Starting with a 4-carbon alcohol, a 4-carbon diol, and ethanol, design a synthesis for 3-ethyl-2-heptanone. (please show mechanism)
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Starting with a 4-carbon alcohol, a 4-carbon diol, and ethanol, design a synthesis for 3-ethyl-2-heptanone. (please...
Design a synthesis of ethyl 2-ethyl-3-oxohexanoate from alcohols containing 4 carbons or fewer. points COET alcohols containing 4 carbons or fewer Part 1 out of 9 Choose the best option for the precursor to the target molecule. Part 2 out of 9 19 Choose the best option for the carboxylic acid precursor to the intermediate ethyl butanoate. points TOET OET carboxylic acid alcohol oị © © carboxylic acid alcohol points ОН он о носH,CH, но Design a synthesis of ethyl...
IV. please plan a synthesis of 2-butanol using ethanol as the
only carbon source.
V. Suggest a reasonable mechanism to each of the following. (
on the pic)
value S pp IV. Please plan a synthesis of 2-butanol using ethanol as the only carbon source. Any reagents and/or solvents can be used. (9) Vaggest a reasonable medonsm to each o 根e dollowmy. Suggest a rtasonable mechont5 m 2)
Starting with 1-pentanol, design a synthesis for hexanoic anhydride. (Please show mechanism)
1) a) Draw 2-bromo-3-phenylpentanal. b) Draw 4-ethyl-6-methyl-3-heptanone.
Design a synthesis of the following compound using a alcohol as your starting material.
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)
Ethyl phenylacetate is a pleasant smelling compound used in perfumery. Propose a synthesis starting with benzene. Show all reagents and all intermediate structures. You do not need to show the mechanism. Assume ortho and para isomers can be separated. 3. Ethyl phenylacetate
Ethyl phenylacetate is a pleasant smelling compound used in perfumery. Propose a synthesis starting with benzene. Show all reagents and all intermediate structures. You do not need to show the mechanism. Assume ortho and para isomers can be...
Propose a synthesis of the following amine from ethanol. Ethanol
should be the only carbon source you use.
1.) Propose a synthesis of the following amine from ethanol. Ethanol should be the only carbon source you use. T OH 2) Propose a synthesis. I он 3) Propose a synthesis. I
what is the mechanism for 2-ethyl-3-hydroxy-hexanol? please show electron arrows. The starting materials are acetaldehyde, butanol, EtOH, KOH Thank you
1) Propose a synthesis of the following amine from ethanol. Ethanol should be the only carbon source you use. 2) Propose a synthesis. 3) Propose a synthesis. 1) PCC pn. 3)acid work up 5) 03 6) DMS 7)? 8)? 9) H/Ni 4) Propose a synthesis. 5) Name the following using IUPAC nomenclature.