Homework Answers
The most appropriate reagent will be option A TsCl, Et3N. Treatment of alcohol with tosyl chloride (TsCl) in presence of base will produce the given sulfonate ester. A base is required for this reaction and triethyl amine is the base here which is supplied to neutralize the produced HCl as side product. This is a substitution reaction where O-H bond substituted by O-S bond and Et3N will speed up the forward reaction by HCl neutralization.
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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 -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
Choose the most appropriate reagent(s) for the conversion of propyne and 2-methyl-1-tosyloxypropane to 5-methyl-2-hexyne. 1. reagent(s)...
Choose the most appropriate reagent(s) for the conversion of propyne and 2-methyl-1-tosyloxypropane to 5-methyl-2-hexyne. 1. reagent(s) :a 2. OTS TSCI, Et3N он NaNH2, NH3 3NaOH, H20 H2SO4 KOCH2CH3, HOCH2CH3 NH3
Choose the best option for the precursor to the tosylate derivative of 2-methyl-1-propanol. CH3 CH3 OTs...
Choose the best option for the precursor to the tosylate derivative of 2-methyl-1-propanol. CH3 CH3 OTs он он
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
what would be the reagent? Part 7 out of 8 Choose the most appropriate reagent(s) for...
what would be the reagent?
Part 7 out of 8 Choose the most appropriate reagent(s) for the conversion of the cis-epoxide intermediate to the target molecule. H2, Lindar catalyst CH3CO3H OH reagent(s) HOH A H,O, H,SO H,O, HBO CH,0 D 1.03 2. CH_SCH @ H20, HCI 2 attempts left 2 atempts et Check my work Next part
Choose the most appropriate reagent(s) for conversion of methyl bromide to methylmagnesium bromide. он reagent(s) 3Mg(OCH3)2,...
Choose the most appropriate reagent(s) for conversion of methyl bromide to methylmagnesium bromide. он reagent(s) 3Mg(OCH3)2, diethyl ether C Mg dicthyl ether O MgS04, H20 MgBr2, diethyl ether
Choose the most appropriate reagent(s) for the conversion of benzyl alcohol to benzaldehyde. OH H reagent(s)...
Choose the most appropriate reagent(s) for the conversion of benzyl alcohol to benzaldehyde. OH H reagent(s) H OH H CI
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
Design a synthesis of (Z) 5-methyl-2-hexene from propyne and 2-methyl-1-propanol. H -CH3 and OH Part 1...
Design a synthesis of (Z) 5-methyl-2-hexene from propyne and 2-methyl-1-propanol. H -CH3 and OH Part 1 Choose the best option for the immediate precursor to (Z) 5-methyl-2-hexene. CH Br Br This alkyne can be converted to (z 5-methyl-2-hexene in one step. Part 2 out of 9 Choose the best option for the nucleophile precursor to 5-methyl-2-hexyne. CH3
Question 4: Starting with 2-methyl-1-propanol, draw the organic product formed when treated with the following reagents:...
Question 4: Starting with 2-methyl-1-propanol, draw the organic product formed when treated with the following reagents: OH 2-methyl-1-propanol a) H.SO,, heat HCI c) 1) TsCl, py PBr 2) NaSH
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
Choose the most appropriate reagent(s) for the conversion of propyne and 2-methyl-1-tosyloxypropane to 5-methyl-2-hexyne. 1. reagent(s) :a 2. OTS TSCI, Et3N он NaNH2, NH3 3NaOH, H20 H2SO4 KOCH2CH3, HOCH2CH3 NH3
Choose the best option for the precursor to the tosylate derivative of 2-methyl-1-propanol. CH3 CH3 OTs он он
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
what would be the reagent?
Part 7 out of 8 Choose the most appropriate reagent(s) for the conversion of the cis-epoxide intermediate to the target molecule. H2, Lindar catalyst CH3CO3H OH reagent(s) HOH A H,O, H,SO H,O, HBO CH,0 D 1.03 2. CH_SCH @ H20, HCI 2 attempts left 2 atempts et Check my work Next part
Choose the most appropriate reagent(s) for conversion of methyl bromide to methylmagnesium bromide. он reagent(s) 3Mg(OCH3)2, diethyl ether C Mg dicthyl ether O MgS04, H20 MgBr2, diethyl ether
Choose the most appropriate reagent(s) for the conversion of benzyl alcohol to benzaldehyde. OH H reagent(s) H OH H CI
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
Design a synthesis of (Z) 5-methyl-2-hexene from propyne and 2-methyl-1-propanol. H -CH3 and OH Part 1 Choose the best option for the immediate precursor to (Z) 5-methyl-2-hexene. CH Br Br This alkyne can be converted to (z 5-methyl-2-hexene in one step. Part 2 out of 9 Choose the best option for the nucleophile precursor to 5-methyl-2-hexyne. CH3
Question 4: Starting with 2-methyl-1-propanol, draw the organic product formed when treated with the following reagents: OH 2-methyl-1-propanol a) H.SO,, heat HCI c) 1) TsCl, py PBr 2) NaSH
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