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weeeeeb [17]
3 years ago
7

Draw every stereoisomer for 1,2-difluoro-1,2-dimethylcyclopentane. Use wedge-and-dash bonds for the substituent groups, and be s

ure that they are drawn on the outside of the ring, adjacent to each other.

Chemistry
1 answer:
Blizzard [7]3 years ago
7 0

Answer:

See figure 1

Explanation:

In this question, we have to find first the <u>chiral carbons</u> on 1,2-difluoro-1,2-dimethylcyclopentane. Carbons 1 and 2. Then, using the <u>Cahn–Ingold–Prelog priority rules</u>. We can draw all the stereoisomers. If we have 2 chiral carbons we will have (2^n=2^2=4) <u>4 isomers</u>. With this in mind we can have the R,R isomer; the S,S isomer; the S,R isomer, and the R,S isomer. We have to remember that:

<u>Priority 1 = "F"</u>

<u>Priority 2= "C"</u>

<u>Priority 3= "CH2"</u>

<u>Priority 4 = "CH3"</u>

I hope it helps!

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