Shown below is a proposed synthesis of the target molecule, starting with ethanol: Part 1 HO OH Reagent(s) ethanol Part 2 Reagent(s) The transformations above can be performed with some reagent or combination of the reagents listed below. Give the necessary reagents for each part in the correct order, as a string of letters (without spaces or punctuation, such as "EBF"). If there is more than one correct solution, provide just one answer. Part 1 Reagent(s): Part 2 Reagent(s): Last Step Reagent(s): A: NAOMe D: PCC or DMP Last Step Reagent(s) B: H+, -H₂O E: KMnO4, NaOH 1) BH3-THF; 2) H₂O2, NaOH F: conc. H₂SO4, heat C:
Reactive Intermediates
In chemistry, reactive intermediates are termed as short-lived, highly reactive atoms with high energy. They rapidly transform into stable particles during a chemical reaction. In specific cases, by means of matrix isolation and at low-temperature reactive intermediates can be isolated.
Hydride Shift
A hydride shift is a rearrangement of a hydrogen atom in a carbocation that occurs to make the molecule more stable. In organic chemistry, rearrangement of the carbocation is very easily seen. This rearrangement can be because of the movement of a carbocation to attain stability in the compound. Such structural reorganization movement is called a shift within molecules. After the shifting of carbocation over the different carbon then they form structural isomers of the previous existing molecule.
Vinylic Carbocation
A carbocation where the positive charge is on the alkene carbon is known as the vinyl carbocation or vinyl cation. The empirical formula for vinyl cation is C2H3+. In the vinyl carbocation, the positive charge is on the carbon atom with the double bond therefore it is sp hybridized. It is known to be a part of various reactions, for example, electrophilic addition of alkynes and solvolysis as well. It plays the role of a reactive intermediate in these reactions.
Cycloheptatrienyl Cation
It is an aromatic carbocation having a general formula, [C7 H7]+. It is also known as the aromatic tropylium ion. Its name is derived from the molecule tropine, which is a seven membered carbon atom ring. Cycloheptatriene or tropylidene was first synthesized from tropine.
Stability of Vinyl Carbocation
Carbocations are positively charged carbon atoms. It is also known as a carbonium ion.
Give the necessary reagents for each part in the correct order.
![Shown below is a proposed synthesis of the target molecule, starting with ethanol:
Part 1
HO
OH
Reagent(s)
ethanol
Part 2
Reagent(s)
The transformations above can be performed with some reagent or combination of the reagents listed below. Give the necessary
reagents for each part in the correct order, as a string of letters (without spaces or punctuation, such as "EBF"). If there is more
than one correct solution, provide just one answer.
Part 1 Reagent(s):
Part 2 Reagent(s):
Last Step Reagent(s):
A: NAOMe
D: PCC or DMP
Last Step
Reagent(s)
B: H+, -H₂O
E: KMnO4, NaOH
1) BH3-THF;
2) H₂O2, NaOH
F: conc. H₂SO4, heat
C:](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F9156f8b7-4f51-47ca-9489-d1b49d440928%2F18dd8779-4139-4046-b2b7-0c3024ebc4f0%2Frqzqn0k_processed.png&w=3840&q=75)
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