Homework Answers
1) On further addition of H+ leads to removal of MgI with H.
2) Answer is c. Tetrahydrofuran is best solvent because it will not undergo Reaction with phenylmagnesium bromide whereas other solvent undergo reaction with it. Hence desired product is not obtained.
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Problem set Name 1. Please list all products and reagents in the box. (10 pts.) ︿сно...
Answer A-K please. (10 pts total) Give the structures for compounds/reagents A through K in the...
Answer A-K please.
(10 pts total) Give the structures for compounds/reagents A through K in the following road- map. 6-methylhept-1-yne D— SOCI, SOCI2 her G (CH3)2Culi (1) CH,MgBr in ether (2) H30+ CHICH), M&B (1) BOC (CH3)2CH(CH3 MgBr - (1) B (2) H30+ Na2Cr2O7 H2SO4 1,80m (1) K (2) H30+ (K KCN HCN (1) J OH (2) H30+. HO_ OH |
10. Complete the following synthesis by selecting from the list of 10 reagents below. Each reagent...
10. Complete the following synthesis by selecting from the list of 10 reagents below. Each reagent (or set of reagents) is labeled as a letter. In the answer box, simply place the order of reagents used as uppercase letters. For example, if your synthesis involves using reagent A followed by B, followed by C, and then D, your answer would be: ABCD. ? 'H Nang H2 1. LIAIH4 PCC OH HO Pd-C 2. H20 H* A B с D E...
please answer all parts Does 1-chlorobutane, an alkyl chloride, undergo a substitution reaction with the nucleophiles...
please answer all parts
Does 1-chlorobutane, an alkyl chloride, undergo a substitution reaction with the nucleophiles NaCl, NaBr, or Nal? Solubility data for each of these nucleophiles and the substrate is given in Table 1 below. Table 1: Solubility of Compounds in Various Solvents Compound Solvents in Which Soluble 1-chlorobutane Diethyl ether, hexanes, acetone, tetrahydrofuran NaCl Water, glycerol, ethylene glycol, formic acid NaBr Water, methanol Nal Water, ethanol, acetone 4. Write balanced chemical equations showing 1-chlorobutane undergoing a nucleophilic substitution...
please answer all parts Does 1-chlorobutane, an alkyl chloride, undergo a substitution reaction with the nucleophile...
please answer all parts
Does 1-chlorobutane, an alkyl chloride, undergo a substitution reaction with the nucleophiles NaCl, NaBr, or Nal? Solubility data for each of these nucleophiles and the substrate is given in Table 1 below. Table 1: Solubility of Compounds in Various Solvents Compound Solvents in Which Soluble 1-chlorobutane Diethyl ether, hexanes, acetone, tetrahydrofuran NaCl Water, glycerol, ethylene glycol, formic acid NaBr Water, methanol Nal Water, ethanol, acetone 4. Write balanced chemical equations showing 1-chlorobutane undergoing a nucleophilic substitution...
Complete the following synthesis by selecting from the list of 10 reagents below. Each reagent (or...
Complete the following synthesis by selecting from the list of 10 reagents below. Each reagent (or set of reagents) is labeled as a letter. In the answer box, simply place the order of reagents used as uppercase letters. For example, if your synthesis involves using reagent A followed by B and then c, and then D, your answer would be: ABCD. ubiri NaBH4 1. CHgMgBr 1. LiAlH4 PCC OH HO CH,OH 2. H20 2. H20 p-TSOH A B с D...
(10 pts) Show how you would accomplish the following synthetic conversion starting with ethanol as the...
(10 pts) Show how you would accomplish the following synthetic conversion starting with ethanol as the only source of organic carbon atoms. You may use any necessary inorganic reagent and solvent. Show all reaction steps, reagents and conditions used. OH ethanol 4-methylheptan-4-01
Extra Credit: There will be no partial credit. Answers must be correct. (10 pts) Show how...
Extra Credit: There will be no partial credit. Answers must be correct. (10 pts) Show how you would accomplish the following synthetic conversion starting with ethanol as the only source of organic carbon atoms. You may use any necessary inorganic reagent and solvent. Show all reaction steps, reagents and conditions used. OH ethanol OH 4-methylheptan-4-ol
Extra Credit: There will be no partial credit. Answers must be correct. (10 pts) Show how...
Extra Credit: There will be no partial credit. Answers must be correct. (10 pts) Show how you would accomplish the following synthetic conversion starting with ethanol as the only source of organic carbon atoms. You may use any necessary inorganic reagent and solvent. Show all reaction steps, reagents and conditions used. OH OH ethanol 4-methylheptan-4-ol
Extra Credit: There will be no partial credit. Answers must be correct. (10 pts) Show how...
