Starting with propane as the only source of carbon and using only other INORGANIC reagents provide...
Starting with propane as the only source of carbon and using only other INORGANIC reagents provide a step- by- step synthesis of cis-hex-2-ene. Assume isomers can be separated (be regio- and stereo- specific).
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Starting with propane as the only source of carbon and using
only other INORGANIC reagents provide...
Provide step by step synthesis of the following compound starting from but-1-ene. Assume isomers can be...
Provide step by step synthesis of the following compound
starting from but-1-ene. Assume isomers can be separated (be regio-
and stereo- specific).
4. Provide step by step synthesis of the following compound starting from but-l-ene. Assume isomers can be separated (be regio- and stereo-specific).
1) Starting with methylcyclohexane and using any inorganc reagents, peroxides or alkoxides provide a step-by-step synthesis...
1) Starting with methylcyclohexane and using any inorganc
reagents, peroxides or alkoxides provide a step-by-step synthesis
of a cyclohexanone (ketone) and carbone dioxide. Show the
reactants/conditions for each step and the major organic product
molecule for each step. Assume isomers can be separated (be regio-
and stereospecific)
2)
2. Fill in the major product/s or reagents wherever appropriate. Be regio- and stereo-specific. NBS, hy
From propane as the only starting carbon source, synthesize 3-propoxyhexane. (please show synthesis of any organic reage...
From propane as the only starting carbon source, synthesize 3-propoxyhexane. (please show synthesis of any organic reagents which appear in the final product)
Starting from benzene or toluene as the only organic source plus other inorganic reagents, Show how...
Starting from benzene or toluene as the only organic source plus other inorganic reagents,
Show how the following can be synthesized
-CH2 -CHO HOZS
Complete the following synthesis using the shown starting material as the only source of carbon atoms...
Complete the following synthesis using the shown starting material as the only source of carbon atoms and any other necessary reagents. : 2. ?? starting material target Total Score:
Name 4. Starting with cyclohexene and acetylene as the only source of carbons, show a synthesis...
Name 4. Starting with cyclohexene and acetylene as the only source of carbons, show a synthesis of the compound below. 1. Show how you could make the given product from the given starting material. Show all steps. OH a CECH 2. Starting with acetylene and methyl bromide as your only source of carbons show a synthesis of cis-2-butene. 5. Prepare 2-methoxy-propanol from 1-bromo-propane. Show the steps and use any reagents you need. 3. Using acetylene and propyl bromide as your...
Using propyne (structure shown) as your only source of carbon atoms, design a synthesis of the...
Using propyne (structure shown) as your only source of carbon atoms, design a synthesis of the target molecule. You may use any organic or inorganic reagents you choose, but all the carbon atoms in the target must have come from propyne originally. Show the product of each step and the reagents needed for each step. Assume you have an unlimited supply of propyne.
2. Starting with ethanol as the only source of organic material and using any other reagents...
2. Starting with ethanol as the only source of organic material and using any other reagents that you desire, write equations to show the synthesis of (a) ethanoic acid, and (b) ethyl ethanoate. (4 marks)
1) Using 3-methyl-1-butene as the only source of carbon, and any other reagents, outline a synthesis...
1) Using 3-methyl-1-butene as the only source of carbon, and any other reagents, outline a synthesis for each compound a) 3 b) c)
(14) V. Starting from benzene and any other reagents you need, propose an efficient synthesis of th following compound. (10) VI. Devise a synthesis that will accomplish the following transformati...
(14) V. Starting from benzene and any other reagents you need, propose an efficient synthesis of th following compound. (10) VI. Devise a synthesis that will accomplish the following transformation in good yield. Use the given compounds as the only organic source of carbon atoms. You may use any common organic solvents as well as any needed inorganic reagents
(14) V. Starting from benzene and any other reagents you need, propose an efficient synthesis of th following compound. (10) VI....
Provide step by step synthesis of the following compound
starting from but-1-ene. Assume isomers can be separated (be regio-
and stereo- specific).
4. Provide step by step synthesis of the following compound starting from but-l-ene. Assume isomers can be separated (be regio- and stereo-specific).
1) Starting with methylcyclohexane and using any inorganc
reagents, peroxides or alkoxides provide a step-by-step synthesis
of a cyclohexanone (ketone) and carbone dioxide. Show the
reactants/conditions for each step and the major organic product
molecule for each step. Assume isomers can be separated (be regio-
and stereospecific)
2)
2. Fill in the major product/s or reagents wherever appropriate. Be regio- and stereo-specific. NBS, hy
Starting from benzene or toluene as the only organic source plus other inorganic reagents,
Show how the following can be synthesized
-CH2 -CHO HOZS
Complete the following synthesis using the shown starting material as the only source of carbon atoms and any other necessary reagents. : 2. ?? starting material target Total Score:
Name 4. Starting with cyclohexene and acetylene as the only source of carbons, show a synthesis of the compound below. 1. Show how you could make the given product from the given starting material. Show all steps. OH a CECH 2. Starting with acetylene and methyl bromide as your only source of carbons show a synthesis of cis-2-butene. 5. Prepare 2-methoxy-propanol from 1-bromo-propane. Show the steps and use any reagents you need. 3. Using acetylene and propyl bromide as your...
Using propyne (structure shown) as your only source of carbon atoms, design a synthesis of the target molecule. You may use any organic or inorganic reagents you choose, but all the carbon atoms in the target must have come from propyne originally. Show the product of each step and the reagents needed for each step. Assume you have an unlimited supply of propyne.
2. Starting with ethanol as the only source of organic material and using any other reagents that you desire, write equations to show the synthesis of (a) ethanoic acid, and (b) ethyl ethanoate. (4 marks)
1) Using 3-methyl-1-butene as the only source of carbon, and any other reagents, outline a synthesis for each compound a) 3 b) c)
(14) V. Starting from benzene and any other reagents you need, propose an efficient synthesis of th following compound. (10) VI. Devise a synthesis that will accomplish the following transformation in good yield. Use the given compounds as the only organic source of carbon atoms. You may use any common organic solvents as well as any needed inorganic reagents
(14) V. Starting from benzene and any other reagents you need, propose an efficient synthesis of th following compound. (10) VI....
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