Show how each of the following compounds could be prepared using the given starting materials. Please Explain
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Show how each of the following compounds could be prepared using
the given starting materials. Please...
wing 6 Show how the following compounds could be prepared from the given starting materials. You...
wing 6 Show how the following compounds could be prepared from the given starting materials. You can use any necessary organic or inorganic reagents. NHCH -NH; CH OH OH ible or an inyersible reaction? Explain.
3. Propose reasonable syntheses of each of the following compounds from the given starting materials. You...
3. Propose reasonable syntheses of each of the following compounds from the given starting materials. You may use any other readily available alkyl halides, solvents and reagents as necessary. More than one step is necessary. Show all intermediates, reactions, reagents and conditions clearly. It is not necessary to show the mechanism. HCECH HCECH , X HCECH HC=CH M H OHC (30 marks)
Q 3. Show how each of the following compounds can be prepared from the given starting...
Q 3. Show how each of the following compounds can be prepared from the given starting materials using retrosynthetic analysis approach. a) Available starting materials (source of carbon) CO2Et OH OPMB TM BrCH2COOEt OH OH p-methoxybenzaldehyde
Q 2. Show how each of the following compounds can be prepared from the given starting...
Q 2. Show how each of the following compounds can be prepared from the given starting materials using retrosynthetic analysis approach. a) Available starting materials (source of carbon) H CH3NO2 Available starting materials (source of carbon)
Q 2. Show how each of the following compounds can be prepared from the given starting...
Q 2. Show how each of the following compounds can be prepared from the given starting materials using retrosynthetic analysis approach. O CO2Et *CO2Et Н
Q 1. Show how each of the following compounds can be prepared from the given starting...
Q 1. Show how each of the following compounds can be prepared from the given starting materials using retrosynthetic analysis approach. Available starting materials (source of carbon) a) .CO2Et CO2Et Ph Br CO2 or NaCN EtOH Ph CO2Et
6. How could the following compounds be prepared, using an alkene as one of the starting...
6. How could the following compounds be prepared, using an alkene as one of the starting materials? CI а. Br b.
Question 3 Show how you can synthesize the following compounds using the indicated starting materials and...
Question 3 Show how you can synthesize the following compounds using the indicated starting materials and any other necessary substances or reagents. (20 pts) A. CH COOH (starting from ortho-nitrotoluene) B. HN (starting from nitrobenzene)
Using the specified starting material and any other reagents, show how each of the following compounds...
Using the specified starting material and any other reagents,
show how each of the following compounds can be
prepared:
a) CH3-CH2-CH2-OH ---------> H3C-CC-H
B)CHCH------>
CH3-CH3-C-(Cl)2-CH3
c) HCCH -------->
CH2-CH2-CH(Br)-CH3
2. Starting with butane, show, using chemical equations, how you could prepare a. 2-bromobutane b. 1-bromobutane...
2. Starting with butane, show, using chemical equations, how you could prepare a. 2-bromobutane b. 1-bromobutane Note: For the following targets, you may also choose to begin with either 2-bromobutane or the 1-bromobutane as prepared above without repeatedly showing how you made these two compounds. Be sure to choose the best starting material for each job! c. 1-butene d. e. 3-methylheptane f. 5-methyl-3-heptyne
2. Starting with butane, show, using chemical equations, how you could prepare a. 2-bromobutane b. 1-bromobutane Note:...
wing 6 Show how the following compounds could be prepared from the given starting materials. You can use any necessary organic or inorganic reagents. NHCH -NH; CH OH OH ible or an inyersible reaction? Explain.
3. Propose reasonable syntheses of each of the following compounds from the given starting materials. You may use any other readily available alkyl halides, solvents and reagents as necessary. More than one step is necessary. Show all intermediates, reactions, reagents and conditions clearly. It is not necessary to show the mechanism. HCECH HCECH , X HCECH HC=CH M H OHC (30 marks)
Q 3. Show how each of the following compounds can be prepared from the given starting materials using retrosynthetic analysis approach. a) Available starting materials (source of carbon) CO2Et OH OPMB TM BrCH2COOEt OH OH p-methoxybenzaldehyde
Q 2. Show how each of the following compounds can be prepared from the given starting materials using retrosynthetic analysis approach. a) Available starting materials (source of carbon) H CH3NO2 Available starting materials (source of carbon)
Q 2. Show how each of the following compounds can be prepared from the given starting materials using retrosynthetic analysis approach. O CO2Et *CO2Et Н
Q 1. Show how each of the following compounds can be prepared from the given starting materials using retrosynthetic analysis approach. Available starting materials (source of carbon) a) .CO2Et CO2Et Ph Br CO2 or NaCN EtOH Ph CO2Et
6. How could the following compounds be prepared, using an alkene as one of the starting materials? CI а. Br b.
Question 3 Show how you can synthesize the following compounds using the indicated starting materials and any other necessary substances or reagents. (20 pts) A. CH COOH (starting from ortho-nitrotoluene) B. HN (starting from nitrobenzene)
Using the specified starting material and any other reagents,
show how each of the following compounds can be
prepared:
a) CH3-CH2-CH2-OH ---------> H3C-CC-H
B)CHCH------>
CH3-CH3-C-(Cl)2-CH3
c) HCCH -------->
CH2-CH2-CH(Br)-CH3
2. Starting with butane, show, using chemical equations, how you could prepare a. 2-bromobutane b. 1-bromobutane Note: For the following targets, you may also choose to begin with either 2-bromobutane or the 1-bromobutane as prepared above without repeatedly showing how you made these two compounds. Be sure to choose the best starting material for each job! c. 1-butene d. e. 3-methylheptane f. 5-methyl-3-heptyne
2. Starting with butane, show, using chemical equations, how you could prepare a. 2-bromobutane b. 1-bromobutane Note:...
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