) Carvone is the major constituent of spearmint oil. What products would you expect from the...
(i) Carvone is the major constituent of spearmint oil. What products would you expect from the reaction of carvone with the following reagents? Carvone CH3MrBr, then H30* (a) LIAIH4, then H30* (b) (c) H2, Pd (d) НОСН,СH2ОН, НСІ (е) CH;NH2
(i) Carvone is the major constituent of spearmint oil. What products would you expect from the reaction of carvone with the following reagents? Carvone CH3MrBr, then H30* (a) LIAIH4, then H30* (b) (c) H2, Pd (d) НОСН,СH2ОН, НСІ (е) CH;NH2
14) Which of the following reagents would react with a primary alcohol to produce an aldehyde as the final product?...
14) Which of the following reagents would react with a primary alcohol to produce an aldehyde as the final product? A) PCC B) H2SO4 C) H2Cr04 D) CH3MgBr, followed by HCI - 15) Which one of the following is not oxidized by K2Cr2O7 in H2SO4/H20? A) isobutyl alcohol B) tert-butyl alcohol C) sec-butyl alcohol D) n-butyl alcohol 16) Which of the following methods will NOT produce an alcohol as the product? A) hydroboration-oxidation of an alkene B) oxidation of an...
14) Which of the following reagents would react with a primary alcohol to produce an aldehyde as the final product?...
14) Which of the following reagents would react with a primary alcohol to produce an aldehyde as the final product? A) PCC B) H2SO4 C) H2C704 D) CH3MgBr, followed by HCI 15) - 15) Which one of the following is not oxidized by K2Cr2O7 in H2SO4/H20? A) isobutyl alcohol B) tert-butyl alcohol C) seo-butyl alcohol D) n-butyl alcohol 16) 16) Which of the following methods will NOT produce an alcohol as the product? A) hydroboration-oxidation of an alkene B) oxidation...
Select the reagents you would use to accomplish the syntheses shown below in no more than...
Select the reagents you would use to accomplish the syntheses shown below in no more than the number of steps specified. List the letters of the reagents in the order that they are used; example: fa. Reagents Available a. HBr b. PBr3 C. (CH3CH2CH2CH2)2Culi f. CH31 g. Hg(OAC)2, H2O, THF; then NaBH4 h. Cl2, light d. (CH3)2Culi I. KOH j. NBS (N-bromosuccinimide) e. BH3, THF; then H202, OH - он CH3 Use 2 steps: V - M Use 3 steps:
Identify the reagents to be used in the following synthetic schemes: (Specify the reagents you would use to carry o...
Identify the reagents to be used in the following synthetic schemes: (Specify the reagents you would use to carry out the conversion by using letters from the table. Write the letters in the order that they are used, c.g..abc.) Scheme 1: Scheme 2: a- -0- Reagents Available a. BH, THF then H2O2, OH h. NBS, CCL b. PBr3 HBO c. Mg. ether then H30 1. H2, Lindlar's catalyst d. (CH), Culi k. RCOOOH e. Brz I. O, then Zn, H30*...
Which reagents will convert the alkyne shown into an aldehyde? OA. H2SO4, H20, HgSO4 B. 1. BH3-THF 2. H2O2, OH- C. 1. H2SO4, H20 2. PCC, CH2Cl2 D. 1. Hg(OAC)2, H20 2. NaBH4, OH What reagents would use to carry out this synthesis? Br 1) n-PrCOCI, AICI: A. 2) Br2, FeBr3 3) NH2NH2, KOH, A 1) n-PrCOCI, AICI: B. 2) NH2NH2, KOH, A 3) Br2, FeBr3 1) Br2, FeBr3 OC. 2) n-BuCOCI, AICI: 3) NH2NH2, KOH, A 1) n-BuCI, AICI:...
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16. Which of the following reagents would promote non-Markovnikov addition to an alkene? a. 1. Hg(OAc)2, H20/THF, 2. NaBH4 b. KBr/KOH c. H30+ d. 1. BH3, THF 2. H202OH- 17. Halohydrin formation would be achieved by reacting an alkene with which of the following? a. b. c. d. Cl2 and water Water and methanol Os04 H2 and a catalyst 18. Reacting an alkene with 03 followed by Zn/H2O+ will create, a. Two carboxylic acids b. Two ketones c. One...
