Curved arrows are used to illustrate the flow of electrons. Using the provided starting and product structures, draw the curved electron-pushing arrows for the following reaction or mechanistic steps. Be sure to account for all bond-breaking and bond-making steps. I³Q. Select to Add Arrows, s H=0,04 Select to Add Arrows; HCI, CH3CH₂OH HCI, CH3CH₂OH < OH ¡Select to Add Arrows HCI, CH3CH2OH Select to Add Arrows
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.
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HCI,
CH3CH2OH
••H
•6•H
Select to Add Arrows
HCI, CH3CH2OH
<
O
0:0.1
H
J
H.O.
¡Select to Add Arrows
HCI,
CH3CH₂OH
O•H
:0:
Problem 75 of 20
Please select a drawing or reagent from the question area](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F06f0fbe0-f317-435d-a2b5-90be2d5876f1%2F48d24bd4-6fcf-4473-9988-d43dc68a8fff%2F5slhw8q_processed.png&w=3840&q=75)
![↑
Curved arrows are used to illustrate the flow of electrons. Using
the provided starting and product structures, draw the curved
electron-pushing arrows for the following reaction or
mechanistic steps. Be sure to account for all bond-breaking
and bond-making steps.
OH
0.₁
:0:
H
Ho
Select to Add Arrows
OOH
I
¡Select to Add Arrows
HCI, CH3CH₂OH
HCI, CH3CH₂OH
>
OH
0.
¡Select to Add Arrows
HCI,
CH3CH2OH
H°
Select to Add Arrows
Problem 75 of 20
Please select a drawing or reagent from the question area](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F06f0fbe0-f317-435d-a2b5-90be2d5876f1%2F48d24bd4-6fcf-4473-9988-d43dc68a8fff%2F2s2sj83_processed.png&w=3840&q=75)
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