1. Formulate the potential product(s) of each of the following reactions. Write "no reaction" where appropriate. Determine the R/S designation for both starting materia and products if chiral center is present. Use boxes to provide your answer. Draw structures; DO NOT write molecular formula or chemical name as your answer. a) b) c) d) f) H₂O OSO₂CH3 -Br KBr acetone CH3CH₂ONa CH3CH₂OH H₂C H3C- KI acetone CH3 -OK CH3 CH3 -OH CH3 CH3CH₂ONa CH3CH₂OH
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.
![1. Formulate the potential product(s) of each of the following reactions. Write "no
reaction" where appropriate. Determine the R/S designation for both starting materials
and products if chiral center is present. Use boxes to provide your answer. Draw
structures; DO NOT write molecular formula or chemical name as your answer.
a)
b)
c)
Ⓡ
f)
H₂O
OSO₂CH3
-Br
CI
KBr
acetone
KI
CH3CH₂ONa
CH3CH₂OH
H₂C
acetone
CH3
-OK
CH3
CH3
H3C- -OH
CH3
CH3CH₂ONa
CH3CH₂OH](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2Ff46cd712-1d53-471c-8e4d-5e78c3c80932%2F35c8bfe1-c885-4d13-9a62-f7838a732dbe%2Fz79jyf_processed.png&w=3840&q=75)
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