Starting with ethene and 1-butanol as the only source of carbons, design a synthesis of butyl hex-2-enoate. (PLEASE ANSWER, I WILL RATE)
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Starting with ethene and 1-butanol as the only source of carbons, design a synthesis of butyl...
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...
(an oxiduse tertiary acohols. Design a synthesis of Z-3-hexen-1-ol from ethene as your only source of carbon (you may use any reagents you need, but all the carbon incorporated in the final molecule must originally have come from ethene).
Using only 1-butanol as your source of carbom, provide a
synthesis for the following compound.
Using only 1-butanol as your source of carbon, provide a synthesis for the following compound. You may use multiple equivalents of 1-butanol (use it more than once in the synthesis) Please use reactions that give the desired product as the major product Do not use the acetoacetic ester or malonic ester synthesis Show the product for each reaction step
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)
1. Devise a synthesis of 2-propylhexanenitrile (structure below) from butanol as the only starting material. CN
Design a synthesis of the following from starting materials
with 5 or fewer carbons. All materials used in the synthesis must
cost less than $5 per gram.
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).
3) Starting from a 2 carbon molecule of your choice (only caveat is 2 carbons. It can have anything else on it) design a synthesis of the compound below (4 points)
3) Starting from a 2 carbon molecule of your choice (only caveat is 2 carbons. It can have anything else on it) design a synthesis of the compound below (4 points)
Retrosynthetically design a synthesis from readily obtainable
starting compounds up to a max of 8 Carbons. Have atleast 1
carbon-carbon bond forming reaction for each synthesis. Show every
step, synthon and synthetic equivalents, and functional group
conversions (and additions, disconnections).
Also;
- Don’t need the forward reaction, but use all proper
conventions.
- Phenyl = Ph (six Carbons)
- The Disconnection needed is specified.
A)
B)
(a) 1,3 (Aldol) (b) 1,3
(a) 1,3 (Aldol)
(b) 1,3