(Wade Ch. 5) - Attempt 1 Chirality and the R,S System of Nomenclature www. Classify the following pair of molecules as enantiomers or diastereomers Drag the appropriate items to their respective bins. View Available Hint(s) Structures and I Sevdtures ill and IV Suctures and H H CHO OH OH CH₂OH Suctures and V CHO НО -H н -OH CH₂OH П СНО н OH HO-H CH.OH Ш feset Dracaens and V СНО HO -Я но-н CH₂OH Fely IV
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.
Please explain each
![<PS No. 09-(Wade Ch. 5)-Attempt 1
Chirality and the R,S System of Nomenclature
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Classify the following pair of molecules as enantiomers or diastereomers
Drag the appropriate items to their respective bins.
View Available Hint(s)
Structures and I Stuctures ill and TV Saructures and
Enantiomers
CHO
СНО
-ОН но-н
H-OH
CH₂OH
1
Sructures and V
Diastereomers
HOH
CH OH
П
Dructures and
сно
сно
н-он нон
HO-H
но-н
CH.OIL
CH OH
feat help
ructures and V
IV](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2Fec9523be-5f6c-46bc-84ca-9af77089f748%2Ffcb9ff17-1395-403e-891b-c6a9402ff6a2%2Fztvhs4e_processed.jpeg&w=3840&q=75)
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