The structure of (S)-2-fluorobutane is best r | vedclass

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(C) In $(S)-2$-fluorobutane,the chiral carbon $(C2)$ is attached to four different groups: $-F$,$-CH_2CH_3$,$-CH_3$,and $-H$.According to the Cahn-Ing

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(C) In $(S)-2$-fluorobutane,the chiral carbon $(C2)$ is attached to four different groups: $-F$,$-CH_2CH_3$,$-CH_3$,and $-H$.According to the Cahn-Ingold-Prelog $(CIP)$ priority rules,the priority order is $-F (1) > -CH_2CH_3 (2) > -CH_3 (3) > -H (4)$.The $(S)$ configuration indicates that the sequence of priorities $1$ $\rightarrow 2$ $\rightarrow 3$ is counter-clockwise when the lowest priority group $(-H)$ is oriented away from the observer.Option $(C)$ represents this specific stereoisomer.

The structure of $(S)-2$-fluorobutane is best represented by:

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