Extra Credit: There will be no partial credit. Answers must be correct. (10 pts) Show how you would accomplish the following synthetic conversion starting with ethanol as the only source of organic carbon atoms. You may use any necessary inorganic reagent and solvent. Show all reaction steps, reagents and conditions used. OH ethanol OH 4-methylheptan-4-ol
Extra Credit: There will be no partial credit. Answers must be correct. (10 pts) Show how...
Extra Credit: There will be no partial credit. Answers must be correct. (10 pts) Show how you would accomplish the following synthetic conversion starting with ethanol as the only source of organic carbon atoms. You may use any necessary inorganic reagent and solvent. Show all reaction steps, reagents and conditions used. OH OH ethanol 4-methylheptan-4-ol
Answer A-K please.
(10 pts total) Give the structures for compounds/reagents A through K in the following road- map. 6-methylhept-1-yne D— SOCI, SOCI2 her G (CH3)2Culi (1) CH,MgBr in ether (2) H30+ CHICH), M&B (1) BOC (CH3)2CH(CH3 MgBr - (1) B (2) H30+ Na2Cr2O7 H2SO4 1,80m (1) K (2) H30+ (K KCN HCN (1) J OH (2) H30+. HO_ OH |
10. Complete the following synthesis by selecting from the list of 10 reagents below. Each reagent (or set of reagents) is labeled as a letter. In the answer box, simply place the order of reagents used as uppercase letters. For example, if your synthesis involves using reagent A followed by B, followed by C, and then D, your answer would be: ABCD. ? 'H Nang H2 1. LIAIH4 PCC OH HO Pd-C 2. H20 H* A B с D E...
please answer all parts
Does 1-chlorobutane, an alkyl chloride, undergo a substitution reaction with the nucleophiles NaCl, NaBr, or Nal? Solubility data for each of these nucleophiles and the substrate is given in Table 1 below. Table 1: Solubility of Compounds in Various Solvents Compound Solvents in Which Soluble 1-chlorobutane Diethyl ether, hexanes, acetone, tetrahydrofuran NaCl Water, glycerol, ethylene glycol, formic acid NaBr Water, methanol Nal Water, ethanol, acetone 4. Write balanced chemical equations showing 1-chlorobutane undergoing a nucleophilic substitution...
please answer all parts
Does 1-chlorobutane, an alkyl chloride, undergo a substitution reaction with the nucleophiles NaCl, NaBr, or Nal? Solubility data for each of these nucleophiles and the substrate is given in Table 1 below. Table 1: Solubility of Compounds in Various Solvents Compound Solvents in Which Soluble 1-chlorobutane Diethyl ether, hexanes, acetone, tetrahydrofuran NaCl Water, glycerol, ethylene glycol, formic acid NaBr Water, methanol Nal Water, ethanol, acetone 4. Write balanced chemical equations showing 1-chlorobutane undergoing a nucleophilic substitution...
Complete the following synthesis by selecting from the list of 10 reagents below. Each reagent (or set of reagents) is labeled as a letter. In the answer box, simply place the order of reagents used as uppercase letters. For example, if your synthesis involves using reagent A followed by B and then c, and then D, your answer would be: ABCD. ubiri NaBH4 1. CHgMgBr 1. LiAlH4 PCC OH HO CH,OH 2. H20 2. H20 p-TSOH A B с D...
(10 pts) Show how you would accomplish the following synthetic conversion starting with ethanol as the only source of organic carbon atoms. You may use any necessary inorganic reagent and solvent. Show all reaction steps, reagents and conditions used. OH ethanol 4-methylheptan-4-01
Extra Credit: There will be no partial credit. Answers must be correct. (10 pts) Show how you would accomplish the following synthetic conversion starting with ethanol as the only source of organic carbon atoms. You may use any necessary inorganic reagent and solvent. Show all reaction steps, reagents and conditions used. OH ethanol OH 4-methylheptan-4-ol
Extra Credit: There will be no partial credit. Answers must be correct. (10 pts) Show how you would accomplish the following synthetic conversion starting with ethanol as the only source of organic carbon atoms. You may use any necessary inorganic reagent and solvent. Show all reaction steps, reagents and conditions used. OH OH ethanol 4-methylheptan-4-ol
Extra Credit: There will be no partial credit. Answers must be correct. (10 pts) Show how you would accomplish the following synthetic conversion starting with ethanol as the only source of organic carbon atoms. You may use any necessary inorganic reagent and solvent. Show all reaction steps, reagents and conditions used. OH ethanol OH 4-methylheptan-4-ol
Extra Credit: There will be no partial credit. Answers must be correct. (10 pts) Show how you would accomplish the following synthetic conversion starting with ethanol as the only source of organic carbon atoms. You may use any necessary inorganic reagent and solvent. Show all reaction steps, reagents and conditions used. OH OH ethanol 4-methylheptan-4-ol
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