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Can ONLY use CO2 and CH3CN for carbon sources
20.71 Using acetonitrile (CH3CN) and CO2 as...
20.71 Using acetonitrile (CH3CN) and CO2 as your only sources of carbon atoms, identify how you...
20.71 Using acetonitrile (CH3CN) and CO2 as your only sources of carbon atoms, identify how you could prepare each of the following compounds: DODO OHROZOOH OH ОН (d)
Q1: Q2: Find the ΔHreaction Draw Lewis structures for the acetonitrile molecule (CH3CN), the methylamine molecule...
Q1:
Q2:
Find the ΔHreaction
Draw Lewis structures for the acetonitrile molecule (CH3CN), the methylamine molecule (CH3NH2), and the methanimine molecule (CH2NH) in the window below, and then answer the questions that follow, based on your drawings. Draw one structure per sketcher box. Separate added sketchers with + signs from the dropdown menu CP ChemDoodle What is the bond order of the carbon- nitrogen bond in the acetonitrile molecule?(enter a number) Which species has the shortest carbon-nitrogen bond, CH3CN, CH3NH2,...
2a and 2c please Using ethyne and/or methyl halides as your only sources of carbon, propose...
2a and 2c please
Using ethyne and/or methyl halides as your only sources of carbon, propose a synthesis of the following. compounds.
Using benzene, acetylene, dimethyl malonate, pyrrolidine (all other amines must be made from these other sources), CO2, CN ethylene oxide and/or monofunctional alcohols of 5 C or less as your sources...
Using benzene, acetylene, dimethyl malonate, pyrrolidine (all other amines must be made from these other sources), CO2, CN ethylene oxide and/or monofunctional alcohols of 5 C or less as your sources of carbon to be incorporated into the molecules, show how your 3 problems could be synthesized (see list below, and the attachment). Try to use reactions from the indicated chapters if you can. Please upload your work (prefer as pdf) as an attachment to assignment. Due by final (5/2)....
6. Using 4-nitrotoluene, sodium cyanide and carbon dioxide as the only sources of carbon, show how...
6. Using 4-nitrotoluene, sodium cyanide and carbon dioxide as the only sources of carbon, show how you would prepare; a. 4-nitrobenzoic anhydride. b. 4-nitrophenylacetic acid. Give two possible synthetic routes.
6. Devise a synthesis of molecule 1 using compound only sources of carbons. You can use any appropriate orga ecule...
6. Devise a synthesis of molecule 1 using compound only sources of carbons. You can use any appropriate orga ecule 1 using compounds ABC and D compounds A Band C are your ons You can use any appropriate organometallic and inorganic reagents as long des are typically hey are relevant to your synthesis Show all your steps clearly Recal Aldehydes are t more reactive that ketones.
Using methyl iodide, CH3I, and sodium acetylide as the sources of carbon atoms, show how to synthesize meso-2,3-dibromob...
Using methyl iodide, CH3I, and sodium acetylide as
the sources of carbon atoms, show how to synthesize
meso-2,3-dibromobutane. You may use any other needed reagents or
solvents, provided they do not supply carbon atoms to the final
product. About 5 steps are required. Please write out the formulas
of the reagents.
Free Response (10 pts each) Read instructions carefully and write out your answers in detail. 1. Using methyl iodide, CHI, and sodium acetylide, Nat:CECH, as the sources of carbon...
Show the steps for synthesis of Dimethylamine, labeling each step with the name of the reaction or reaction type and the reagents used. The only starting carbon sources you can use are alkanes with 3...
Show the steps for synthesis of Dimethylamine, labeling each
step with the name of the reaction or reaction type and the
reagents used. The only starting carbon sources you can use are
alkanes with 3 or fewer carbons, CO2, CN-, and CO. Thanks!
3 NI H 3
3 NI H 3
Show work and label reactions. Starting from benzonitrile and ethanol as your only sources of carbon...
Show work and label
reactions.
Starting from benzonitrile and ethanol as your only sources of carbon in the final molecule, synthesize the following using any reagents. -NH₂ ones OH он H₂o+ 6
ii. Provide a synthesis of the following the compound below, using 1-propanol and carbon dioxide as...
ii. Provide a synthesis of the following the compound below, using 1-propanol and carbon dioxide as your ONLY sources of carbon atoms. More than one step is required. You do NOT need to show the mechanism. You can use any other reagents that you desire. [6 marks]
20.71 Using acetonitrile (CH3CN) and CO2 as your only sources of carbon atoms, identify how you could prepare each of the following compounds: DODO OHROZOOH OH ОН (d)
Q1:
Q2:
Find the ΔHreaction
Draw Lewis structures for the acetonitrile molecule (CH3CN), the methylamine molecule (CH3NH2), and the methanimine molecule (CH2NH) in the window below, and then answer the questions that follow, based on your drawings. Draw one structure per sketcher box. Separate added sketchers with + signs from the dropdown menu CP ChemDoodle What is the bond order of the carbon- nitrogen bond in the acetonitrile molecule?(enter a number) Which species has the shortest carbon-nitrogen bond, CH3CN, CH3NH2,...
2a and 2c please
Using ethyne and/or methyl halides as your only sources of carbon, propose a synthesis of the following. compounds.
Using benzene, acetylene, dimethyl malonate, pyrrolidine (all other amines must be made from these other sources), CO2, CN ethylene oxide and/or monofunctional alcohols of 5 C or less as your sources of carbon to be incorporated into the molecules, show how your 3 problems could be synthesized (see list below, and the attachment). Try to use reactions from the indicated chapters if you can. Please upload your work (prefer as pdf) as an attachment to assignment. Due by final (5/2)....
6. Using 4-nitrotoluene, sodium cyanide and carbon dioxide as the only sources of carbon, show how you would prepare; a. 4-nitrobenzoic anhydride. b. 4-nitrophenylacetic acid. Give two possible synthetic routes.
6. Devise a synthesis of molecule 1 using compound only sources of carbons. You can use any appropriate orga ecule 1 using compounds ABC and D compounds A Band C are your ons You can use any appropriate organometallic and inorganic reagents as long des are typically hey are relevant to your synthesis Show all your steps clearly Recal Aldehydes are t more reactive that ketones.
Using methyl iodide, CH3I, and sodium acetylide as
the sources of carbon atoms, show how to synthesize
meso-2,3-dibromobutane. You may use any other needed reagents or
solvents, provided they do not supply carbon atoms to the final
product. About 5 steps are required. Please write out the formulas
of the reagents.
Free Response (10 pts each) Read instructions carefully and write out your answers in detail. 1. Using methyl iodide, CHI, and sodium acetylide, Nat:CECH, as the sources of carbon...
Show the steps for synthesis of Dimethylamine, labeling each
step with the name of the reaction or reaction type and the
reagents used. The only starting carbon sources you can use are
alkanes with 3 or fewer carbons, CO2, CN-, and CO. Thanks!
3 NI H 3
3 NI H 3
Show work and label
reactions.
Starting from benzonitrile and ethanol as your only sources of carbon in the final molecule, synthesize the following using any reagents. -NH₂ ones OH он H₂o+ 6
ii. Provide a synthesis of the following the compound below, using 1-propanol and carbon dioxide as your ONLY sources of carbon atoms. More than one step is required. You do NOT need to show the mechanism. You can use any other reagents that you desire. [6 marks]
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