[References] From the table of available reagents select the one(s) you would use to convert cyclohexanone to the following compound: CH2CH2CO2H Use the minimum number of steps: from one to five are required. List reagents by letter in the order that they are used; example: fa. Reagents Available a. BH3, THF; followed by H2O2, OH g. Nat -CH(CO2C2H5) (from CH2(CO2C2H5)2 + Nat -OC2H5) b. Br2, CH3CO2H h. PBr3 c. HCN, KCN i. PhCH Br d. H307, heat j. Ph3P+- CH2...
6. Which series of reactions would best facilitate the following conversion? 1. KMa04 (ag) 2. HgrOAc)2 (ag) 3. NaBIL4OH b) 1. NaBH4 2. H3PO4' 4. H20H3o+ d) 1. NaBH4 e) I. Raney nickel 2. HBr (g) 3. Mg/etber 2. HyC-MgBr 3. H20/H30 7. What compound is prodaced when (R)-pentan-2-ol is treated with TsCI (aka TosCI) followed by Nal? a) sodium (R)-pent-3-oxide b) sodium (S)-pent-2-oxide c) (R)-2-iodopentane d) (S)-2-iodopentane e) none of the above 8. Which of the following reagents is...
Which of the following series of steps would most efficiently synthesize the target molecule from the given alcohol? HO Target 2 3 4 PCC 1. CH3MgBr 2. H20 H2SO4 Pd-o H2 1 2. 3 PCC 1. CH3CH2MgBr 2. H20 H2SO4 Pd-C H2 1 2 3 4 PCC 1. CH3MgBr 2. H2O H2SO4 Pd-C H2 0 1 2 3 4 PCC 1. CH3CH2MgBr 2. H₂O H2SO4 Pd-C H2 1 2 3 Na Cr2O7 H307 1. CH3 MgBr 2. H20 H2SO4 NaBH4...
(i) Carvone is the major constituent of spearmint oil. What products would you expect from the reaction of carvone with the following reagents? Carvone CH3MrBr, then H30* (a) LIAIH4, then H30* (b) (c) H2, Pd (d) НОСН,СH2ОН, НСІ (е) CH;NH2
(i) Carvone is the major constituent of spearmint oil. What products would you expect from the reaction of carvone with the following reagents? Carvone CH3MrBr, then H30* (a) LIAIH4, then H30* (b) (c) H2, Pd (d) НОСН,СH2ОН, НСІ (е) CH;NH2
14) Which of the following reagents would react with a primary alcohol to produce an aldehyde as the final product? A) PCC B) H2SO4 C) H2Cr04 D) CH3MgBr, followed by HCI - 15) Which one of the following is not oxidized by K2Cr2O7 in H2SO4/H20? A) isobutyl alcohol B) tert-butyl alcohol C) sec-butyl alcohol D) n-butyl alcohol 16) Which of the following methods will NOT produce an alcohol as the product? A) hydroboration-oxidation of an alkene B) oxidation of an...
14) Which of the following reagents would react with a primary alcohol to produce an aldehyde as the final product? A) PCC B) H2SO4 C) H2C704 D) CH3MgBr, followed by HCI 15) - 15) Which one of the following is not oxidized by K2Cr2O7 in H2SO4/H20? A) isobutyl alcohol B) tert-butyl alcohol C) seo-butyl alcohol D) n-butyl alcohol 16) 16) Which of the following methods will NOT produce an alcohol as the product? A) hydroboration-oxidation of an alkene B) oxidation...
Select the reagents you would use to accomplish the syntheses shown below in no more than the number of steps specified. List the letters of the reagents in the order that they are used; example: fa. Reagents Available a. HBr b. PBr3 C. (CH3CH2CH2CH2)2Culi f. CH31 g. Hg(OAC)2, H2O, THF; then NaBH4 h. Cl2, light d. (CH3)2Culi I. KOH j. NBS (N-bromosuccinimide) e. BH3, THF; then H202, OH - он CH3 Use 2 steps: V - M Use 3 steps:
Identify the reagents to be used in the following synthetic schemes: (Specify the reagents you would use to carry out the conversion by using letters from the table. Write the letters in the order that they are used, c.g..abc.) Scheme 1: Scheme 2: a- -0- Reagents Available a. BH, THF then H2O2, OH h. NBS, CCL b. PBr3 HBO c. Mg. ether then H30 1. H2, Lindlar's catalyst d. (CH), Culi k. RCOOOH e. Brz I. O, then Zn, H30*...
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