Suggest a reasonable precursor for the synthesis of 1-chloro-3-ethylbenzene.
Suggest a reasonable precursor for the synthesis of 1-chloro-3-ethylbenzene.
Suggest a reasonable synthetic strategy for the synthesis of 3-ethyl-3-heptanol from methyl pentanoate, CH3CH2CH2CH2CO2CH3.
Design a synthesis of 1-chloro-2-propanol from 1-propanol.Choose the best option for the immediate precursor to the target molecule.An alkene can be used to introduce both an alcohol and a halide functional group to each of the carbons of the double bond in a controlled and predictable manner in one step. Choose the best option for the precursor needed to make the alkene.
Suggest a reasonable synthesis for the following compound using the given starting material and anything else you need. Question 3 (9 points) Suggest a reasonable synthesis for the following compound using the given starting material and anything else you need. (Hint: Show the intermediates, not only the conditions, for partial credit) ОН several steps
How would I do these two synthesis? Suggest a reasonable sequence of Reagents that could convert 2-cyclohexen-1-one into each compound: I am struggling with D and H. Sorry if the picture quality isn't great, the site won't allow any better. In H it is a =O and the starting compound has a double bond on the side.
3. Propose a synthesis of the molecule below starting with ethylbenzene. You can use any other reagents you want. (2 points) CH.CH COOH NO2
Starting with benzene, derive a synthesis of 1-chloro-2-nitrobenzene Cl NO2 Starting with benzene, derive a synthesis of 1-chloro-2-nitrobenzene Cl NO2
1. Draw the structures of the following compounds: a. 3-ethyl-4-methyl-2-hexene b.2-chloro-butyl acetate c. Ethylbenzene d. 2-methyl-3-pentanol e. 2-methylpropyl methyl ether 2. A) Distinguish between photodissociation and photoionization B) Use energy requirements of these two processes to explain why photodissociation of oxygen is more important than photoionization of oxygen at altitudes below about 90 km.
Please put all 6 steps. Design a synthesis of 2-bromo-1-chloro-4-nitrobenzene from benzene or any mono-substituted benzene. Cl Br benzene or any mono-substituted benzene NO2 Part 1 out of 6 Choose the best option for the immediate precursor to the target molecule. CI Br NO2
3. Propose a synthesis of the molecule below starting with ethylbenzene. You can use any other reagents you want. (2 points) COOH Br
Suggest a synthesis for the formation of 3-propyl-1-nitrobenzene from benzene.