based on the reactivity of the reagent and to the
product conversion the possible reaction conditions are as
follows
show stepwise how you would prepare the following compounds
from the provided starting material and any other organic or
inorganic compound.
in order to have full credit you mush show all the reactions
conditions and the structure of your oroducts in each
transformation
(30 points) Show stepwise how would you prepare the following compounds from the provided starting material and any other organic or inorganic compound. In order to have full credit you must show all the reaction conditions and...
5. How would you synthesize the following compounds A-D starting from toluene? но toluene B C D
5. How would you synthesize the following compounds A-D starting from toluene? но toluene B C D
Organic Chemsitry
show stepwise how would you prepare the following compounds from the provided starting material and any other organic or inorganic compound. In order to have full credit you must show all of the reaction conditions and the structure of your products in each transformation 041 => Оet HO Eto Oet
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:...
10-2 Using acetylene as the starting material, show how you would synthesize the following compounds а) b) but-2-yne с) d)
how would you draw this?
d) 3-nitro-2-pentyne
5. (12 pts) How would you prepare the following compounds from the provided starting materials? You may use the given starting materials, any necessary inorganic reagents, and any carbon- containing compounds. (Hint: Each require more than one step!) ??? u осн. Но,
22. Show how you would make the target compounds on the right form the starting compounds on the left. Show reagents and conditions where appropriate, and the structures of important intermediate compounds. Do not show any (arrow pushing) mechanisms!!!! (8 points) NH2 3-Steps NH2 17. Show the products and give reaction mechanisms for the following, using curved arrows to indicate the flow of electrons between intermediates.
Show how you would synthesize the following compound starting
with acetylene and compounds containing no more than two carbon
atoms as organic starting material. You may use any additional
reagents you need
Br H H Br
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d. Prepare octane from 1-pentyne, indicate each needed
reagents.
e. Synthesize cis-2-hexene from 1-pentyne and an alkyl
halide.
f. Synthesize trans-2-hexene from 1-pentyne and an alkyl
halide.
Synthesize each compound from acetylene. You may use any other organic or inorganic reagents. a.