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Sequence rules to assign priorities to substituents
المؤلف:
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المصدر:
LibreTexts Project
الجزء والصفحة:
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6-7-2019
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Sequence rules to assign priorities to substituents
Before applying the R and S nomenclature to a stereocenter, the substituents must be prioritized according to the following rules:
Rule 1
First, examine at the atoms directly attached to the stereocenter of the compound. A substituent with a higher atomic number takes precedence over a substituent with a lower atomic number. Hydrogen is the lowest possible priority substituent, because it has the lowest atomic number.
- When dealing with isotopes, the atom with the higher atomic mass receives higher priority.
- When visualizing the molecule, the lowest priority substituent should always point away from the viewer (a dashed line indicates this). To understand how this works or looks, imagine that a clock and a pole. Attach the pole to the back of the clock, so that when when looking at the face of the clock the pole points away from the viewer in the same way the lowest priority substituent should point away.
- Then, draw an arrow from the highest priority atom to the 2nd highest priority atom to the 3rd highest priority atom. Because the 4th highest priority atom is placed in the back, the arrow should appear like it is going across the face of a clock. If it is going clockwise, then it is an R-enantiomer; If it is going counterclockwise, it is an S-enantiomer.
When looking at a problem with wedges and dashes, if the lowest priority atom is not on the dashed line pointing away, the molecule must be rotated.
Remember that
- Wedges indicate coming towards the viewer.
- Dashes indicate pointing away from the viewer.
Rule 2
If there are two substituents with equal rank, proceed along the two substituent chains until there is a point of difference. First, determine which of the chains has the first connection to an atom with the highest priority (the highest atomic number). That chain has the higher priority.
If the chains are similar, proceed down the chain, until a point of difference.
For example: an ethyl substituent takes priority over a methyl substituent. At the connectivity of the stereocenter, both have a carbon atom, which are equal in rank. Going down the chains, a methyl has only has hydrogen atoms attached to it, whereas the ethyl has another carbon atom. The carbon atom on the ethyl is the first point of difference and has a higher atomic number than hydrogen; therefore the ethyl takes priority over the methyl.
Rule 3
If a chain is connected to the same kind of atom twice or three times, check to see if the atom it is connected to has a greater atomic number than any of the atoms that the competing chain is connected to.
- If none of the atoms connected to the competing chain(s) at the same point has a greater atomic number: the chain bonded to the same atom multiple times has the greater priority
- If however, one of the atoms connected to the competing chain has a higher atomic number: that chain has the higher priority.
Example
A 1-methylethyl substituent takes precedence over an ethyl substituent. Connected to the first carbon atom, ethyl only has one other carbon, whereas the 1-methylethyl has two carbon atoms attached to the first; this is the first point of difference. Therefore, 1-methylethyl ranks higher in priority than ethyl, as shown below:
However:
Remember that being double or triple bonded to an atom means that the atom is connected to the same atom twice. In such a case, follow the same method as above.
Caution!!
Keep in mind that priority is determined by the first point of difference along the two similar substituent chains. After the first point of difference, the rest of the chain is irrelevant.
When looking for the first point of difference on similar substituent chains, one may encounter branching. If there is branching, choose the branch that is higher in priority. If the two substituents have similar branches, rank the elements within the branches until a point of difference.
After all your substituents have been prioritized in the correct manner, you can now name/label the molecule R or S.
- Put the lowest priority substituent in the back (dashed line).
- Proceed from 1 to 2 to 3. (it is helpful to draw or imagine an arcing arrow that goes from 1--> 2-->3)
- Determine if the direction from 1 to 2 to 3 clockwise or counterclockwise.
i) If it is clockwise it is R.
ii) if it is counterclockwise it is S.
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